TRPV6 explained

TRPV6 is a membrane calcium (Ca²⁺) channel protein which is particularly involved in the first step in Ca²⁺absorption in the intestine.

Classification

Transient Receptor Potential Vanilloid subfamily member 6 (TRPV6) is an epithelial Ca²⁺ channel that belongs to the transient receptor potential family (TRP) of proteins.^[1] The TRP family is a group of channel proteins critical for ionic homeostasis and the perception of various physical and chemical stimuli. TRP channels can detect temperature, osmotic pressure, olfaction, taste, and mechanical forces.^[2] The human genome encodes for 28 TRP channels, which include six TRPV channels. The high Ca²⁺-selectivity of TRPV5 and TRPV6 makes these channels distinct from the other four TRPV channels (TRPV1-TRPV4).^[3] TRPV5 and TRPV6 are involved in Ca²⁺ transport, whereas TRPV1 through TRPV3 are heat sensors with different temperature threshold for activation, and TRPV4 is involved in sensing osmolarity.^{[4] [5]} Genetic defects in TRPV6 gene are linked to transient neonatal hyperparathyroidism and early-onset chronic pancreatitis. Dysregulation of TRPV6 is also involved in hypercalciuria, kidney stone formation, bone disorders, defects in keratinocyte differentiation, skeletal deformities, osteoarthritis, male sterility, Pendred syndrome, and certain sub-types of Cancer.

Identification

Peng et al identified TRPV6 in 1999 from rat duodenum in an effort to search for Ca²⁺ transporting proteins involved in Ca²⁺absorption.^[6] TRPV6 was also called calcium transport protein 1 (CaT1)^[7] initially although the names epithelial calcium channel 2 (ECaC2)^{[8] [9]} and CaT1-like (CaT-L)^[10] were also used in early studies to describe the channel. The human and mouse orthologs of TRPV6 were cloned by Peng et al and Weber et al, respectively. The name TRPV6 was confirmed in 2005.^[11]

Gene location, chromosomal location, and phylogeny

The human TRPV6 gene is located on chromosomal locus 7q33-34 close to its homolog TRPV5 on 7q35.^{[12] [13]} The TRPV6 gene in human encodes for 2906 bp-long mRNA. In contrast to most other proteins, which initiate translation with an AUG codon, TRPV6 translation is initiated by non-AUG-codon-mediated reading.^[14] TRPV6 protein bears a 40-a.a-long N-terminal extension in placenta and in some physiological settings in comparison to the annotated version of the protein used in biological studies. However, it is still to be determined whether the long version of the TRPV6 protein is the dominant form in different tissues.

Chromosomal location and identifiers

Species	Human	Rat	Mouse
Chromosomal location	7q33-q34	4q22	6B2
Annotated aa length	725	727	727
In vivo aa length^a	765	767	767
RefSeq nucleotide	NM_018646	NM_053686	NM_022413
RefSeq protein	NP_061116	NP_446138	NP_071858

^aTo be verified in different tissues.

It has been hypothesized that Trpv5 and Trpv6 genes were generated from a single ancestral gene by gene duplication events.^[15] Phylogenetic analysis has shown that TRPV6 paralogs in mammals, sauropsids, amphibians, and chondrichthyes arose out of independent duplication events in the ancestor of each group. It is speculated that two specialized Ca²⁺-selective Trpv homologs arose as an adaptation to achieve a greater degree of functional specialization for navigating distinct renal challenges of terrestrial animals. Two alleles of the TRPV6 gene have been identified in humans (originally noted as CaT-La and CaT-Lb). These alleles exhibit coupled polymorphisms generating two versions of the same gene.^[16] The polymorphisms give rise to an “ancestral variant” and a “derived variant” that differ in five bases and three amino acids. The ancestral allele codes for C197(157, in parentheses are annotated amino acid numbering), M418(378), and M721(681) whereas the derived allele codes for R197(157), V418 (378) and T721(681).^[17] The frequency of the ancestral TRPV6 allele varies across different population groups. It is hypothesized that selection pressures that could have changed TRPV6 allele distribution include changes in patterns of milk consumption, domestication of animals, change in ultraviolet light exposure due to trans-equatorial migration, genomic adaptations providing immune advantages to populations encountering new pathogens.^[18]

Tissue distribution

The TRPV6 protein is expressed in epithelial tissues such as the intestine, kidney, placenta, epididymis, and exocrine glands such as pancreas, prostate and salivary, sweat, and mammary glands.^{[19] [20]} TRPV6 protein expression in humans has been demonstrated in the esophagus, stomach, small intestine, colon, pancreas, mammary glands, ovary, thyroid, and prostate by immunohistochemistry approaches. TRPV6 expression mainly confines on the apical membrane of epithelial cells. In the intestine, the protein is expressed on the brush-border membrane of enterocyte.

Differences in the TRPV6 expression profile have been reported possibly due to variation in assay-dependent such primer design, hybridization probes, PCR vs. northern blotting, semi-quantitative PCR vs. RT-PCR, and antibodies used for immunodetection.^[21] TRPV6 expression profile is also influenced by age, gender, Ca²⁺ and vitamin D₃ levels in food, hormonal status, location within the tissue, cellular location, reproductive status, and weaning status (see Section Regulation).

In humans, TRPV6 transcripts have been detected in the placenta, pancreas, prostate cancer, and duodenum and the prostate by northern blotting; and in duodenum, jejunum, placenta, pancreas, testis, kidney, brain, and colon by semi-quantitative PCR. In rodents, TRPV6 expression has been validated in the duodenum, cecum, small intestine, colon, placenta, pancreas, prostate, and epididymis by Northern Blotting.^[22] In mouse, TRPV6 transcript abundance measured by RT-PCR is as follows: prostate > stomach, brain > lung > duodenum, cecum, heart, kidney, bone > colon > skeletal muscle > pancreas.^[23]

Data from Human Protein Atlas and RNA-Seq based suggest TRPV6 mRNA is low in most tissues except for the placenta, salivary gland, pancreas, and prostate.^[24] TRPV6 mRNA is expressed in the apical domain of murine osteoclasts of cortical bone.^{[25] [26]} Cortical and trabecular osteocytes do not express TRPV6 mRNA whereas osteoblasts show weak expression.^[27]

Structure and biophysical properties

Primary and secondary structure

Overall, four subunits of TRPV6 arrange to form a tetrameric channel displaying a four-fold symmetry.^[28] Beginning from N-terminus and moving towards the C-terminus of the protein, each TRPV6 polypeptide contains: an N-terminal helix, an ankyrin repeat domain (ARD) containing six ankyrin repeats, a β-hairpin structure linker domain made up two β-strands, a helix-turn-helix motif, a pre-SI helix, TM domain made up of six TM helices (S1 through S6), a pore-loop (also called P-loop), amphipathic TRP helix, C-terminal hook, and a six-residue β-strand (β3) (Figure 1).

Tertiary and quaternary structure

The TRPV6 channel protein displays four-fold symmetry and contains two main compartments: a 30 Å-tall transmembrane domain with a central ion channel pore and a ~70 Å-tall and a ~110 Å-wide intracellular skirt enclosing a 50 Å × 50 Å cavity wide cavity underneath the ion channel. The clustering of four TRPV6 subunits forms an aqueous pore exhibiting a fourfold symmetry (Figure 2). A pre-SI helix links the intracellular portion of the protein to the TM domain through a linker domain made up of β-hairpin structure and a helix-turn-helix motif. Helices S1 through S4 form a transmembrane helical bundle or TM domain that is inserted almost perpendicularly to the plane of the plasma membrane.

The pore module elements are made up of S5, S6, and the P-loop in TM domains. The pore module from each TRPV6 polypeptide participates in inter-subunit interactions to form a central ion pore (Figure 1). The pore-forming elements of each TRPV6 subunit also interact with S1-S4 domains of the adjacent polypeptide in a domain-swapped arrangement.^[29] Intersubunit interactions also occur between S1-S2 extracellular loops and S5-P and S6-P loops of the neighboring TRPV6 subunits. The conserved N-linked glycosylation site on the S1-S2 loop is required for by the Klotho-mediated activation.^[30] The intracellular skirt portion of the TRPV6 protein is mainly made up of the ankyrin repeats. The TRP domain is oriented parallel to the membrane and participates in hydrophobic interactions with the TM domain and the hydrophilic interactions in the intracellular skirt. The N-terminal helix, C-terminal hook, and β-sheets (formed by the β-hairpin structure in the linker domain) in the channel participates in intersubunit interactions with the ARDs to provides a framework for holding the elements of the intracellular skirt together.

Pore architecture and cation binding sites

The TRPV6 pore has four main elements, namely, the extracellular vestibule, a selectivity filter, a hydrophobic cavity, and a lower gate.^{[31] [32]} Facing the central lumen of the channel, a four-residue selectivity filter (⁵³⁸TIID⁵⁴¹) containing four Aspartate 541 (D541) side chains (one from each protomer) is critical for Ca²⁺ selectivity and other biophysical properties of the channel. This filter forms a negatively charged ring that discriminates between ions based on their size and charge. Mutations in the critical pore-forming residue of TRPV6 blocks Ca²⁺uptake, a strategy has been used to generate TRPV6 loss-of-function models to examine the role of the channel in animal physiology. Four different types of cation binding sites are thought to exist in the TRPV6 channel. Site 1 is located in the central pore and shares the same plane that is occupied by the key selective residues D541. Site 2 is thought to be present about 6-8 Å below Site 1 followed by Site 3 which is located in the central pore axis about 6.8 Å below Site 2. Site 2 and 3 are thought to interact with partially-hydrated to equatorially-hydrated Ca²⁺ ions. Finally, four symmetrical cation binding sites in the extracellular vestibule mediate the recruitment of cations towards the extracellular vestibule of TRPV6 and are referred to as recruitment sites.

Ion permeation

The conductance of TRPV6 for divalent cations follows the preference: Ca²⁺ > Ba²⁺ > Sr²⁺ > Mn². Intra-cellular Mg²⁺ inhibits TRPV6 and contributes to the strong inward rectification exhibited by the channel.^[33] TRPV6 uptake activity is inhibited by divalent Pb², Cu²⁺, Cd²⁺, Zn², Co²⁺, Fe²⁺, and trivalent cations La³⁺, Fe³⁺, Gd³⁺. The concentration of ions to achieve the inhibition ranges from 1 to 10 μM.^[34] The TRPV6 protein is constitutive with a single-channel conductance of 42-58 ps.^[35] At low Ca²⁺ concentrations, a single Ca²⁺ ion binds in the selectivity filter formed by D541 and permits Na⁺ permeation. At high Ca²⁺ concentration, Ca²⁺ permeation occurs by a knock-off mechanism that involves the formation of short-lived conformations involving binding of three Ca²⁺ ions to residue D541.

Channel gating

The conformational changes involved in channel opening are hinged around the residue Alanine 566 (A566) and occur in the pore-lining helix S6 (Figure 3). The upper portion of S6 helix undergoes an α-to-π helical transition which forces the lower portion of the helix to turn by 100 degrees and tilt away from the pore axis by 11 degrees. This conformational change moves the lower portion of the helix gating the pore and thereby widens the pore size. The conformational change alters the residues facing the pore axis and triggers the formation of new electrostatic bonds subunit and salt bridges that offset the high energetic cost of unfavorable α-to-π helical transition that occurs during channel opening.

Regulation by phosphatidylinositol 4,5-bisphosphate (PIP₂) and calmodulin (CaM)

The influx of Ca²⁺ inside the cell triggers negative feedback mechanisms to suppress TRPV6 activity and prevent Ca²⁺ overload. TRPV6 channel activity is regulated by the intracellular level of phospholipid phosphatidylinositol 4,5-bisphosphate (PIP₂) and interactions with Ca²⁺-Calmodulin (CaM) complex. The depletion of PIP₂ or CaM-binding inactivates TRPV6.^{[36] [37] [38] [39] [40]} The influx of Ca²⁺ in TRPV6 expressing cells activates phospholipase C (PLC) which in turn hydrolyzes PIP₂. Depletion in PIP₂ levels results in a decline in channel activity since most TRP channels require this lipid for activation. The lipid PIP₂ can override Ca²⁺-CaM-mediated inhibition of TRPV6. Overall, TRPV6 inactivation by calmodulin is orchestrated by a balance of intracellular Ca²⁺ and PIP₂ concentration.

Interacting proteins

Among 20+ TRPV6 interactors identified so far, the functional consequences of Ca²⁺-binding protein Calmodulin (CaM) and Glucuronidase Klotho have been most extensively characterized [36, 37, 41, 42].^{[41] [42]} Functional consequences of TRPV6 channel activation are summarized in the table below).^[43]

TRPV6 Interactors and their Functional Consequences

Interactor	Consequence
BSPRY	N/A
Calbindin-D28k	N/A
Calmodulin	Inhibition
Cyclophilin B	Activation
FYN	PO4lyation
I-MFA	N/A
Klotho	Activation, Glycosylation (Asn-357)
NHERF4	Activation
NIPSNAP1	Inhibition
NUMB	Inhibition
PTEN	N/A
PTP1B	DePO4lyation (Tyr-161 and Tyr-162)
RAB11A	Activation, Increase in Plasma membrane level
RGS2	N/A
RYR1	N/A
S100A10	Activation, Increase in Plasma membrane level
SRC	PO4lyation (Tyr-161, 162)
TRPC1	Retains in ER, Inhibition
TRPML3	N/A
TRPV5	Tetramer formation, New Channel creation

Abbreviations

Protein Interactor

BSPRY: B-Box and Spry Domain Containing Protein; FYN: Fyn Kinase Belonging Src Family of Kinases; I-MFA: Myo D Family Inhibitor; NHERF: Na Exchanger Regulatory Factor; NIPSNAP14-Nitrophenylphosphatase Domain and Non-Neuronal SNAP25-Like Protein Homolog 1; Numb: Drosophila mutation that removes most of the sensory neurons in the developing peripheral nervous system; PTP: Protein Tyrosine Phosphatase; Rab11a: Member RAS Oncogene Family; RGS2: Regulator Of G-Protein Signaling 2; RyR1: Ryanodine Receptor 1; TRPC1: Transient receptor potential canonical 1; TRPML3: Transient receptor potential Mucolipin-3.

Physiological functions

The Ca²⁺-selective channel proteins TRPV6 and TRPV5 cooperate to maintain calcium concentration in specific organs.^[44] TRPV6 functions as apical Ca²⁺ entry channels mediating transcellular transport of this ion in the intestine, placenta, and possibly some other exocrine organs. TRPV6 also plays important roles in maternal-fetal calcium transport,^[45] keratinocyte differentiation,^[46] and Ca²⁺ homeostasis in the endolymphatic system of the vestibular system,^{[47] [48]} and maintenance of male fertility.^{[49] [50]}

Ca²⁺ absorption in intestine

Two routes of Ca²⁺ absorption are recognized: paracellular transport and transcellular transport (see Figure 4).^[51] A high-Ca²⁺-diet favors paracellular transport of the ion across the length of the intestine allowing them to pass between the intercellular tight junctions that connect epithelial cells. In contrast under conditions when [Ca²⁺] in the lumen of the intestine is lower in comparison to its concentration in the plasma (e.g. during low dietary Ca²⁺), the transcellular pathway is required for adequate Ca²⁺ absorption. Three important steps in transcellular Ca²⁺ transport are recognized: cellular entry of Ca²⁺ ion on the apical side via TRPV6 (Step-1), the binding of Ca²⁺ ion with calbindin-D_9k (Step-2)_, and exit of Ca²⁺ from the basolateral side via the plasma membrane Ca²⁺ ATPase (PMCA1b). The hormone Vitamin D₃ (or 1,25(OH)₂D₃) plays an important role in TRPV6-mediated intestinal Ca²⁺ absorption).

Ca²⁺ reabsorption in the kidney

In contrast to the intestine, where TRPV6 is the gatekeeper of Ca²⁺ absorption, the transcellular reabsorption of this ion in the kidney occurs through TRPV5. Although TRPV5 is a recognized gatekeeper for transcellular reabsorption of Ca²⁺ ion in the kidney, TRPV6 knockout (KO) mice also struggle to concentrate their urine and display hypercalciuria.^[52] TRPV6 is known to co-localize with TRPV5 Calbindin-D_28K in apical domains of distal convoluted tubules and connecting tubules [20]. TRPV5 KO mice compensate for Ca²⁺ loss by increasing TRPV6 expression in the duodenum. Moreover, a recent study analyzing vitamin D responsive genes in ovine, canine and, equine kidney suggested that TRPV6, calD_9k/calD_28k, and PMCA could be the main pathways orchestrating transcellular Ca²⁺ transport in the kidney of sheep, dogs, and horses.^[53]

Maternal-fetal Ca²⁺ transport

TRPV6 plays an indispensable role in placental Ca²⁺ transport. Fetal bone mineralization peaks during late pregnancy. At this stage, fetal blood has a higher concentration of Ca²⁺ in comparison to maternal blood thereby creating conditions that require active transcellular transport of Ca²⁺ from mother to the fetus.^{[54] [55]} This process is very important since defects in placental transport of calcium can be precursors for Ca²⁺ deficiency syndromes and intrauterine growth restrictions.^[56] The expression of TRPV6 increases 14-fold during the last 4 days of the murine gestational period and coincides with the peak phase of fetal bone mineralization. The protein TRPV6 is abundantly expressed in the mammalian placental tissues.^{[57] [58] [59] [60]} Indeed, TRPV6 expression is ~1000-fold higher in comparison to TRPV5. In the placenta, TRPV6 is expressed in trophoblasts and syncytiotrophoblasts. In mice, TRPV6 mRNA and protein are expressed in the intraplacental yolk sac and the visceral layer of the extraplacental yolk sac. Most importantly, TRPV6 KO fetuses exhibit a 40% reduction in ⁴⁵Ca²⁺ transport activity and a dramatic decrease in the ash weight (a measure of fetal bone health). In humans, trophoblasts fluid shear stress (FSS) is known to induce a TRPV6-mediated Ca²⁺ influx and promote microvilli formation through a mechanism involving Ezrin and Akt-phosphorylation.^[61]

Epididymal Ca²⁺ regulation and implications on male fertility

The regulation of calcium concentration in the epididymal lumen is critical for sperm motility.^[62] TRPV6-mediated reduction of luminal Ca²⁺ concentration in the epididymis is critical for male fertility in mice. TRPV6 KO mice or mice expressing loss-of-function version of TRPV6 channel (Trpv6^D541A homozygous mice) have a severely impaired fertility. Mice expressing nonfunctional TRPV6 have a 10-fold higher concentration of Ca²⁺ in the epididymal lumen and Ca²⁺ uptake in this space is reduced by 7-to-8 folds. The increases Ca²⁺ ion in epididymal lumen concentration leads to significant defects in motility, fertilization capacity, and viability of sperms in TRPV6^D541A mice. It appears TRPV6 and chloride channel transmembrane manner 16 A (TMEM16A) act cooperatively to reduce the luminal concentration of Ca²⁺ in the epididymal lumen.^[63]

Bone health

Under conditions of sub-optimal dietary Ca²⁺, normal serum calcium levels in TRPV6 KO mice are maintained at the expense of bone.^{[64] [65]} TRPV6 plays an important role in osteoclasts but not in osteoblasts. In mice, TRPV6 depletion results in increased osteoclasts differentiation whereas TRPV5 is essential for proper osteoclastic bone resorption.

Keratinocyte differentiation

Keratinocytes differentiation is orchestrated by calcium switch, a process that entails an influx of Ca²⁺ in keratinocyte which induces broad transcriptional changes necessary for desmosome formation, stratification, and cornification.^[66] TRPV6 KO mice display thinner layers of stratum corneum and 20% of the mice also show alopecia and dermatitis. The silencing of TRPV6 impairs Ca²⁺-mediated differentiation of human primary keratinocytes and downregulates differentiation markers such as involucrin, transglutaminase-1, and cytokeratin-10. The hormone 1,25-dihydroxyvitamin-D3 upregulates TRPV6 in keratinocytes and triggers a Ca²⁺ influx. This in turn induces the expression of keratinocyte differentiation-specific pathways.

Role in the inner ear

The proteins TRPV5 and TRPV6 are expressed in several regions of the inner ear as well as in primary cultures of semicircular canal duct (SCCD) epithelium. Some studies have indicated that TRPV5 and TRPV6 are needed for lowering the Ca²⁺ concentration in the lumen of mammalian endolymph, a requirement that is essential for normal hearing and balance.

Uterine and placental expression of TRPV6 and implications in pregnancy

The endometrial and uterine expression of TRPV6 has been reported in mammals.^{[67] [68] [69]} The expression of TRPV6 in the uterus is thought to be hormonally regulated by 17β-estradiol and progesterone in rodents. In rodents, TRPV6 mRNA is expressed in the labyrinth and spongy zone as well as placenta-unattached areas of the uterus. The stage of pregnancy is an important regulator of TRPV6 expression. The downregulation of TRPV5/6 expression and a resulting decline in Ca²⁺ transport is thought to change the proliferative profile of human trophoblasts; a process which in turn is linked to the development of pre-eclampsia. This juxtaposition of TRPV6 expression and its stringent regulation by sex hormones during pregnancy suggest that the protein may be important for embryo implantation, however conclusive evidence for this connection does not exist.

Implications in Human Diseases

Transient Neonatal Hyperparathyroidism

Loss of TRPV6 in murine placenta severely impairs Ca²⁺ transport across trophoblast and reduces embryo growth, induces bone calcification, and impairs bone development. In humans, the insufficient maternal-fetal transport caused by pathogenic genomic variants of TRPV6 is thought to be a cause for skeletal defects observed in selected case reports of transient neonatal hyperparathyroidism (TNHP) cases. These variants are believed to compromise the plasma membrane localization of the protein. Exome sequencing of an infant with severe antenatal onset thoracic insufficiency with accompanying fetal skeletal abnormalities indicates the critical role of TRPV6 in maternal-fetal transport. The study indicated that compound heterozygous variants of TRPV6 result in severe undermineralization and severe dysplasia of the fetal skeleton.^{[70] [71] [72]}

Chronic Pancreatitis

Recent evidence indicates that naturally occurring TRPV6 loss of function variants predisposes certain demographics to chronic pancreatitis (CP) by dysregulating calcium homeostasis in the pancreatic cells.^{[73] [74]} Sequencing studies among chronic pancreatitis patients revealed the presence of 33 missense and 2 nonsense variants predisposed Japanese, German, and French patients to a higher risk of CP. Overall, these studies have shown that disease-inducing TRPV6 loss-of-function genomic variants are over-represented in German, French, Chinese, and Japanese CP patients in comparison to controls in their respective groups. The loss-of-function variants are believed to compromise calcium transport in the pancreas by act by either reducing the total protein level and/or compromising Ca²⁺ uptake activity by the channel.

Kidney Stone Formation

The role of TRPV6 in renal stone formation has been suggested through sequencing studies conducted on a cohort of 170 patients in Switzerland.^[75] The studies revealed that the frequency of TRPV6 gain-of-function haplotype is significantly higher in Ca^2+-stone formers (nephrolithiasis) in comparison to non-formers. The observed hypercalciuria phenotypes from animal studies and studies on TRPV6 single nucleotide polymorphisms (SNPs) suggest that TRPV6 haplotype could be an important risk factor for absorptive and renal hypercalciuria (kidney stones due to impaired intestinal absorption and renal re-absorption respectively). The lower incidence of kidney stone diseases in African-Americans and a relatively higher prevalence of ancestral haplotype suggest theory according to which this haplotype endows an advantage of increased Ca²⁺ reabsorption in this demographic and reduces the incidence of kidney stones.

Bone Resorptive Diseases

TRPV6 KO mice exhibit osteoporosis-like symptoms such as reduced bone mineral density and hypercalciuria. The hormone estrogen, the deficiency of which is linked to post-menopausal osteoporosis, also regulates the expression of TRPV6 in humans. Indeed, a lower calcium absorption seen in older postmenopausal women is attributed to reduced TRPV6.^[76] The C-terminal portion of Soricidin is a drug that inhibits Ca²⁺-uptake activity by binding to TRPV6. Preclinical studies of this drug have shown great promise in the treatment of bone resorptive diseases.

The high degree of similarity between Hereditary Vitamin D–Resistant Rickets (HVDRR) disease symptoms and observed phenotypes in TRPV6 KO mice has led some experts to postulate pathological connections between the disease and TRPV6 dysfunction. TRPV6 plays an important chondroprotective role by regulating multiple aspects of chondrocyte function, such as extracellular matrix secretion, the release of matrix-degrading enzymes, cell proliferation, and apoptosis.^[77] Furthermore, TRPV6 knockout mice display multiple osteoarthritis (OA) phenotypes such as cartilage fibrillation, eburnation, and loss of proteoglycans.

Pendred Syndrome

The dysfunction gene Slc26a4 has been linked to Pendred syndrome – a genetic disorder that results in syndromic deafness in children.^{[78] [79]} The disease is caused by mutations in which compromise the function of the encoded protein pendrin - an anion Cl⁻/HCO3 ⁻ exchanger expressed in the inner ear. The loss of function in this gene is thought to reduce the pH value of mammalian endolymph and impair Ca²⁺ absorption via TRPV5 and TRPV6. This in turn could prevent the uptake of Ca²⁺ and impairs the luminal reduction in Ca²⁺ concentration within the endolymphatic system of the ear.

Cancer

The overexpression of TRPV6 has been validated in the colon, parathyroid, pancreatic, and thyroid cancer whereas its expression is reportedly downregulated in esophageal cancer,^[80] non-small cell lung cancer,^[81] and renal cancer.^[82] TRPV6 is considered to be an oncochannel that is hypothesized to mediate cancer progression by triggering Ca²⁺-entry induced aberrations in molecular drivers regulating processes such as cell cycle, apoptosis, and migration; thereby conferring proliferative and survival advantages to cancer cells.^[83] Overexpression of TRPV6 correlates strongly with pathological stage, tumor grade, extra-prostatic invasion, lymph node metastasis, and resistance to androgen-targeted therapies in prostate cancer.^[84] The expression TRPV6 has been touted as a prognostic marker for advanced prostate cancer since its expression is strongly dependent on the grade of the tumor. Expression of TRPV6 is significantly elevated in breast adenocarcinoma tissue in comparison to normal breast tissue.^{[85] [86]} TRPV6 expression has been reported multiple breast cancer cell lines and prostate cancer cell lines.^{[87] [88] [89]} The prostate cancer cell lines PC-3 and LnCAP overexpress TRPV6 relative to benign epithelial cells PrEC and BPH-1. The silencing of TRPV6 in prostate cancer cells decreases proliferation rate, S-phase accumulation, and expression of tumor marker proliferating cell nuclear antigen (PCNA) expression. TRPV6 overexpression is believed to induce aberrant Ca^2+-uptake in prostate cancer line and activate transcription factor Nuclear Factor of Activated T cells (NFAT).

Expression of TRPV6 is upregulated by estrogen, progesterone, and estradiol in breast cancer cell line T47D. In agreement with these observations, the estrogen receptor antagonist Tamoxifen reduces TRPV6 expression in T47D cells and suppresses Ca²⁺-uptake of the channel in both ER-positive and ER-negative breast cancer cell lines.^[90] The overexpression of TRPV6 is associated with early-stage colon cancer and its silencing in colon cancer induces apoptosis and inhibits cancer cell proliferation.^[91] In terms of mechanism, mutations within the calmodulin-binding domains of TRPV6 channels confers invasive properties to colon adenocarcinoma cells.^[92] The proteins p38α and GADD45α are believed to upregulate TRPV6 expression signaling in SW480 colon cancer cells by enhancing vitamin D signaling.^[93] TRPV6 has been reported to amplify Insulin-like growth factors (IGF)-induced PI3K-PDK1-Akt signaling in human colon cancer and promote colon cancer.^[94]

TRPV6 is up-regulated in primary cancer tissues from pancreatic cancer patients and promotes the proliferation of pancreatic neuroendocrine tumors NFAT-dependent mechanisms.^[95] Silencing of TRPV6 induces apoptosis and cell cycle arrest in pancreatic cancer cells and inhibits their invasion, proliferation, and migration.^[96] Forced expression of TRPV6 in gastric cancer cells increases their sensitivity to capsaicin-induced apoptosis whereas the siRNA-mediated silencing of the channel suppresses this sensitivity.^[97] TRPV6 downregulation in esophageal carcinoma has been suggested to be a prognostic marker of disease-specific survival in patients suffering from esophageal cancer.^[98] Low TRPV5 and TRPV6 co-expression have suggested as predictive markers for poor recurrence-free survival in non-small cell lung cancer.

Pharmacological Targeting

Several chemical inhibitors are known to inhibit TRPV6. Some compounds that have demonstrated inhibitory activity towards TRPV6 include TH-1177, 2-Aminoethoxydiphenyl borate (2-APB), 2-APB derivative 22b, Econazole, Miconazole, Piperazine derivative Cis-22a, Capsaicin, Δ⁹-tetrahydrocannabivarin, Xestospongin C, Lidocaine, gold-caged nanoparticle (PTX-PP@Au NPs) and Sorcidin C-13 (SOR-C13) synthetic peptide. Among different inhibition strategies tested so far, the 13-amino acid peptide SOR-C13 has shown the most promise. This 13-amino acid peptide derived from 54-amino acid peptide found in the paralytic venom of the northern short-tailed shrew (Blarina brevicauda) reduces cancer growth in cell and animal models. This anti-cancer agent has recently completed a Phase I clinical safety trial that had enrolled 23 patients with advanced solid tumors of epithelial origin non-responsive to all standard-of-care treatments.

Regulation

The regulation of TRPV6 can be examined mainly in the context of its physiological, hormonal, and molecular factors. The hormonal regulation of TRPV6 has been characterized most extensively. In this regard, its regulation by the hormone vitamin D₃ and sex hormones has been examined in considerable detail. Rodent studies suggest that the TRPV6 channel is regulated by a wide range of physiological factors such as diet, age, gender, pregnancy, lactation, sex hormones, exercise, age, and gender. Some biological and pharmacological agents known to regulate TRPV6 include glucocorticoids, immunosuppressive drugs, and diuretics.

Vitamin D

Multiple dose-response and time-course experiments in rodents and colon cancer cell lines have conclusively shown TRPV6 mRNA is robustly induced by this vitamin D at extremely low concentrations.^{[99] [100]} At least five vitamin D response elements (VDREs) at positions −1.2, −2.1, −3.5, −4.3, and −5.5 kb relative to transcriptional start site (TSS) have been identified on TRPV6 transcripts.^[101] Among these five sites, VDREs at positions −1.2, −2.1, and −4.3 kb are significantly more responsive to 1,25-(OH)₂D₃ in comparison to VDREs located at −3.5 and −5.5 kb which do not appear to contribute substantially to vitamin D mediated transcriptional regulation in the intestine. Mechanism wise, TRPV6 transcription is initiated in response to vitamin D Receptor (VDR)-mediated signaling, although other non-direct mechanisms cannot be ruled out.^[102] Important steps in vitamin D mediated transcriptional regulation include 1) binding of vitamin D on its cognate vitamin D receptor (VDR), 2) the translocation of vitamin D receptor (VDR)-retinoid X receptor heterodimer complex in the nucleus, 3) binding VDR-RXR complex on the TRPV6 gene promoter, 4) recruitment of steroid receptor coactivator 1 and RNA polymerase II on the promoter, and 5) transcriptional activation mediated through histone H4 acetylation events.^[103]

Diet

The level of Ca²⁺ and vitamin D in the diet are the most important regulators of TRPV6 expression. The expression of TRPV6 is thought to be modulated strongly to fine-tune Ca²⁺ absorption from the diet, especially under conditions when dietary Ca²⁺ availability is low. In rodents, restricting Ca²⁺ availability in the diet induces dramatic up-regulation in the duodenal expression of TRPV6. Calcium influx from the diet and its subsequent binding to calbindin-D_9k could be the rate-limiting step that modulates vitamin D-dependent regulation TRPV6.^[104] When dietary Ca²⁺ is insufficient, normal blood calcium levels in TRPV6 KO mice are maintained at the expense of bone. In many rodent lines, genetic variations in TRPV6, calbindin-D_9k, PMCA1b mRNA influence intestinal Ca absorption and its impact on bone marrow density.^[105]

Pregnancy and lactation

Duodenal expression of TRPV6 transcripts is upregulated in WT and VDR KO mice during pregnancy and lactation.^[106] The hormone prolactin upregulates TRPV6 transcription and facilitates an increase in intestinal Ca²⁺ absorption in lactating and pregnant rats, possibly as an adaptive mechanism for overcoming the loss in bone mineralization content during lactation.^[107]

Aging

The intestinal expression of TRPV6 in mice varies dramatically by age and relative tissue location.^[108] The duodenal expression of TRPV6 is undetectable at P1 and increases 6-fold as mice age to P14. Similarly, the expression also varies with age in the jejunum, where TRPV6 levels increases from P1 to P14, become weak at 1-month age and becomes undetectable in older mice. The expression of TRPV6 in older rats (12-months) is at least 50% lower in comparison to younger counterparts (2-months old). In both WT and VDR KO mice, the age-associated decline in intestinal absorption of Ca²⁺ is accompanied by a decline in duodenal expression of TRPV6.^[109]

Sex hormones

Sex hormones play an important role in the regulation of TRPV6. In comparison to male mice, female mice exhibit a 2-fold higher increase in duodenal expression of TRPV6 mRNA following vitamin D treatment. Sex hormone-associated differential regulation of TRPV6 across genders is believed to be correlated to differences in relative risk to osteoporosis in older postmenopausal women which have been reported to have lower TRPV6 and VDR expression in comparison to males.

Estrogen treatment upregulates TRPV6 transcripts by 8-fold in VDR KO mice and by 4-fold in ovariectomized mice. Greater than 50% reduction in TRPV6 mRNA has been observed in estrogen receptor α KO mice.^[106] It is believed that estrogen could be differentially regulating Ca²⁺ absorption in the duodenum by increasing TRPV6 expression through ERα.^[110] Anti-progesterone agent RU486 and anti-estrogen agent ICI 182,780 suppress TRPV6 expression in rodents by their respective antagonist action on progesterone and estrogen receptors.^[111] Estrogen, progesterone, and dexamethasone are known to upregulate TRPV6 expression in the cerebral cortex and hypothalamus of mice suggesting a potential involvement of TRPV6 in calcium absorption in the brain.^[112]

Glucocorticoids

Subcutaneous administration of glucocorticoids dexamethasone induces both renal and intestinal expression of TRPV6 in mice within 24 hours of whereas oral application of prednisolone reduction in TRPV6 which is also accompanied by reduced Ca²⁺ absorption in duodenum.^{[113] [114]} Intestinal regulation of TRPV6 in response to glucocorticoids appears to be VDR-dependent. The enzyme serum and glucocorticoid-regulated kinase 1 (SKG1) regulates TRPV6 expression by enhancing phosphatidylinositol-3-phosphate-5-kinase PIKfyve (PIP5K3).^[115] This kinase is critical for the generation of secondary messenger PIP₂, a known lipid activator of TRPV6. ----

• TRPV
• TRPV5
• calcium channels
• calcium absorption
• transcellular pathway
• gating mechanism
• calmodulin
• maternal-fetal transport
• transient neonatal hyperparathyroidism
• chronic pancreatitis
• kidney stones
• cancer

Further reading

• Heiner I, Eisfeld J, Lückhoff A . Role and regulation of TRP channels in neutrophil granulocytes . Cell Calcium . 33 . 5–6 . 533–40 . 2004 . 12765698 . 10.1016/S0143-4160(03)00058-7 .
• Clapham DE, Julius D, Montell C, Schultz G . International Union of Pharmacology. XLIX. Nomenclature and structure-function relationships of transient receptor potential channels . Pharmacological Reviews . 57 . 4 . 427–50 . December 2005 . 16382100 . 10.1124/pr.57.4.6 . 17936350 .
• Book: Wissenbach U, Niemeyer BA . Transient Receptor Potential (TRP) Channels . TRPV6 . 179 . 179 . 221–34 . 2007 . 17217060 . 10.1007/978-3-540-34891-7_13 . 978-3-540-34889-4 . Handbook of Experimental Pharmacology .
• Schoeber JP, Hoenderop JG, Bindels RJ . Concerted action of associated proteins in the regulation of TRPV5 and TRPV6 . Biochemical Society Transactions . 35 . Pt 1 . 115–9 . February 2007 . 17233615 . 10.1042/BST0350115 .

Notes and References

1. Venkatachalam K, Montell C . TRP channels . Annual Review of Biochemistry . 76 . 387–417 . 2007 . 17579562 . 4196875 . 10.1146/annurev.biochem.75.103004.142819 .
2. Montell C, Birnbaumer L, Flockerzi V, Bindels RJ, Bruford EA, Caterina MJ, Clapham DE, Harteneck C, Heller S, Julius D, Kojima I, Mori Y, Penner R, Prawitt D, Scharenberg AM, Schultz G, Shimizu N, Zhu MX . 6 . A unified nomenclature for the superfamily of TRP cation channels . Molecular Cell . 9 . 2 . 229–31 . February 2002 . 11864597 . 10.1016/s1097-2765(02)00448-3 . 1106536919 . free .
3. Yue L, Peng JB, Hediger MA, Clapham DE . CaT1 manifests the pore properties of the calcium-release-activated calcium channel . Nature . 410 . 6829 . 705–9 . April 2001 . 11287959 . 10.1038/35070596 . 4404582 . 2001Natur.410..705Y .
4. Yelshanskaya MV, Nadezhdin KD, Kurnikova MG, Sobolevsky AI . Structure and function of the calcium-selective TRP channel TRPV6 . The Journal of Physiology . February 2020 . 599 . 10 . 2673–2697 . 32073143 . 10.1113/JP279024 . 7689878 . free .
5. Book: Peng JB, Suzuki Y, Gyimesi G, Hediger MA . TRPV5 and TRPV6 Calcium-Selective Channels. . Calcium Entry Channels in Non-Excitable Cells . 2018 . 10.1201/9781315152592-13 . 241–274 . Boca Raton, FL . Methods in signal transduction series . CRC Press/Taylor & Francis . 30299660 . 978-1-315-15259-2 .
6. Peng JB, Chen XZ, Berger UV, Vassilev PM, Tsukaguchi H, Brown EM, Hediger MA . Molecular cloning and characterization of a channel-like transporter mediating intestinal calcium absorption . The Journal of Biological Chemistry . 274 . 32 . 22739–46 . August 1999 . 10428857 . 10.1074/jbc.274.32.22739 . 23616713 . free .
7. Peng JB, Chen XZ, Berger UV, Weremowicz S, Morton CC, Vassilev PM, Brown EM, Hediger MA . 6 . Human calcium transport protein CaT1 . Biochemical and Biophysical Research Communications . 278 . 2 . 326–32 . November 2000 . 11097838 . 10.1006/bbrc.2000.3716 .
8. Weber K, Erben RG, Rump A, Adamski J . Gene structure and regulation of the murine epithelial calcium channels ECaC1 and 2 . Biochemical and Biophysical Research Communications . 289 . 5 . 1287–94 . December 2001 . 11741335 . 10.1006/bbrc.2001.6121 .
9. Hoenderop JG, Vennekens R, Müller D, Prenen J, Droogmans G, Bindels RJ, Nilius B . Function and expression of the epithelial Ca(2+) channel family: comparison of mammalian ECaC1 and 2 . The Journal of Physiology . 537 . Pt 3 . 747–61 . December 2001 . 11744752 . 2278984 . 10.1113/jphysiol.2001.012917 .
10. Wissenbach U, Niemeyer BA, Fixemer T, Schneidewind A, Trost C, Cavalie A, Reus K, Meese E, Bonkhoff H, Flockerzi V . 6 . Expression of CaT-like, a novel calcium-selective channel, correlates with the malignancy of prostate cancer . The Journal of Biological Chemistry . 276 . 22 . 19461–8 . June 2001 . 11278579 . 10.1074/jbc.m009895200 . 25833991 . free .
11. Clapham DE, Julius D, Montell C, Schultz G . International Union of Pharmacology. XLIX. Nomenclature and structure-function relationships of transient receptor potential channels . Pharmacological Reviews . 57 . 4 . 427–50 . December 2005 . 16382100 . 10.1124/pr.57.4.6 . 17936350 .
12. Müller D, Hoenderop JG, Merkx GF, van Os CH, Bindels RJ . Gene structure and chromosomal mapping of human epithelial calcium channel . Biochemical and Biophysical Research Communications . 275 . 1 . 47–52 . August 2000 . 10944439 . 10.1006/bbrc.2000.3227 .
13. Book: Fecher-Trost C, Weissgerber P, Wissenbach U . TRPV6 Channels . Mammalian Transient Receptor Potential (TRP) Cation Channels . Handbook of Experimental Pharmacology . 222 . 359–84 . 2014 . 24756713 . 10.1007/978-3-642-54215-2_14 . Springer Berlin Heidelberg . 978-3-642-54214-5 . Berlin, Heidelberg .
14. Fecher-Trost C, Wissenbach U, Beck A, Schalkowsky P, Stoerger C, Doerr J, Dembek A, Simon-Thomas M, Weber A, Wollenberg P, Ruppert T, Middendorff R, Maurer HH, Flockerzi V . 6 . The in vivo TRPV6 protein starts at a non-AUG triplet, decoded as methionine, upstream of canonical initiation at AUG . The Journal of Biological Chemistry . 288 . 23 . 16629–44 . June 2013 . 23612980 . 3675598 . 10.1074/jbc.M113.469726 . free .
15. Flores-Aldama L, Vandewege MW, Zavala K, Colenso CK, Gonzalez W, Brauchi SE, Opazo JC . Evolutionary analyses reveal independent origins of gene repertoires and structural motifs associated to fast inactivation in calcium-selective TRPV channels . Scientific Reports . 10 . 1 . 8684 . May 2020 . 32457384 . 7250927 . 10.1038/s41598-020-65679-6 . 2020NatSR..10.8684F .
16. Akey JM, Swanson WJ, Madeoy J, Eberle M, Shriver MD . TRPV6 exhibits unusual patterns of polymorphism and divergence in worldwide populations . Human Molecular Genetics . 15 . 13 . 2106–13 . July 2006 . 16717058 . 10.1093/hmg/ddl134 . free .
17. Soejima M, Tachida H, Koda Y . Sequence analysis of human TRPV6 suggests positive selection outside Africa . Biochemical Genetics . 47 . 1–2 . 147–53 . February 2009 . 19169858 . 10.1007/s10528-009-9222-x . 39897282 .
18. Book: Peng JB . Transient Receptor Potential Channels . TRPV5 and TRPV6 in Transcellular Ca2+ Transport: Regulation, Gene Duplication, and Polymorphisms in African Populations . Advances in Experimental Medicine and Biology . 704 . 239–75 . 2011 . 21290300 . 10.1007/978-94-007-0265-3_14 . 978-94-007-0264-6 .
19. Zhuang L, Peng JB, Tou L, Takanaga H, Adam RM, Hediger MA, Freeman MR . Calcium-selective ion channel, CaT1, is apically localized in gastrointestinal tract epithelia and is aberrantly expressed in human malignancies . Laboratory Investigation; A Journal of Technical Methods and Pathology . 82 . 12 . 1755–64 . December 2002 . 12480925 . 10.1097/01.lab.0000043910.41414.e7 . 6053178 . free .
20. Web site: TRPV6 protein expression summary . The Human Protein Atlas. 2020-08-01 .
21. Lehen'kyi V, Raphaël M, Prevarskaya N . The role of the TRPV6 channel in cancer . The Journal of Physiology . 590 . 6 . 1369–76 . March 2012 . 22331416 . 3382328 . 10.1113/jphysiol.2011.225862 .
22. Hirnet D, Olausson J, Fecher-Trost C, Bödding M, Nastainczyk W, Wissenbach U, Flockerzi V, Freichel M . 6 . The TRPV6 gene, cDNA and protein . Cell Calcium . 33 . 5–6 . 509–18 . May 2003 . 12765696 . 10.1016/s0143-4160(03)00066-6 .
23. Nijenhuis T, Hoenderop JG, van der Kemp AW, Bindels RJ . Localization and regulation of the epithelial Ca2+ channel TRPV6 in the kidney . Journal of the American Society of Nephrology . 14 . 11 . 2731–40 . November 2003 . 14569082 . 10.1097/01.asn.0000094081.78893.e8 . free .
24. Stewart JM . TRPV6 as A Target for Cancer Therapy . Journal of Cancer . 11 . 2 . 374–387 . 2020 . 31897233 . 6930427 . 10.7150/jca.31640 .
25. Chen F, Ni B, Yang YO, Ye T, Chen A . Knockout of TRPV6 causes osteopenia in mice by increasing osteoclastic differentiation and activity . Cellular Physiology and Biochemistry . 33 . 3 . 796–809 . 2014 . 24686448 . 10.1159/000358653 . 19539099 . free .
26. van der Eerden BC, Weissgerber P, Fratzl-Zelman N, Olausson J, Hoenderop JG, Schreuders-Koedam M, Eijken M, Roschger P, de Vries TJ, Chiba H, Klaushofer K, Flockerzi V, Bindels RJ, Freichel M, van Leeuwen JP . 6 . The transient receptor potential channel TRPV6 is dynamically expressed in bone cells but is not crucial for bone mineralization in mice . Journal of Cellular Physiology . 227 . 5 . 1951–9 . May 2012 . 21732366 . 10.1002/jcp.22923 . 7094759 .
27. Little R, Muimo R, Robson L, Harris K, Grabowski PS . The transient receptor potential ion channel TRPV6 is expressed at low levels in osteoblasts and has little role in osteoblast calcium uptake . PLOS ONE . 6 . 11 . e28166 . 2011-11-29 . 22163264 . 3226639 . 10.1371/journal.pone.0028166 . 2011PLoSO...628166L . free .
28. Saotome K, Singh AK, Yelshanskaya MV, Sobolevsky AI . Crystal structure of the epithelial calcium channel TRPV6 . Nature . 534 . 7608 . 506–11 . June 2016 . 27296226 . 4919205 . 10.1038/nature17975 . 2016Natur.534..506S .
29. Singh AK, Saotome K, Sobolevsky AI . Swapping of transmembrane domains in the epithelial calcium channel TRPV6 . Scientific Reports . 7 . 1 . 10669 . September 2017 . 28878326 . 5587609 . 10.1038/s41598-017-10993-9 . 2017NatSR...710669S .
30. Lu P, Boros S, Chang Q, Bindels RJ, Hoenderop JG . The beta-glucuronidase klotho exclusively activates the epithelial Ca2+ channels TRPV5 and TRPV6 . Nephrology, Dialysis, Transplantation . 23 . 11 . 3397–402 . November 2008 . 18495742 . 10.1093/ndt/gfn291 . free . 2066/70822 . free .
31. Owsianik G, Talavera K, Voets T, Nilius B . Permeation and selectivity of TRP channels . Annual Review of Physiology . 68 . 1 . 685–717 . January 2006 . 16460288 . 10.1146/annurev.physiol.68.040204.101406 .
32. Voets T, Janssens A, Droogmans G, Nilius B . Outer pore architecture of a Ca2+-selective TRP channel . The Journal of Biological Chemistry . 279 . 15 . 15223–30 . April 2004 . 14736889 . 10.1074/jbc.m312076200 . 23827272 . free .
33. Voets T, Janssens A, Prenen J, Droogmans G, Nilius B . Mg2+-dependent gating and strong inward rectification of the cation channel TRPV6 . The Journal of General Physiology . 121 . 3 . 245–60 . March 2003 . 12601087 . 2217333 . 10.1085/jgp.20028752 .
34. Kovacs G, Danko T, Bergeron MJ, Balazs B, Suzuki Y, Zsembery A, Hediger MA . Heavy metal cations permeate the TRPV6 epithelial cation channel . Cell Calcium . 49 . 1 . 43–55 . January 2011 . 21146870 . 10.1016/j.ceca.2010.11.007 . 41086787 .
35. Singh AK, Saotome K, Sobolevsky AI . Swapping of transmembrane domains in the epithelial calcium channel TRPV6 . Scientific Reports . 7 . 1 . 10669 . September 2017 . 28878326 . 5587609 . 10.1038/s41598-017-10993-9 . 2017NatSR...710669S . 10.1101/141523 .
36. Cao C, Zakharian E, Borbiro I, Rohacs T . Interplay between calmodulin and phosphatidylinositol 4,5-bisphosphate in Ca2+-induced inactivation of transient receptor potential vanilloid 6 channels . The Journal of Biological Chemistry . 288 . 8 . 5278–90 . February 2013 . 23300090 . 3581402 . 10.1074/jbc.M112.409482 . free .
37. Bödding M, Flockerzi V . Ca2+ dependence of the Ca2+-selective TRPV6 channel . The Journal of Biological Chemistry . 279 . 35 . 36546–52 . August 2004 . 15184369 . 10.1074/jbc.m404679200 . 22842694 . free .
38. Lambers TT, Weidema AF, Nilius B, Hoenderop JG, Bindels RJ . Regulation of the mouse epithelial Ca2(+) channel TRPV6 by the Ca(2+)-sensor calmodulin . The Journal of Biological Chemistry . 279 . 28 . 28855–61 . July 2004 . 15123711 . 10.1074/jbc.m313637200 . 23453339 . free . 2066/57723 . free .
39. Zakharian E, Cao C, Rohacs T . Intracellular ATP supports TRPV6 activity via lipid kinases and the generation of PtdIns(4,5) P₂ . FASEB Journal . 25 . 11 . 3915–28 . November 2011 . 21810903 . 3205842 . 10.1096/fj.11-184630 . free .
40. Thyagarajan B, Benn BS, Christakos S, Rohacs T . Phospholipase C-mediated regulation of transient receptor potential vanilloid 6 channels: implications in active intestinal Ca2+ transport . Molecular Pharmacology . 75 . 3 . 608–16 . March 2009 . 19073818 . 2684912 . 10.1124/mol.108.052449 .
41. Derler I, Hofbauer M, Kahr H, Fritsch R, Muik M, Kepplinger K, Hack ME, Moritz S, Schindl R, Groschner K, Romanin C . 6 . Dynamic but not constitutive association of calmodulin with rat TRPV6 channels enables fine tuning of Ca2+-dependent inactivation . The Journal of Physiology . 577 . Pt 1 . 31–44 . November 2006 . 16959851 . 2000671 . 10.1113/jphysiol.2006.118661 .
42. Niemeyer BA, Bergs C, Wissenbach U, Flockerzi V, Trost C . Competitive regulation of CaT-like-mediated Ca2+ entry by protein kinase C and calmodulin . Proceedings of the National Academy of Sciences of the United States of America . 98 . 6 . 3600–5 . March 2001 . 11248124 . 30699 . 10.1073/pnas.051511398 . 2001PNAS...98.3600N . free .
43. Shin YC, Shin SY, So I, Kwon D, Jeon JH . TRIP Database: a manually curated database of protein-protein interactions for mammalian TRP channels . Nucleic Acids Research . 39 . Database issue . D356-61 . January 2011 . 20851834 . 10.1093/nar/gkq814 . 3013757 . 16278877 . free .
44. Suzuki Y, Landowski CP, Hediger MA . Mechanisms and regulation of epithelial Ca2+ absorption in health and disease . Annual Review of Physiology . 70 . 1 . 257–71 . March 2008 . 17850211 . 10.1146/annurev.physiol.69.031905.161003 .
45. Suzuki Y, Kovacs CS, Takanaga H, Peng JB, Landowski CP, Hediger MA . Calcium channel TRPV6 is involved in murine maternal-fetal calcium transport . Journal of Bone and Mineral Research . 23 . 8 . 1249–56 . August 2008 . 18348695 . 2680174 . 10.1359/jbmr.080314 .
46. Lehen'kyi V, Beck B, Polakowska R, Charveron M, Bordat P, Skryma R, Prevarskaya N . TRPV6 is a Ca2+ entry channel essential for Ca2+-induced differentiation of human keratinocytes . The Journal of Biological Chemistry . 282 . 31 . 22582–91 . August 2007 . 17550901 . 10.1074/jbc.m611398200 . 22082147 . free .
47. Yamauchi D, Nakaya K, Raveendran NN, Harbidge DG, Singh R, Wangemann P, Marcus DC . Expression of epithelial calcium transport system in rat cochlea and vestibular labyrinth . BMC Physiology . 10 . 1 . 1 . January 2010 . 20113508 . 10.1186/1472-6793-10-1 . 2825184 . 5773117 . free .
48. Yamauchi D, Raveendran NN, Pondugula SR, Kampalli SB, Sanneman JD, Harbidge DG, Marcus DC . Vitamin D upregulates expression of ECaC1 mRNA in semicircular canal . Biochemical and Biophysical Research Communications . 331 . 4 . 1353–7 . June 2005 . 15883024 . 10.1016/j.bbrc.2005.04.053 .
49. Weissgerber P, Kriebs U, Tsvilovskyy V, Olausson J, Kretz O, Stoerger C, Vennekens R, Wissenbach U, Middendorff R, Flockerzi V, Freichel M . 6 . Male fertility depends on Ca²+ absorption by TRPV6 in epididymal epithelia . Science Signaling . 4 . 171 . ra27 . May 2011 . 21540454 . 10.1126/scisignal.2001791 . 206670887 .
50. Weissgerber P, Kriebs U, Tsvilovskyy V, Olausson J, Kretz O, Stoerger C, Mannebach S, Wissenbach U, Vennekens R, Middendorff R, Flockerzi V, Freichel M . 6 . Excision of Trpv6 gene leads to severe defects in epididymal Ca2+ absorption and male fertility much like single D541A pore mutation . The Journal of Biological Chemistry . 287 . 22 . 17930–41 . May 2012 . 22427671 . 3365704 . 10.1074/jbc.m111.328286 . free .
51. Diaz de Barboza G, Guizzardi S, Tolosa de Talamoni N . Molecular aspects of intestinal calcium absorption . World Journal of Gastroenterology . 21 . 23 . 7142–54 . June 2015 . 26109800 . 4476875 . 10.3748/wjg.v21.i23.7142 . free .
52. Bianco SD, Peng JB, Takanaga H, Suzuki Y, Crescenzi A, Kos CH, Zhuang L, Freeman MR, Gouveia CH, Wu J, Luo H, Mauro T, Brown EM, Hediger MA . 6 . Marked disturbance of calcium homeostasis in mice with targeted disruption of the Trpv6 calcium channel gene . Journal of Bone and Mineral Research . 22 . 2 . 274–85 . February 2007 . 17129178 . 4548943 . 10.1359/jbmr.061110 .
53. Azarpeykan S, Dittmer KE, Marshall JC, Perera KC, Gee EK, Acke E, Thompson KG . Evaluation and Comparison of Vitamin D Responsive Gene Expression in Ovine, Canine and Equine Kidney . PLOS ONE . 11 . 9 . e0162598 . 2016-09-15 . 27632366 . 5025205 . 10.1371/journal.pone.0162598 . 2016PLoSO..1162598A . free .
54. Stulc J . Placental transfer of inorganic ions and water . Physiological Reviews . 77 . 3 . 805–36 . July 1997 . 9234966 . 10.1152/physrev.1997.77.3.805 .
55. Kovacs CS, Kronenberg HM . Maternal-fetal calcium and bone metabolism during pregnancy, puerperium, and lactation . Endocrine Reviews . 18 . 6 . 832–72 . December 1997 . 10.1210/edrv.18.6.0319 . 9408745 . free .
56. Sharma D, Shastri S, Sharma P . Intrauterine Growth Restriction: Antenatal and Postnatal Aspects . Clinical Medicine Insights. Pediatrics . 10 . 67–83 . January 2016 . 27441006 . 4946587 . 10.4137/cmped.s40070 .
57. Bernucci L, Henríquez M, Díaz P, Riquelme G . Diverse calcium channel types are present in the human placental syncytiotrophoblast basal membrane . Placenta . 27 . 11–12 . 1082–95 . November 2006 . 16564089 . 10.1016/j.placenta.2005.12.007 . 10533/178038 . free .
58. Lee GS, Jeung EB . Uterine TRPV6 expression during the estrous cycle and pregnancy in a mouse model . American Journal of Physiology. Endocrinology and Metabolism . 293 . 1 . E132-8 . July 2007 . 17374692 . 10.1152/ajpendo.00666.2006 .
59. Moreau R, Hamel A, Daoud G, Simoneau L, Lafond J . Expression of calcium channels along the differentiation of cultured trophoblast cells from human term placenta . Biology of Reproduction . 67 . 5 . 1473–9 . November 2002 . 12390878 . 10.1095/biolreprod.102.005397 . 23847059 . free .
60. Yang H, Kim TH, An BS, Choi KC, Lee HH, Kim JM, Jeung EB . Differential expression of calcium transport channels in placenta primary cells and tissues derived from preeclamptic placenta . Molecular and Cellular Endocrinology . 367 . 1–2 . 21–30 . March 2013 . 23267838 . 10.1016/j.mce.2012.12.012 . 5276054 .
61. Miura S, Sato K, Kato-Negishi M, Teshima T, Takeuchi S . Fluid shear triggers microvilli formation via mechanosensitive activation of TRPV6 . Nature Communications . 6 . 1 . 8871 . November 2015 . 26563429 . 4660203 . 10.1038/ncomms9871 . 2015NatCo...6.8871M .
62. Ecroyd H, Asquith KL, Jones RC, Aitken RJ . The development of signal transduction pathways during epididymal maturation is calcium dependent . Developmental Biology . 268 . 1 . 53–63 . April 2004 . 15031104 . 10.1016/j.ydbio.2003.12.015 . free .
63. Gao D, Zhang BL, Leung MC, Au SC, Wong PY, Shum WW . Coupling of TRPV6 and TMEM16A in epithelial principal cells of the rat epididymis . The Journal of General Physiology . 148 . 2 . 161–82 . August 2016 . 27481714 . 4969799 . 10.1085/jgp.201611626 .
64. Lieben L, Benn BS, Ajibade D, Stockmans I, Moermans K, Hediger MA, Peng JB, Christakos S, Bouillon R, Carmeliet G . 6 . Trpv6 mediates intestinal calcium absorption during calcium restriction and contributes to bone homeostasis . Bone . 47 . 2 . 301–8 . August 2010 . 20399919 . 2902603 . 10.1016/j.bone.2010.04.595 .
65. Lieben L, Carmeliet G . The Involvement of TRP Channels in Bone Homeostasis . Frontiers in Endocrinology . 3 . 99 . 2012 . 22934090 . 3422722 . 10.3389/fendo.2012.00099 . free .
66. Tu CL, Bikle DD . Role of the calcium-sensing receptor in calcium regulation of epidermal differentiation and function . Best Practice & Research. Clinical Endocrinology & Metabolism . 27 . 3 . 415–27 . June 2013 . 23856269 . 3713412 . 10.1016/j.beem.2013.03.002 .
67. De Clercq K, Held K, Van Bree R, Meuleman C, Peeraer K, Tomassetti C, Voets T, D'Hooghe T, Vriens J . 6 . Functional expression of transient receptor potential channels in human endometrial stromal cells during the luteal phase of the menstrual cycle . Human Reproduction . 30 . 6 . 1421–36 . June 2015 . 25820697 . 10.1093/humrep/dev068 . free .
68. Yang H, Choi KC, Hyun SH, Jeung EB . Coexpression and estrogen-mediated regulation of TRPV6 and PMCA1 in the human endometrium during the menstrual cycle . Molecular Reproduction and Development . 78 . 4 . 274–82 . April 2011 . 21400627 . 10.1002/mrd.21303 . 21140465 .
69. De Clercq K, Van den Eynde C, Hennes A, Van Bree R, Voets T, Vriens J . The functional expression of transient receptor potential channels in the mouse endometrium . Human Reproduction . 32 . 3 . 615–630 . March 2017 . 28077439 . 10.1093/humrep/dew344 . 3409475 . free .
70. Suzuki Y, Chitayat D, Sawada H, Deardorff MA, McLaughlin HM, Begtrup A, Millar K, Harrington J, Chong K, Roifman M, Grand K, Tominaga M, Takada F, Shuster S, Obara M, Mutoh H, Kushima R, Nishimura G . TRPV6 Variants Interfere with Maternal-Fetal Calcium Transport through the Placenta and Cause Transient Neonatal Hyperparathyroidism . American Journal of Human Genetics . 102 . 6 . 1104–1114 . June 2018 . 29861107 . 5992228 . 10.1016/j.ajhg.2018.04.006 .
71. Yamashita S, Mizumoto H, Sawada H, Suzuki Y, Hata D . TRPV6 Gene Mutation in a Dizygous Twin With Transient Neonatal Hyperparathyroidism . Journal of the Endocrine Society . 3 . 3 . 602–606 . March 2019 . 30820485 . 6389352 . 10.1210/js.2018-00374 .
72. Burren CP, Caswell R, Castle B, Welch CR, Hilliard TN, Smithson SF, Ellard S . TRPV6 compound heterozygous variants result in impaired placental calcium transport and severe undermineralization and dysplasia of the fetal skeleton . American Journal of Medical Genetics. Part A . 176 . 9 . 1950–1955 . September 2018 . 30144375 . 6563443 . 10.1002/ajmg.a.40484 .
73. Zou WB, Wang YC, Ren XL, Wang L, Deng SJ, Mao XT, Li ZS, Liao Z . 6 . TRPV6 variants confer susceptibility to chronic pancreatitis in the Chinese population . Human Mutation . 41 . 8 . 1351–1357 . August 2020 . 32383311 . 10.1002/humu.24032 . free .
74. Masamune A, Kotani H, Sörgel FL, Chen JM, Hamada S, Sakaguchi R, Masson E, Nakano E, Kakuta Y, Niihori T, Funayama R, Shirota M, Hirano T, Kawamoto T, Hosokoshi A, Kume K, Unger L, Ewers M, Laumen H, Bugert P, Mori MX, Tsvilovskyy V, Weißgerber P, Kriebs U, Fecher-Trost C, Freichel M, Diakopoulos KN, Berninger A, Lesina M, Ishii K, Itoi T, Ikeura T, Okazaki K, Kaune T, Rosendahl J, Nagasaki M, Uezono Y, Algül H, Nakayama K, Matsubara Y, Aoki Y, Férec C, Mori Y, Witt H, Shimosegawa T . 6 . Variants That Affect Function of Calcium Channel TRPV6 Are Associated With Early-Onset Chronic Pancreatitis . Gastroenterology . 158 . 6 . 1626–1641.e8 . May 2020 . 31930989 . 10.1053/j.gastro.2020.01.005 . free .
75. Book: Suzuki, Yoshiro Pasch, Andreas Bonny, Olivier Mohaupt, Markus G. Hediger, Matthias A. Frey, Felix J.. Gain-of-function haplotype in the epithelial calcium channel TRPV6 is a risk factor for renal calcium stone formation. Human Molecular Genetics. 2017-08-02. 17. 11. 1613–8. 10.1093/hmg/ddn048. 18276610. 1156692319.
76. Walters JR, Balesaria S, Chavele KM, Taylor V, Berry JL, Khair U, Barley NF, van Heel DA, Field J, Hayat JO, Bhattacharjee A, Jeffery R, Poulsom R . 6 . Calcium channel TRPV6 expression in human duodenum: different relationships to the vitamin D system and aging in men and women . Journal of Bone and Mineral Research . 21 . 11 . 1770–7 . November 2006 . 17002582 . 10.1359/jbmr.060721 . 22847166 . free .
77. Sherwood J, Bertrand J, Seidemann M, Dell'Accio F, Pap T . April 2016. Activation of the transient receptor potential cation channel TRPC6 is required for chondrocyte phenotypic stability. Osteoarthritis and Cartilage. 24. S152–S153. 10.1016/j.joca.2016.01.298. 1063-4584. free.
78. Nakaya K, Harbidge DG, Wangemann P, Schultz BD, Green ED, Wall SM, Marcus DC . Lack of pendrin HCO3- transport elevates vestibular endolymphatic [Ca2+] by inhibition of acid-sensitive TRPV5 and TRPV6 channels . American Journal of Physiology. Renal Physiology . 292 . 5 . F1314-21 . May 2007 . 17200157 . 2515270 . 10.1152/ajprenal.00432.2006 .
79. Dror AA, Brownstein Z, Avraham KB . Integration of human and mouse genetics reveals pendrin function in hearing and deafness . Cellular Physiology and Biochemistry . 28 . 3 . 535–44 . 2011 . 22116368 . 3709173 . 10.1159/000335163 .
80. Sun F, Xiao L, Jang XX, Xiong Y, Li Q, Yue XJ, Wei YJ, Wei YX, Ma YL, Yu YH . 6 . TRPV6 is a prognostic marker in early-stage cervical squamous cell carcinoma . Tumour Biology . 37 . 12 . October 2016 . 15743–15751 . 27747588 . 10.1007/s13277-016-5368-4 . 6445506 .
81. Fan H, Shen YX, Yuan YF . Expression and prognostic roles of TRPV5 and TRPV6 in non-small cell lung cancer after curative resection . Asian Pacific Journal of Cancer Prevention . 15 . 6 . 2559–63 . 2014-03-30 . 24761864 . 10.7314/apjcp.2014.15.6.2559 . free .
82. Wu Y, Miyamoto T, Li K, Nakagomi H, Sawada N, Kira S, Kobayashi H, Zakohji H, Tsuchida T, Fukazawa M, Araki I, Takeda M . 6 . Decreased expression of the epithelial Ca2+ channel TRPV5 and TRPV6 in human renal cell carcinoma associated with vitamin D receptor . The Journal of Urology . 186 . 6 . 2419–25 . December 2011 . 22019165 . 10.1016/j.juro.2011.07.086 .
83. Peng JB, Zhuang L, Berger UV, Adam RM, Williams BJ, Brown EM, Hediger MA, Freeman MR . 6 . CaT1 expression correlates with tumor grade in prostate cancer . Biochemical and Biophysical Research Communications . 282 . 3 . 729–34 . April 2001 . 11401523 . 10.1006/bbrc.2001.4638 .
84. Fixemer T, Wissenbach U, Flockerzi V, Bonkhoff H . Expression of the Ca2+-selective cation channel TRPV6 in human prostate cancer: a novel prognostic marker for tumor progression . Oncogene . 22 . 49 . 7858–61 . October 2003 . 14586412 . 10.1038/sj.onc.1206895 . 23626142 . free .
85. Dhennin-Duthille I, Gautier M, Faouzi M, Guilbert A, Brevet M, Vaudry D, Ahidouch A, Sevestre H, Ouadid-Ahidouch H . 6 . High expression of transient receptor potential channels in human breast cancer epithelial cells and tissues: correlation with pathological parameters . Cellular Physiology and Biochemistry . 28 . 5 . 813–22 . 2011 . 22178934 . 10.1159/000335795 . 45740662 . free .
86. Bolanz KA, Hediger MA, Landowski CP . The role of TRPV6 in breast carcinogenesis . Molecular Cancer Therapeutics . 7 . 2 . 271–9 . February 2008 . 18245667 . 10.1158/1535-7163.mct-07-0478 . 17158946 . free .
87. Peters AA, Simpson PT, Bassett JJ, Lee JM, Da Silva L, Reid LE, Song S, Parat MO, Lakhani SR, Kenny PA, Roberts-Thomson SJ, Monteith GR . 6 . Calcium channel TRPV6 as a potential therapeutic target in estrogen receptor-negative breast cancer . Molecular Cancer Therapeutics . 11 . 10 . 2158–68 . October 2012 . 22807578 . 10.1158/1535-7163.mct-11-0965 . 207614323 . free .
88. Lehen'kyi V, Flourakis M, Skryma R, Prevarskaya N . TRPV6 channel controls prostate cancer cell proliferation via Ca(2+)/NFAT-dependent pathways . Oncogene . 26 . 52 . 7380–5 . November 2007 . 17533368 . 10.1038/sj.onc.1210545 . 482760 . free .
89. Lehen'kyi V, Raphaël M, Oulidi A, Flourakis M, Khalimonchyk S, Kondratskyi A, Gordienko DV, Mauroy B, Bonnal JL, Skryma R, Prevarskaya N . 6 . TRPV6 determines the effect of vitamin D3 on prostate cancer cell growth . PLOS ONE . 6 . 2 . e16856 . February 2011 . 21347289 . 3037935 . 10.1371/journal.pone.0016856 . 2011PLoSO...616856L . free .
90. Bolanz KA, Kovacs GG, Landowski CP, Hediger MA . Tamoxifen inhibits TRPV6 activity via estrogen receptor-independent pathways in TRPV6-expressing MCF-7 breast cancer cells . Molecular Cancer Research . 7 . 12 . 2000–10 . December 2009 . 19996302 . 10.1158/1541-7786.mcr-09-0188 . 26337876 . free .
91. Peleg S, Sellin JH, Wang Y, Freeman MR, Umar S . Suppression of aberrant transient receptor potential cation channel, subfamily V, member 6 expression in hyperproliferative colonic crypts by dietary calcium . American Journal of Physiology. Gastrointestinal and Liver Physiology . 299 . 3 . G593-601 . September 2010 . 20508153 . 2950683 . 10.1152/ajpgi.00193.2010 .
92. Arbabian A, Iftinca M, Altier C, Singh PP, Isambert H, Coscoy S . Mutations in calmodulin-binding domains of TRPV4/6 channels confer invasive properties to colon adenocarcinoma cells . Channels . 14 . 1 . 101–109 . December 2020 . 32186440 . 7153789 . 10.1080/19336950.2020.1740506 .
93. Ishizawa M, Akagi D, Yamamoto J, Makishima M . 3 enhances TRPV6 transcription through p38 MAPK activation and GADD45 expression . The Journal of Steroid Biochemistry and Molecular Biology . 172 . 55–61 . September 2017 . 28578001 . 10.1016/j.jsbmb.2017.05.013 . 206502344 .
94. Dai W, Bai Y, Hebda L, Zhong X, Liu J, Kao J, Duan C . Calcium deficiency-induced and TRP channel-regulated IGF1R-PI3K-Akt signaling regulates abnormal epithelial cell proliferation . Cell Death and Differentiation . 21 . 4 . 568–81 . April 2014 . 24336047 . 3950320 . 10.1038/cdd.2013.177 .
95. Skrzypski M, Kołodziejski PA, Mergler S, Khajavi N, Nowak KW, Strowski MZ . TRPV6 modulates proliferation of human pancreatic neuroendocrine BON-1 tumour cells . Bioscience Reports . 36 . 4 . August 2016 . 27450545 . 4995500 . 10.1042/bsr20160106 .
96. Song H, Dong M, Zhou J, Sheng W, Li X, Gao W . Expression and prognostic significance of TRPV6 in the development and progression of pancreatic cancer . Oncology Reports . 39 . 3 . 1432–1440 . March 2018 . 29344675 . 10.3892/or.2018.6216 . free .
97. Chow J, Norng M, Zhang J, Chai J . TRPV6 mediates capsaicin-induced apoptosis in gastric cancer cells--Mechanisms behind a possible new "hot" cancer treatment . Biochimica et Biophysica Acta (BBA) - Molecular Cell Research . 1773 . 4 . 565–76 . April 2007 . 17292493 . 10.1016/j.bbamcr.2007.01.001 . free .
98. Zhang SS, Xie X, Wen J, Luo KJ, Liu QW, Yang H, Hu Y, Fu JH . 6 . TRPV6 plays a new role in predicting survival of patients with esophageal squamous cell carcinoma . Diagnostic Pathology . 11 . 1 . 14 . January 2016 . 26818094 . 4730645 . 10.1186/s13000-016-0457-7 . free .
99. Song Y, Peng X, Porta A, Takanaga H, Peng JB, Hediger MA, Fleet JC, Christakos S . 6 . Calcium transporter 1 and epithelial calcium channel messenger ribonucleic acid are differentially regulated by 1,25 dihydroxyvitamin D3 in the intestine and kidney of mice . Endocrinology . 144 . 9 . 3885–94 . September 2003 . 12933662 . 10.1210/en.2003-0314 . free .
100. Brown AJ, Krits I, Armbrecht HJ . Effect of age, vitamin D, and calcium on the regulation of rat intestinal epithelial calcium channels . Archives of Biochemistry and Biophysics . 437 . 1 . 51–8 . May 2005 . 15820216 . 10.1016/j.abb.2005.02.007 .
101. Meyer MB, Watanuki M, Kim S, Shevde NK, Pike JW . The human transient receptor potential vanilloid type 6 distal promoter contains multiple vitamin D receptor binding sites that mediate activation by 1,25-dihydroxyvitamin D3 in intestinal cells . Molecular Endocrinology . 20 . 6 . 1447–61 . June 2006 . 16574738 . 10.1210/me.2006-0031 . free .
102. Song Y, Kato S, Fleet JC . Vitamin D receptor (VDR) knockout mice reveal VDR-independent regulation of intestinal calcium absorption and ECaC2 and calbindin D9k mRNA . The Journal of Nutrition . 133 . 2 . 374–80 . February 2003 . 12566470 . 10.1093/jn/133.2.374 . free .
103. Christakos S, Dhawan P, Verstuyf A, Verlinden L, Carmeliet G . Vitamin D: Metabolism, Molecular Mechanism of Action, and Pleiotropic Effects . Physiological Reviews . 96 . 1 . 365–408 . January 2016 . 26681795 . 4839493 . 10.1152/physrev.00014.2015 .
104. Bouillon R, Van Cromphaut S, Carmeliet G . Intestinal calcium absorption: Molecular vitamin D mediated mechanisms . Journal of Cellular Biochemistry . 88 . 2 . 332–9 . February 2003 . 12520535 . 10.1002/jcb.10360 . 9853381 .
105. Replogle RA, Li Q, Wang L, Zhang M, Fleet JC . Gene-by-diet interactions influence calcium absorption and bone density in mice . Journal of Bone and Mineral Research . 29 . 3 . 657–65 . March 2014 . 23955923 . 10.1002/jbmr.2065 . 10591522 . 1546230 . free .
106. Van Cromphaut SJ, Rummens K, Stockmans I, Van Herck E, Dijcks FA, Ederveen AG, Carmeliet P, Verhaeghe J, Bouillon R, Carmeliet G . 6 . Intestinal calcium transporter genes are upregulated by estrogens and the reproductive cycle through vitamin D receptor-independent mechanisms . Journal of Bone and Mineral Research . 18 . 10 . 1725–36 . October 2003 . 14584880 . 10.1359/jbmr.2003.18.10.1725 . 25346500 . free .
107. Charoenphandhu N, Nakkrasae LI, Kraidith K, Teerapornpuntakit J, Thongchote K, Thongon N, Krishnamra N . Two-step stimulation of intestinal Ca(2+) absorption during lactation by long-term prolactin exposure and suckling-induced prolactin surge . American Journal of Physiology. Endocrinology and Metabolism . 297 . 3 . E609-19 . September 2009 . 19567804 . 10.1152/ajpendo.00347.2009 .
108. Beggs MR, Lee JJ, Busch K, Raza A, Dimke H, Weissgerber P, Engel J, Flockerzi V, Alexander RT . 6 . v1.3 Mediate Distal Small Intestine Calcium Absorption Before Weaning . Cellular and Molecular Gastroenterology and Hepatology . 8 . 4 . 625–642 . 2019 . 31398491 . 6889763 . 10.1016/j.jcmgh.2019.07.005 .
109. van Abel M, Huybers S, Hoenderop JG, van der Kemp AW, van Leeuwen JP, Bindels RJ . Age-dependent alterations in Ca2+ homeostasis: role of TRPV5 and TRPV6 . American Journal of Physiology. Renal Physiology . 291 . 6 . F1177-83 . December 2006 . 16705151 . 10.1152/ajprenal.00038.2006 .
110. Nie X, Jin H, Wen G, Xu J, An J, Liu X, Xie R, Tuo B . 6 . Estrogen Regulates Duodenal Calcium Absorption Through Differential Role of Estrogen Receptor on Calcium Transport Proteins . Digestive Diseases and Sciences . January 2020 . 65 . 12 . 3502–3513 . 31974908 . 10.1007/s10620-020-06076-x . 210862678 .
111. Lee BM, Lee GS, Jung EM, Choi KC, Jeung EB . Uterine and placental expression of TRPV6 gene is regulated via progesterone receptor- or estrogen receptor-mediated pathways during pregnancy in rodents . Reproductive Biology and Endocrinology . 7 . 1 . 49 . May 2009 . 19457270 . 2694200 . 10.1186/1477-7827-7-49 . free .
112. Park . Seon-Young . Yoo . Yeong-Min . Jung . Eui-Man . Jeung . Eui-Bae . The effect of steroid hormone on the expression of the calcium-processing proteins in the immature female rat brain . Journal of Chemical Neuroanatomy . April 2020 . 105 . 101767 . 10.1016/j.jchemneu.2020.101767. 32061997 . 211105316 .
113. Kim MH, Lee GS, Jung EM, Choi KC, Jeung EB . The negative effect of dexamethasone on calcium-processing gene expressions is associated with a glucocorticoid-induced calcium-absorbing disorder . Life Sciences . 85 . 3–4 . 146–52 . July 2009 . 19490920 . 10.1016/j.lfs.2009.05.013 .
114. Koo TH, Yang H, Jeung EB . 2011-07-01. Expression of Calcium Transport Genes in the Placenta of Calbindin-D9k and -D28k Knockout Mice.. Biology of Reproduction. 85. Suppl_1. 449. 10.1093/biolreprod/85.s1.449. 0006-3363.
115. Sopjani M, Kunert A, Czarkowski K, Klaus F, Laufer J, Föller M, Lang F . Regulation of the Ca(2+) channel TRPV6 by the kinases SGK1, PKB/Akt, and PIKfyve . The Journal of Membrane Biology . 233 . 1–3 . 35–41 . February 2010 . 20041238 . 10.1007/s00232-009-9222-0 . 25349984 .