Intracellular Ca2+ Release and Synaptic Plasticity: A Tale of Many Stores

Author:

Padamsey Zahid1ORCID,Foster William J.2,Emptage Nigel J.2

Affiliation:

1. Centre for Discovery Brain Sciences, Hugh Robson Building, University of Edinburgh, 15 George Square, Edinburgh, UK

2. Department of Pharmacology, University of Oxford, Mansfield Road, Oxford, Oxfordshire, UK

Abstract

Ca2+ is an essential trigger for most forms of synaptic plasticity. Ca2+ signaling occurs not only by Ca2+ entry via plasma membrane channels but also via Ca2+ signals generated by intracellular organelles. These organelles, by dynamically regulating the spatial and temporal extent of Ca2+ elevations within neurons, play a pivotal role in determining the downstream consequences of neural signaling on synaptic function. Here, we review the role of three major intracellular stores: the endoplasmic reticulum, mitochondria, and acidic Ca2+ stores, such as lysosomes, in neuronal Ca2+ signaling and plasticity. We provide a comprehensive account of how Ca2+ release from these stores regulates short- and long-term plasticity at the pre- and postsynaptic terminals of central synapses.

Publisher

SAGE Publications

Subject

Neurology (clinical),General Neuroscience

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