<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>2(10)</volume><submitter>Gees M</submitter><pubmed_abstract>The 28 mammalian members of the super-family of transient receptor potential (TRP) channels are cation channels, mostly permeable to both monovalent and divalent cations, and can be subdivided into six main subfamilies: the TRPC (canonical), TRPV (vanilloid), TRPM (melastatin), TRPP (polycystin), TRPML (mucolipin), and the TRPA (ankyrin) groups. TRP channels are widely expressed in a large number of different tissues and cell types, and their biological roles appear to be equally diverse. In general, considered as polymodal cell sensors, they play a much more diverse role than anticipated. Functionally, TRP channels, when activated, cause cell depolarization, which may trigger a plethora of voltage-dependent ion channels. Upon stimulation, Ca2+ permeable TRP channels generate changes in the intracellular Ca2+ concentration, [Ca2+]i, by Ca2+ entry via the plasma membrane. However, more and more evidence is arising that TRP channels are also located in intracellular organelles and serve as intracellular Ca2+ release channels. This review focuses on three major tasks of TRP channels: (1) the function of TRP channels as Ca2+ entry channels; (2) the electrogenic actions of TRPs; and (3) TRPs as Ca2+ release channels in intracellular organelles.</pubmed_abstract><journal>Cold Spring Harbor perspectives in biology</journal><pagination>a003962</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2944357</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The role of transient receptor potential cation channels in Ca2+ signaling.</pubmed_title><pmcid>PMC2944357</pmcid><pubmed_authors>Colsoul B</pubmed_authors><pubmed_authors>Nilius B</pubmed_authors><pubmed_authors>Gees M</pubmed_authors></additional><is_claimable>false</is_claimable><name>The role of transient receptor potential cation channels in Ca2+ signaling.</name><description>The 28 mammalian members of the super-family of transient receptor potential (TRP) channels are cation channels, mostly permeable to both monovalent and divalent cations, and can be subdivided into six main subfamilies: the TRPC (canonical), TRPV (vanilloid), TRPM (melastatin), TRPP (polycystin), TRPML (mucolipin), and the TRPA (ankyrin) groups. TRP channels are widely expressed in a large number of different tissues and cell types, and their biological roles appear to be equally diverse. In general, considered as polymodal cell sensors, they play a much more diverse role than anticipated. Functionally, TRP channels, when activated, cause cell depolarization, which may trigger a plethora of voltage-dependent ion channels. Upon stimulation, Ca2+ permeable TRP channels generate changes in the intracellular Ca2+ concentration, [Ca2+]i, by Ca2+ entry via the plasma membrane. However, more and more evidence is arising that TRP channels are also located in intracellular organelles and serve as intracellular Ca2+ release channels. This review focuses on three major tasks of TRP channels: (1) the function of TRP channels as Ca2+ entry channels; (2) the electrogenic actions of TRPs; and (3) TRPs as Ca2+ release channels in intracellular organelles.</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Oct</publication><modification>2024-11-20T05:49:32.524Z</modification><creation>2019-06-06T22:22:00Z</creation></dates><accession>S-EPMC2944357</accession><cross_references><pubmed>20861159</pubmed><doi>10.1101/cshperspect.a003962</doi></cross_references></HashMap>