Mitochondria promote neuropeptide secretion inCaenorhabditis elegansby preventing activation of hypoxia inducible factor

Abstract

Neurons are highly dependent on mitochondrial function, and mitochondrial damage has been implicated in many neurological and neurodegenerative diseases. Relatively little is known about how mitochondria regulate neuronal function. 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 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. 6 MATERIALS AND METHODS C. elegans strains and drug assaysStrains were maintained at 20°C as described (BRENNER 1974). The wild-type reference strain was N2 Bristol. Full descriptions of all alleles can be found at http://www.wormbase.org. Strains used in this study are as follows:KP8711 ric-7(