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Calcium channel

From Wikipedia, the free encyclopedia
Ion channel complex through which calcium ions pass

Acalcium channel is anion channel which shows selective permeability tocalcium ions. It is sometimes synonymous withvoltage-gated calcium channel,[1] which are a type of calcium channel regulated by changes inmembrane potential. Some calcium channels are regulated by the binding of aligand.[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 ofaction potentials across cell membranes. Calcium channels can also be used to release calcium ions assecond messengers within the cell, affecting downstream signaling pathways.   

Comparison tables

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

Voltage-gated

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Main article:voltage-gated calcium channel
  • voltage-operated calcium channels
TypeVoltageα1 subunit (gene name)Associated subunitsMost 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, γSkeletal 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 γThroughout thebrain and peripheral nervous system.
P-type calcium channel ("Purkinje") /Q-type calcium channelHVA (high voltage activated)Cav2.1 (CACNA1A)α2δ, β, possibly γPurkinje neurons in the cerebellum /Cerebellargranule cells
R-type calcium channel ("Residual")intermediate-voltage-activatedCav2.3 (CACNA1E)α2δ, β, possibly γCerebellargranule cells, other neurons
T-type calcium channel ("Transient")low-voltage-activatedCav3.1 (CACNA1G)
Cav3.2 (CACNA1H)
Cav3.3 (CACNA1I)
Cells that havepacemaker activity in heart, neurons, thalamus (thalamus), bone (osteocytes)

Ligand-gated

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  • receptor-operated calcium channels
TypeGated byGeneLocationFunction
IP3 receptorIP3ITPR1, ITPR2, ITPR3ER/SRReleases calcium from ER/SR in response to IP3 by e.g.GPCRs[4]
Ryanodine receptordihydropyridine receptors inT-tubules and increased intracellular calcium (Calcium Induced Calcium Release - CICR)RYR1, RYR2, RYR3ER/SRCalcium-induced calcium release inmyocytes[4]
Two-pore channelNicotinic acid adenine dinucleotide phosphate (NAADP)TPCN1, TPCN2endosomal/lysosomal membranesNAADP-activated calcium transport across endosomal/lysosomal membranes[5]
store-operated channels[6]indirectly byER/SR depletion of calcium[4]ORAI1, ORAI2, ORAI3plasma membraneProvides calcium signaling to the cytoplasm[7]

Non-selective channels permeable to calcium

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There are several cation channel families that allow positively charged ions including calcium to pass through. These includeP2X receptors,Transient Receptor Potential (TRP) channels,Cyclic nucleotide-gated (CNG) channels,Acid-sensing ion channels, andSOC 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

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

L-typecalcium channel blockers are used to treathypertension. 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-typecalcium channel blockers are used to treatepilepsy. 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

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References

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  1. ^"calcium channel" atDorland's Medical Dictionary
  2. ^Striggow F, Ehrlich BE (August 1996). "Ligand-gated calcium channels inside and out".Current Opinion in Cell Biology.8 (4): 490–495.doi:10.1016/S0955-0674(96)80025-1.PMID8791458.
  3. ^Zamponi, Gerald W. (2017-12-20)."A Crash Course in Calcium Channels".ACS Chemical Neuroscience.8 (12):2583–2585.doi:10.1021/acschemneuro.7b00415.ISSN 1948-7193.PMID 29131938.
  4. ^abcRang HP (2003).Pharmacology. Edinburgh: Churchill Livingstone. p. 54.ISBN 978-0-443-07145-4.
  5. ^"TPCN1 - Two pore calcium channel protein 1 - Homo sapiens (Human) - TPCN1 gene & protein".www.uniprot.org. Retrieved2017-12-11.
  6. ^Prakriya, Murali; Lewis, Richard S. (Oct 2015)."Store-Operated Calcium Channels".Physiological Reviews.95 (4):1383–1436.doi:10.1152/physrev.00020.2014.ISSN 0031-9333.PMC 4600950.PMID 26400989.
  7. ^Putney JW, Steinckwich-Besançon N, Numaga-Tomita T, Davis FM, Desai PN, D'Agostin DM, et al. (June 2017)."The functions of store-operated calcium channels".Biochimica et Biophysica Acta (BBA) - Molecular Cell Research.1864 (6):900–906.doi:10.1016/j.bbamcr.2016.11.028.PMC 5420336.PMID 27913208.
  8. ^Zheng, Jie; Trudeau, Matthew C. (2023-06-06).Textbook of Ion Channels Volume II: Properties, Function, and Pharmacology of the Superfamilies (1 ed.). Boca Raton: CRC Press.doi:10.1201/9781003096276.ISBN 978-1-003-09627-6.S2CID 259784278.
  9. ^Wu, Jianping; Yan, Zhen; Li, Zhangqiang; Yan, Chuangye; Lu, Shan; Dong, Mengqiu; Yan, Nieng (2015-12-18)."Structure of the voltage-gated calcium channel Ca v 1.1 complex".Science.350 (6267) aad2395.doi:10.1126/science.aad2395.ISSN 0036-8075.PMID 26680202.S2CID 22271779.
  10. ^Katz AM (September 1986). "Pharmacology and mechanisms of action of calcium-channel blockers".Journal of Clinical Hypertension.2 (3 Suppl):28S –37S.PMID 3540226.
  11. ^Zamponi GW, Lory P, Perez-Reyes E (July 2010)."Role of voltage-gated calcium channels in epilepsy".Pflügers Archiv.460 (2):395–403.doi:10.1007/s00424-009-0772-x.PMC 3312315.PMID 20091047.

External links

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Ligand-gated
Voltage-gated
Constitutively active
Proton-gated
Voltage-gated
Calcium-activated
Inward-rectifier
Tandem pore domain
Voltage-gated
Miscellaneous
Cl:Chloride channel
H+:Proton channel
M+:CNG cation channel
M+:TRP cation channel
H2O (+solutes):Porin
Cytoplasm:Gap junction
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Ion channel class
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