Ion channel complex through which calcium ions pass
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.
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]
^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.
^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.
^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.
^Katz AM (September 1986). "Pharmacology and mechanisms of action of calcium-channel blockers". Journal of Clinical Hypertension. 2 (3 Suppl): 28S–37S. PMID 3540226.
^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
"The Weiss Lab". The Weiss Lab is investigating the molecular and cellular mechanisms underlying human diseases caused by dysfunction of ion channels.
"Voltage-Gated Ion Channels". IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology. Archived from the original on 2021-04-17. Retrieved 2008-12-17.
"TRIP Database". a manually curated database of protein-protein interactions for mammalian TRP channels. Archived from the original on 2016-08-10. Retrieved 2021-06-18.