| Literature DB >> 30819546 |
Yuanquan Song1, Dan Li2, Olivia Farrelly3, Leann Miles4, Feng Li2, Sung Eun Kim5, Tsz Y Lo6, Fei Wang7, Tun Li5, Katherine L Thompson-Peer5, Jiaxin Gong7, Swetha E Murthy8, Bertrand Coste8, Nikita Yakubovich9, Ardem Patapoutian8, Yang Xiang7, Panteleimon Rompolas3, Lily Yeh Jan10, Yuh Nung Jan11.
Abstract
Neurons exhibit a limited ability of repair. Given that mechanical forces affect neuronal outgrowth, it is important to investigate whether mechanosensitive ion channels may regulate axon regeneration. Here, we show that DmPiezo, a Ca2+-permeable non-selective cation channel, functions as an intrinsic inhibitor for axon regeneration in Drosophila. DmPiezo activation during axon regeneration induces local Ca2+ transients at the growth cone, leading to activation of nitric oxide synthase and the downstream cGMP kinase Foraging or PKG to restrict axon regrowth. Loss of DmPiezo enhances axon regeneration of sensory neurons in the peripheral and CNS. Conditional knockout of its mammalian homolog Piezo1 in vivo accelerates regeneration, while its pharmacological activation in vitro modestly reduces regeneration, suggesting the role of Piezo in inhibiting regeneration may be evolutionarily conserved. These findings provide a precedent for the involvement of mechanosensitive channels in axon regeneration and add a potential target for modulating nervous system repair.Entities:
Keywords: Drosophila; Piezo; axon regeneration; corneal sensory nerve; dendritic arborization neurons; ion channels; mammalian injury model; mechanosensitive; nitric oxide synthase
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Year: 2019 PMID: 30819546 PMCID: PMC6487666 DOI: 10.1016/j.neuron.2019.01.050
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173