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Activating injury-responsive genes with hypoxia enhances axon regeneration through neuronal HIF-1α

ABSTRACT: Injured peripheral neurons successfully activate a pro-regenerative transcriptional program to enable axon regeneration and functional recovery. How transcriptional regulators coordinate the expression of such programs remains unclear. Here we show that hypoxia-inducible factor 1α (HIF-1α) controls multiple injury-induced genes in sensory neurons and contribute to the pre-conditioning lesion effect. Knockdown of HIF-1α in vitro or conditional knockout in vivo impairs sensory axon regeneration. The HIF-1α target gene Vascular Endothelial Growth Factor A (VEGFA) is expressed in injured neurons and contributes to stimulate axon regeneration. Induction of HIF-1α using hypoxia enhances axon regeneration in vitro and in vivo in sensory neurons. Hypoxia also stimulates motor neuron regeneration and accelerates neuromuscular junction reinnervation. This study demonstrates that HIF-1α represents a critical transcriptional regulator in regenerating neurons and suggests hypoxia as a tool to stimulate axon regeneration.

ORGANISM(S): Mus musculus

PROVIDER: GSE73415 | GEO | 2016/01/21

SECONDARY ACCESSION(S): PRJNA296908

REPOSITORIES: GEO

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Project description:Activating injury-responsive genes with hypoxia enhances axon regeneration through neuronal HIF-1α

| PRJNA296908 | ENA

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