| Pacinian corpuscle | |
| Latin: | corpusculum Pacinian |
| Location: | Skin |
The Pacinian corpuscle, lamellar corpuscle or Vater-Pacini corpuscle[1] is one of the four major types of cutaneous receptor a type of mechanoreceptor (specialized receptor for mechanical sensation) found in mammalian skin. This type of mechanoreceptor is found in both hairy, and hairless skin, organs, joints, and attached to the periosteum of bone. Pacinian corpuscles are primarily responsible for sensitivity to vibration, and deep pressure.[1] A few are also sensitive to quasi-static or low frequency pressure stimuli. Most of them respond only to sudden disturbances and are especially sensitive to vibration of a few hundreds hertz.[2] The vibrational role may be used for detecting surface texture, such as rough and smooth. Most of the Pacinian corpuscles act as rapidly adapting mechanoreceptors. Groups of corpuscles respond to pressure changes, such as on grasping or releasing an object.
Pacinian corpuscles are larger and fewer in number than Meissner's corpuscle, Merkel cells and Ruffini's corpuscles.[3]
The Pacinian corpuscle is approximately oval-cylindrical-shaped and 1 mm in length. The entire corpuscle is wrapped by a layer of connective tissue. Its capsule consists of 20 to 60 concentric lamellae (hence the alternative lamellar corpuscle) including fibroblasts and fibrous connective tissue (mainly Type IV and Type II collagen network), separated by gelatinous material, more than 92% of which is water.[4] It presents a whorled pattern on micrographs.
Pacinian corpuscles are rapidly adapting (phasic) receptors that detect gross pressure changes and vibrations in the skin.[5] Any deformation in the corpuscle leads to opening of pressure-sensitive or stretch-activated ion channels or mechanosensitive channels present in the axon membrane or axolemma of the neurite inside the core of the corpuscles or end-organ. This initiates generation of the receptor potential inside the corpuscles which is also secondarily supported by the voltage-activated ion channels present in the core of the corpuscles. Finally the receptor potential is modulated to neural spikes or action potential with the help of opening of sodium ion channels present at the first Ranvier's Node of the axon.[2]
These corpuscles are especially sensitive to vibrations, which they can sense even centimeters away.[3] Their optimal sensitivity is 250 Hz, and this is the frequency range generated upon fingertips by textures made of features smaller than 1 μm.[6] [7] Pacinian corpuscles respond when the skin is rapidly indented but not when the pressure is steady, due to the layers of connective tissue that cover the nerve ending.[3] It is thought that they respond to high-velocity changes in joint position. They have also been implicated in detecting the location of touch sensations on handheld tools.[8]
Pacinian corpuscles have a large receptive field on the skin's surface with an especially sensitive center.[3]
Pacinian corpuscles sense stimuli due to the deformation of their lamellae, which press on the membrane of the sensory neuron and causes it to bend or stretch.[9] When the lamellae are deformed, due to either application or release of pressure, a generator or receptor potential is created as it physically deforms the plasma membrane of the receptive area of the neuron, making it "leak" different cations through Mechanosensitive channels which initiates the receptor potential. This mechanotransduction process is also supported by distributed voltage sensitive ion channels in the inner-core and neurite of the corpuscles.[2] Due to generation of receptor potential in the receptive area of the neurite (especially near the heminode or half-node of the axon) the potential at the first Ranvier's node can reach certain threshold, triggering nerve impulses or action potentials at the first node of Ranvier. The first Ranvier's node of the myelinated section of the neurite is often found inside the capsule. This impulse is then transferred along the axon from node to node with the use of sodium channels and sodium/potassium pumps in the axon membrane.
Once the receptive area of the neurite is depolarized, it will depolarize the first node of Ranvier; however, as it is a rapidly adapting fibre, this does not carry on indefinitely, and the signal propagation ceases. This is a graded response, meaning that the greater the deformation, the greater the generator potential. This information is encoded in the frequency of impulses, since a bigger or faster deformation induces a higher impulse frequency. Action potentials are formed when the skin is rapidly distorted but not when pressure is continuous because of the mechanical filtering of the stimulus in the lamellar structure. The frequencies of the impulses decrease quickly and soon stop due to the relaxation of the inner layers of connective tissue that cover the nerve ending.
Pacinian corpuscles were the first cellular sensory receptor ever observed. They were first reported by German anatomist and botanist Abraham Vater and his student Johannes Gottlieb Lehmann in 1741, but ultimately named after Italian anatomist Filippo Pacini, who rediscovered them in 1835.[10] [11] John Shekleton, a curator of the Royal College of Surgeons in Ireland, also discovered them before Pacini, but his results were published later. Similar to Pacinian corpuscles, Herbst corpuscles and Grandry corpuscles are found in bird species.