| Literature DB >> 28768198 |
Véronique Lisi1, Bhagat Singh2, Michel Giroux1, Elmer Guzman1, Michio W Painter2, Yung-Chih Cheng2, Eric Huebner2, Giovanni Coppola3, Michael Costigan4, Clifford J Woolf2, Kenneth S Kosik5.
Abstract
Peripheral nerve regeneration after injury requires a broad program of transcriptional changes. We investigated the basis for the enhanced nerve regenerative capacity of the CAST/Ei mouse strain relative to C57BL/6 mice. RNA sequencing of dorsal root ganglia (DRG) showed a CAST/Ei-specific upregulation of Ascl1 after injury. Ascl1 overexpression in DRG neurons of C57BL/6 mice enhanced their neurite outgrowth. Ascl1 is regulated by miR-7048-3p, which is downregulated in CAST/Ei mice. Inhibition of miR-7048-3p enhances neurite outgrowth. Following injury, CAST/Ei neurons largely retained their mature neuronal profile as determined by single-cell RNA- seq, whereas the C57BL/6 neurons acquired an immature profile. These findings suggest that one facet of the enhanced regenerative phenotype is preservation of neuronal identity in response to injury.Entities:
Keywords: Ascl1; CAST/Ei; RNA sequencing; dorsal root ganglia; miR-7048; regeneration; single-cell analyses
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Year: 2017 PMID: 28768198 PMCID: PMC5565222 DOI: 10.1016/j.celrep.2017.07.010
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423