Bcl-xL explained

B-cell lymphoma-extra large (Bcl-xL), encoded by the BCL2-like 1 gene, is a transmembrane molecule in the mitochondria. It is a member of the Bcl-2 family of proteins, and acts as an anti-apoptotic protein by preventing the release of mitochondrial contents such as cytochrome c, which leads to caspase activation and ultimately, programmed cell death.[1]

Function

It is a well-established concept in the field of apoptosis that relative amounts of pro- and anti-survival Bcl-2 family of proteins determine whether the cell will undergo cell death; if more Bcl-xL is present, then pores are non-permeable to pro-apoptotic molecules and the cell survives. However, if Bax and Bak become activated, and Bcl-xL is sequestered away by gatekeeper BH3-only factors (e.g. Bim) causing a pore to form, cytochrome c is released leading to initiation of caspase cascade and apoptotic events.[2]

While the exact signaling pathway of Bcl-xL is still not known, it is believed that Bcl-xL differs highly from Bcl-2 in their mechanism of inducing apoptosis. Bcl-xL is about ten times more functional than Bcl-2 when induced by the chemotherapy drug, Doxorubicin[3] and can specifically bind to cytochrome C residues, preventing apoptosis.[4] It can also prevent the formation of Apaf-1 and Caspase 9 complex by acting directly upon Apaf-1 rather than Caspase 9, as shown in nematode homologs.[5]

Clinical significance

Bcl-xL dysfunction in mice can cause ineffective production of red blood cells, severe anemia, hemolysis, and death. This protein has also been shown as a requirement for heme production[6] and in erythroid lineage, Bcl-xL is a major survival factor responsible for an estimated half of the total survival "signal" proerythroblasts must receive in order to survive and become red cells. Bcl-xL promoter contains GATA-1 and Stat5 sites. This protein accumulates throughout the differentiation, ensuring the survival of erythroid progenitors. Because iron metabolism and incorporation into hemoglobin occurs inside the mitochondria, Bcl-xL was suggested to play additional roles in regulating this process in erythrocytes which could lead to a role in polycythemia vera, a disease where there is an overproduction of erythrocytes.[7]

Similar to other Bcl-2 family members, Bcl-xL has been implicated in the survival of cancer cells by inhibiting the function of p53, a tumor suppressor. In cancerous mouse cells, those which contained Bcl-xL were able to survive while those that only expressed p53 died in a small period of time.[8]

Bcl-xL is a target of various senolytic agents. Studies of cell cultures of senescent human umbilical vein endothelial cells have shown that both fisetin and quercetin induce apoptosis by inhibition of Bcl-xL.[9] Fisetin has roughly twice the senolytic potency as quercetin.[10]

Related proteins

Other Bcl-2 proteins include Bcl-2, Bcl-w, Bcl-xs, and Mcl-1.

Notes and References

  1. Korsmeyer SJ . Regulators of cell death . Trends in Genetics . 11 . 3 . 101–105 . March 1995 . 7732571 . 10.1016/S0168-9525(00)89010-1 .
  2. Finucane DM, Bossy-Wetzel E, Waterhouse NJ, Cotter TG, Green DR . Bax-induced caspase activation and apoptosis via cytochrome c release from mitochondria is inhibitable by Bcl-xL . The Journal of Biological Chemistry . 274 . 4 . 2225–2233 . January 1999 . 9890985 . 10.1074/jbc.274.4.2225 . free .
  3. Fiebig AA, Zhu W, Hollerbach C, Leber B, Andrews DW . Bcl-XL is qualitatively different from and ten times more effective than Bcl-2 when expressed in a breast cancer cell line . BMC Cancer . 6 . 213 . 213 . August 2006 . 16928273 . 1560389 . 10.1186/1471-2407-6-213 . free .
  4. Bertini I, Chevance S, Del Conte R, Lalli D, Turano P . The anti-apoptotic Bcl-x(L) protein, a new piece in the puzzle of cytochrome c interactome . PLOS ONE . 6 . 4 . e18329 . April 2011 . 21533126 . 3080137 . 10.1371/journal.pone.0018329 . 2011PLoSO...618329B . free .
  5. Hu Y, Benedict MA, Wu D, Inohara N, Núñez G . Bcl-XL interacts with Apaf-1 and inhibits Apaf-1-dependent caspase-9 activation . Proceedings of the National Academy of Sciences of the United States of America . 95 . 8 . 4386–4391 . April 1998 . 9539746 . 22498 . 10.1073/pnas.95.8.4386 . 1998PNAS...95.4386H . free .
  6. Rhodes MM, Kopsombut P, Bondurant MC, Price JO, Koury MJ . Bcl-x(L) prevents apoptosis of late-stage erythroblasts but does not mediate the antiapoptotic effect of erythropoietin . Blood . 106 . 5 . 1857–1863 . September 2005 . 15899920 . 1895223 . 10.1182/blood-2004-11-4344 .
  7. Silva M, Richard C, Benito A, Sanz C, Olalla I, Fernández-Luna JL . Expression of Bcl-x in erythroid precursors from patients with polycythemia vera . The New England Journal of Medicine . 338 . 9 . 564–571 . February 1998 . 9475763 . 10.1056/NEJM199802263380902 . free .
  8. Schott AF, Apel IJ, Nuñez G, Clarke MF . Bcl-XL protects cancer cells from p53-mediated apoptosis . Oncogene . 11 . 7 . 1389–1394 . October 1995 . 7478561 .
  9. Kirkland JL, Tchkonia T . Senolytic drugs: from discovery to translation . Journal of Internal Medicine . 288 . 5 . 518–536 . November 2020 . 32686219 . 7405395 . 10.1111/joim.13141 .
  10. Wyld L, Bellantuono I, Tchkonia T, Morgan J, Turner O, Foss F, George J, Danson S, Kirkland JL . 6 . Senescence and Cancer: A Review of Clinical Implications of Senescence and Senotherapies . Cancers . 12 . 8 . e2134 . July 2020 . 32752135 . 7464619 . 10.3390/cancers12082134 . free .