Journal
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY
Volume 23, Issue 2, Pages 172-180Publisher
ACADEMIC PRESS LTD- ELSEVIER SCIENCE LTD
DOI: 10.1016/j.semcdb.2011.09.006
Keywords
Ca2+-induced Ca2+ release; IP3 receptor; NAADP; Ryanodine receptor; Store-operated Ca2+ entry; Two-pore channel
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Funding
- Wellcome Trust
- Medical Research Council
- Biotechnology and Biological Sciences Research Council
- BBSRC [BB/H009736/1] Funding Source: UKRI
- Biotechnology and Biological Sciences Research Council [1437702, BB/H009736/1] Funding Source: researchfish
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The ability of Ca2+, the simplest of all intracellular messengers, selectively to regulate so many cellular behaviours is due largely to the complex spatiotemporal organization of intracellular Ca2+ signals. Most signalling pathways, including those that culminate in Ca2+ signals, comprise sequences of protein-protein interactions linked by diffusible messengers. Using specific examples to illustrate key principles, we consider the roles of both components in defining the spatial organization of Ca2+ signals. We discuss evidence that regulation of most Ca2+ channels by Ca2+ contributes to controlling the duration of Ca2+ signals, to signal integration and, via Ca2+-induced Ca2+ release, to defining the spatial spread of Ca2+ signals. We distinguish two types of protein-protein interaction: scaffolds that allow rapid local transfer of diffusible messengers between signalling proteins, and interactions that directly transfer information between signalling proteins. Store-operated Ca2+ entry provides a ubiquitous example of the latter, and it serves also to illustrate how Ca2+ signals can be organized at different levels of spatial organization - from interactions between proteins to interactions between organelles. (C) 2011 Elsevier Ltd. All rights reserved.
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