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Ca(2+) Channels on the Move

[Image: see text] The versatility of Ca(2+) as an intracellular messenger derives largely from the spatial organization of cytosolic Ca(2+) signals, most of which are generated by regulated openings of Ca(2+)-permeable channels. Most Ca(2+) channels are expressed in the plasma membrane (PM). Others,...

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Detalles Bibliográficos
Autores principales: Taylor, Colin W., Prole, David L., Rahman, Taufiq
Formato: Texto
Lenguaje:English
Publicado: American Chemical Society 2009
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797372/
https://www.ncbi.nlm.nih.gov/pubmed/19928968
http://dx.doi.org/10.1021/bi901739t
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author Taylor, Colin W.
Prole, David L.
Rahman, Taufiq
author_facet Taylor, Colin W.
Prole, David L.
Rahman, Taufiq
author_sort Taylor, Colin W.
collection PubMed
description [Image: see text] The versatility of Ca(2+) as an intracellular messenger derives largely from the spatial organization of cytosolic Ca(2+) signals, most of which are generated by regulated openings of Ca(2+)-permeable channels. Most Ca(2+) channels are expressed in the plasma membrane (PM). Others, including the almost ubiquitous inositol 1,4,5-trisphosphate receptors (IP(3)R) and their relatives, the ryanodine receptors (RyR), are predominantly expressed in membranes of the sarcoplasmic or endoplasmic reticulum (ER). Targeting of these channels to appropriate destinations underpins their ability to generate spatially organized Ca(2+) signals. All Ca(2+) channels begin life in the cytosol, and the vast majority are then functionally assembled in the ER, where they may either remain or be dispatched to other membranes. Here, by means of selective examples, we review two issues related to this trafficking of Ca(2+) channels via the ER. How do cells avoid wayward activity of Ca(2+) channels in transit as they pass from the ER via other membranes to their final destination? How and why do some cells express small numbers of the archetypal intracellular Ca(2+) channels, IP(3)R and RyR, in the PM?
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spelling pubmed-27973722009-12-23 Ca(2+) Channels on the Move Taylor, Colin W. Prole, David L. Rahman, Taufiq Biochemistry [Image: see text] The versatility of Ca(2+) as an intracellular messenger derives largely from the spatial organization of cytosolic Ca(2+) signals, most of which are generated by regulated openings of Ca(2+)-permeable channels. Most Ca(2+) channels are expressed in the plasma membrane (PM). Others, including the almost ubiquitous inositol 1,4,5-trisphosphate receptors (IP(3)R) and their relatives, the ryanodine receptors (RyR), are predominantly expressed in membranes of the sarcoplasmic or endoplasmic reticulum (ER). Targeting of these channels to appropriate destinations underpins their ability to generate spatially organized Ca(2+) signals. All Ca(2+) channels begin life in the cytosol, and the vast majority are then functionally assembled in the ER, where they may either remain or be dispatched to other membranes. Here, by means of selective examples, we review two issues related to this trafficking of Ca(2+) channels via the ER. How do cells avoid wayward activity of Ca(2+) channels in transit as they pass from the ER via other membranes to their final destination? How and why do some cells express small numbers of the archetypal intracellular Ca(2+) channels, IP(3)R and RyR, in the PM? American Chemical Society 2009-11-24 2009-12-29 /pmc/articles/PMC2797372/ /pubmed/19928968 http://dx.doi.org/10.1021/bi901739t Text en Copyright © 2009 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org.
spellingShingle Taylor, Colin W.
Prole, David L.
Rahman, Taufiq
Ca(2+) Channels on the Move
title Ca(2+) Channels on the Move
title_full Ca(2+) Channels on the Move
title_fullStr Ca(2+) Channels on the Move
title_full_unstemmed Ca(2+) Channels on the Move
title_short Ca(2+) Channels on the Move
title_sort ca(2+) channels on the move
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2797372/
https://www.ncbi.nlm.nih.gov/pubmed/19928968
http://dx.doi.org/10.1021/bi901739t
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