Your browser doesn't support javascript.
loading
AP-1cFos/JunB/miR-200a regulate the pro-regenerative glial cell response during axolotl spinal cord regeneration.
Sabin, Keith Z; Jiang, Peng; Gearhart, Micah D; Stewart, Ron; Echeverri, Karen.
Afiliação
  • Sabin KZ; Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN, 55455, USA.
  • Jiang P; Marine Biological Laboratory, Eugene Bell Center for Regenerative Biology and Tissue Engineering, Woods Hole, 02543, MA, USA.
  • Gearhart MD; Morgridge Institute for Research, Madison, 53715, WI, USA.
  • Stewart R; Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN, 55455, USA.
  • Echeverri K; Morgridge Institute for Research, Madison, 53715, WI, USA.
Commun Biol ; 2: 91, 2019.
Article em En | MEDLINE | ID: mdl-30854483
ABSTRACT
Salamanders have the remarkable ability to functionally regenerate after spinal cord transection. In response to injury, GFAP+ glial cells in the axolotl spinal cord proliferate and migrate to replace the missing neural tube and create a permissive environment for axon regeneration. Molecular pathways that regulate the pro-regenerative axolotl glial cell response are poorly understood. Here we show axolotl glial cells up-regulate AP-1cFos/JunB after injury, which promotes a pro-regenerative glial cell response. Injury induced upregulation of miR-200a in glial cells supresses c-Jun expression in these cells. Inhibition of miR-200a during regeneration causes defects in axonal regrowth and transcriptomic analysis revealed that miR-200a inhibition leads to differential regulation of genes involved with reactive gliosis, the glial scar, extracellular matrix remodeling and axon guidance. This work identifies a unique role for miR-200a in inhibiting reactive gliosis in axolotl glial cells during spinal cord regeneration.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Axônios / Regulação da Expressão Gênica / Neuroglia / Fator de Transcrição AP-1 / MicroRNAs / Regeneração da Medula Espinal Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Axônios / Regulação da Expressão Gênica / Neuroglia / Fator de Transcrição AP-1 / MicroRNAs / Regeneração da Medula Espinal Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article