| Literature DB >> 30049781 |
Tongtong Zhao1,2, Yingsong Hao1,2, Joshua M Kaplan3,4.
Abstract
Neurons are highly dependent on mitochondrial function, and mitochondrial damage has been implicated in many neurological and neurodegenerative diseases. Here we show that axonal mitochondria are necessary for neuropeptide secretion in Caenorhabditis elegans and that oxidative phosphorylation, but not mitochondrial calcium uptake, is required for secretion. Oxidative phosphorylation produces cellular ATP, reactive oxygen species, and consumes oxygen. Disrupting any of these functions could inhibit neuropeptide secretion. We show that blocking mitochondria transport into axons or decreasing mitochondrial function inhibits neuropeptide secretion through activation of the hypoxia inducible factor HIF-1 Our results suggest that axonal mitochondria modulate neuropeptide secretion by regulating transcriptional responses induced by metabolic stress.Entities:
Keywords: Caenorhabditis elegans; hypoxia; mitochondria; neuropeptide secretion; reactive oxygen species
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Year: 2018 PMID: 30049781 PMCID: PMC6116974 DOI: 10.1534/genetics.118.301014
Source DB: PubMed Journal: Genetics ISSN: 0016-6731 Impact factor: 4.562