Mitochondrial calcium uptake modulates synaptic vesicle endocytosis in central nerve terminals

Jamie Marland, Philip Hasel, Katherine Bonnycastle , Michael Cousin

Research output: Contribution to journalArticlepeer-review

Abstract

Presynaptic calcium influx triggers synaptic vesicle (SV) exocytosis and modulates subsequent SV endocytosis. A number of calcium clearance mechanisms are present in central nerve terminals which regulate intracellular free calcium levels both during and after stimulation. During action potential stimulation mitochondria rapidly accumulate presynaptic calcium via the mitochondrial calcium uniporter (MCU). The role of mitochondrial calcium uptake in modulating SV recycling has been extensively debated; however a definitive conclusion has not been achieved. To directly address this question we manipulated the expression of the MCU channel subunit in primary cultures of neurons expressing a genetically-encoded reporter of SV turnover. Knockdown of MCU resulted in ablation of activity-dependent mitochondrial calcium uptake but had no effect on either the rate or extent of SV exocytosis. In contrast, the rate of SV endocytosis was increased in the absence of mitochondrial calcium uptake and slowed when MCU was overexpressed. MCU knockdown did not perturb activity-dependent increases in presynaptic free calcium, suggesting that SV endocytosis may be controlled by calcium accumulation and efflux from mitochondria in their immediate vicinity.
Original languageEnglish
Pages (from-to)2080-2086
JournalJournal of Biological Chemistry
Volume291
Issue number5
Early online date7 Dec 2015
DOIs
Publication statusPublished - 29 Jan 2016

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