Acalcium channel is an ion channel which shows selective permeability to calcium ions. It is sometimes synonymous with voltage-gated calcium channel,[1] which are a type of calcium channel regulated by changes in membrane potential. Some calcium channels are regulated by the binding of a ligand.[2][3] Other calcium channels can also be regulated by both voltage and ligands to provide precise control over ion flow. Some cation channels allow calcium as well as other cations to pass through the membrane.
Calcium channels can participate in the creation of action potentials across cell membranes. Calcium channels can also be used to release calcium ions as second messengers within the cell, affecting downstream signaling pathways.
The following tables explain gating, gene, location and function of different types of calcium channels, both voltage and ligand-gated.
| Type | Voltage | α1 subunit (gene name) | Associated subunits | Most often found in |
| L-type calcium channel ("Long-Lasting" AKA "DHP Receptor") | HVA (high voltage activated) | Cav1.1 (CACNA1S) Cav1.2 (CACNA1C) Cav1.3 (CACNA1D) Cav1.4 (CACNA1F) |
α2δ, β, γ | Skeletal muscle, smooth muscle, bone (osteoblasts), ventricular myocytes** (responsible for prolonged action potential in cardiac cell; also termed DHP receptors), dendrites and dendritic spines of cortical neurons |
| N-type calcium channel ("Neural"/"Non-L") | HVA (high-voltage-activated) | Cav2.2 (CACNA1B) | α2δ/β1, β3, β4, possibly γ | Throughout the brain and peripheral nervous system. |
| P-type calcium channel ("Purkinje") /Q-type calcium channel | HVA (high voltage activated) | Cav2.1 (CACNA1A) | α2δ, β, possibly γ | Purkinje neurons in the cerebellum / Cerebellar granule cells |
| R-type calcium channel ("Residual") | intermediate-voltage-activated | Cav2.3 (CACNA1E) | α2δ, β, possibly γ | Cerebellar granule cells, other neurons |
| T-type calcium channel ("Transient") | low-voltage-activated | Cav3.1 (CACNA1G) Cav3.2 (CACNA1H) Cav3.3 (CACNA1I) |
neurons, cells that have pacemaker activity, bone (osteocytes), thalamus (thalamus) |
| Type | Gated by | Gene | Location | Function |
| IP3 receptor | IP3 | ITPR1, ITPR2, ITPR3 | ER/SR | Releases calcium from ER/SR in response to IP3 by e.g. GPCRs[4] |
| Ryanodine receptor | dihydropyridine receptorsinT-tubules and increased intracellular calcium (Calcium Induced Calcium Release - CICR) | RYR1, RYR2, RYR3 | ER/SR | Calcium-induced calcium releaseinmyocytes[4] |
| Two-pore channel | Nicotinic acid adenine dinucleotide phosphate (NAADP) | TPCN1, TPCN2 | endosomal/lysosomal membranes | NAADP-activated calcium transport across endosomal/lysosomal membranes[5] |
| store-operated channels[6] | indirectly by ER/SR depletion of calcium[4] | ORAI1, ORAI2, ORAI3 | plasma membrane | Provides calcium signaling to the cytoplasm[7] |
There are several cation channel families that allow positively charged ions including calcium to pass through. These include P2X receptors, Transient Receptor Potential (TRP) channels, Cyclic nucleotide-gated (CNG) channels, Acid-sensing ion channels, and SOC channels.[8] These channels can be regulated by membrane voltage potentials, ligands, and/or other cellular conditions. Cat-Sper channels, found in mammalian sperm, are one example of this as they are voltage gated and ligand regulated.[9]
L-type calcium channel blockers are used to treat hypertension. In most areas of the body, depolarization is mediated by sodium influx into a cell; changing the calcium permeability has little effect on action potentials. However, in many smooth muscle tissues, depolarization is mediated primarily by calcium influx into the cell. L-type calcium channel blockers selectively inhibit these action potentials in smooth muscle which leads to dilation of blood vessels; this in turn corrects hypertension.[10]
T-type calcium channel blockers are used to treat epilepsy. Increased calcium conductance in the neurons leads to increased depolarization and excitability. This leads to a greater predisposition to epileptic episodes. Calcium channel blockers reduce the neuronal calcium conductance and reduce the likelihood of experiencing epileptic attacks.[11]
|
| |||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| |||||||||||||||||
| |||||||||||||||||
| |||||||||||||||||
| |||||||||||||||||
| |||||||||||||||||
see also disorders | |||||||||||||||||
