Ca 2+ is an essential trigger for most forms of synaptic plasticity. Ca 2+ signaling occurs not only by Ca 2+ entry via plasma membrane channels but also via Ca 2+ signals generated by intracellular organelles. These organelles, by dynamically regulating the spatial and temporal extent of Ca 2+ 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 Ca 2+ stores, such as lysosomes, in neuronal Ca 2+ signaling and plasticity. We provide a comprehensive account of how Ca 2+ release from these stores regulates short- and long-term plasticity at the pre- and postsynaptic terminals of central synapses.
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Padamsey et al. (2018) studied this question.
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