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MiR-124 inhibits myogenic differentiation of mesenchymal stem cells via targeting Dlx5.
Qadir, Abdul S; Woo, Kyung Mi; Ryoo, Hyun-Mo; Yi, TacGhee; Song, Sun U; Baek, Jeong-Hwa.
  • Qadir AS; Department of Molecular Genetics, School of Dentistry and Dental Research Institute, Seoul National University, Seoul, Korea.
J Cell Biochem ; 115(9): 1572-81, 2014 Sep.
Article en En | MEDLINE | ID: mdl-24733577
MicroRNAs (miRNAs), including miR-1, miR-133, and miR-206, play a crucial role in muscle development by regulating muscle cell proliferation and differentiation. The aim of the present study was to define the effect of miR-124 on myogenic differentiation of mesenchymal stem cells (MSCs). The expression level of miR-124 in skeletal muscles was much lower than those in primary cultured bone marrow-derived MSCs and the bone, fat and brain tissues obtained from C57BL/6 mice. Myogenic stimuli significantly decreased the expression levels of miR-124 in mouse bone marrow-derived MSCs and C2C12 cells. Forced expression of miR-124 suppressed the expression of myogenic marker genes such as Myf5, Myod1, myogenin and myosin heavy chain and multinucleated myotube formation. Blockade of endogenous miR-124 with a hairpin inhibitor enhanced myogenic marker gene expression and myotube formation. During myogenic differentiation of MSCs and C2C12 cells, the levels of Dlx5, a known target of miR-124, were inversely regulated with those of miR-124. Furthermore, overexpression of Dlx5 increased myogenic differentiation, whereas knockdown of Dlx5 using siRNA inhibited myogenesis in C2C12 cells. These results suggest that miR-124 is a negative regulator of myogenic differentiation of MSCs and that upregulation of Dlx5 accompanied with downregulation of miR-124 by myogenic stimuli is necessary for the proper progression of myogenic differentiation.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tibia / Proteínas de Homeodominio / Desarrollo de Músculos / MicroARNs / Fémur / Células Madre Mesenquimatosas Límite: Animals Idioma: En Año: 2014 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Tibia / Proteínas de Homeodominio / Desarrollo de Músculos / MicroARNs / Fémur / Células Madre Mesenquimatosas Límite: Animals Idioma: En Año: 2014 Tipo del documento: Article