Document Detail


Store-operated Ca2+ entry: dynamic interplay between endoplasmic reticulum, mitochondria and plasma membrane.
MedLine Citation:
PMID:  12576497     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
In eukaryotic cells, hormones and neurotransmitters that engage the phosphoinositide pathway evoke a biphasic increase in intracellular free Ca2+ concentration: an initial transient release of Ca2+ from intracellular stores is followed by a sustained phase of Ca2+ influx. This influx is generally store-dependent and is required for controlling a host of Ca2+-dependent processes ranging from exocytosis to cell growth and proliferation. In many cell types, store-operated Ca2+ entry is manifest as a non-voltage-gated Ca2+ current called ICRAC (Ca2+ release-activated Ca2+ current). Just how store emptying activates CRAC channels remains unclear, and some of our recent experiments that address this issue will be described. No less important from a physiological perspective is the weak Ca2+ buffer paradox: whereas macroscopic (whole cell) ICRAC can be measured routinely in the presence of strong intracellular Ca2+ buffer, the current is generally not detectable under physiological conditions of weak buffering following store emptying with the second messenger InsP3. In this review, I describe some of our experiments aimed at understanding just why InsP3 is ineffective under these conditions and which lead us to conclude that respiring mitochondria are essential for the activation of ICRAC in weak intracellular Ca2+ buffer. Mitochondrial Ca2+ uptake also increases the dynamic range over which InsP3 functions as the second messenger that controls Ca2+ influx. Finally, we find that Ca2+-dependent slow inactivation of Ca2+ influx, a widespread but poorly understood phenomenon that helps shape the profile of an intracellular Ca2+ signal, is regulated by mitochondrial Ca2+ buffering. Thus, by enabling macroscopic store-operated Ca2+ current to activate and then by controlling its extent and duration, mitochondria play a crucial role in all stages of store-operated Ca2+ influx. Store-operated Ca2+ entry reflects therefore a dynamic interplay between endoplasmic reticulum, mitochondria and plasma membrane.
Authors:
Anant B Parekh
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Publication Detail:
Type:  Lectures; Research Support, Non-U.S. Gov't     Date:  2003-02-07
Journal Detail:
Title:  The Journal of physiology     Volume:  547     ISSN:  0022-3751     ISO Abbreviation:  J. Physiol. (Lond.)     Publication Date:  2003 Mar 
Date Detail:
Created Date:  2003-03-03     Completed Date:  2003-09-23     Revised Date:  2013-06-09    
Medline Journal Info:
Nlm Unique ID:  0266262     Medline TA:  J Physiol     Country:  England    
Other Details:
Languages:  eng     Pagination:  333-48     Citation Subset:  IM    
Affiliation:
Department of Physiology, University of Oxford, Parks Road, Oxford OX1 3PT, UK. anant.parekh@physiol.ox.ac.uk
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MeSH Terms
Descriptor/Qualifier:
Animals
Buffers
Calcium / metabolism*
Calcium Channels / physiology
Calcium-Transporting ATPases / metabolism
Cell Membrane / metabolism
Cytosol / metabolism
Electric Conductivity
Endoplasmic Reticulum / metabolism*
Humans
Inositol 1,4,5-Trisphosphate / physiology
Mitochondria / metabolism*,  physiology
Oxygen Consumption
Chemical
Reg. No./Substance:
0/Buffers; 0/Calcium Channels; 7440-70-2/Calcium; 85166-31-0/Inositol 1,4,5-Trisphosphate; EC 3.6.3.8/Calcium-Transporting ATPases
Comments/Corrections

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