Calcium channel

Source: Wikipedia, the free encyclopedia.

A calcium 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.    

Comparison tables

The following tables explain gating, gene, location and function of different types of calcium channels, both voltage and ligand-gated.

Voltage-gated

Main article: voltage-gated calcium channel
  • voltage-operated calcium channels
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
Cav3.2 (CACNA1H)
Cav3.3 (CACNA1I
)		 neurons, cells that have
osteocytes), thalamus (thalamus
)

Ligand-gated

  • receptor-operated calcium channels
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 receptors in T-tubules
and increased intracellular calcium (Calcium Induced Calcium Release - CICR)		 RYR1, RYR2, RYR3 ER/SR
myocytes[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]

Non-selective Channels Permeable to Calcium

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]

Pharmacology

Depiction of binding sites of various antagonistic drugs in the L-type calcium channel.

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

References

  1. ^ "calcium channel" at Dorland's Medical Dictionary
  2. PMID 8791458
    .
  3. PMID 29131938
    .
  4. ^
    ISBN 978-0-443-07145-4
    .
  5. ^ "TPCN1 - Two pore calcium channel protein 1 - Homo sapiens (Human) - TPCN1 gene & protein". www.uniprot.org. Retrieved 2017-12-11.
  6. PMID 26400989
    .
  7. PMID 27913208
    .
  8. S2CID 259784278
    .
  9. S2CID 22271779
    .
  10. PMID 3540226
    .
  11. PMID 20091047
    .

External links
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