腎と骨代謝 Vol.26 No.2(1)


特集名 サルコペニアと骨代謝
題名 筋細胞分化の分子メカニズム
発刊年月 2013年 04月
著者 内藤 昌志 東京医科歯科大学医歯学総合研究科システム発生・再生医学分野
著者 浅原 弘嗣 東京医科歯科大学医歯学総合研究科システム発生・再生医学分野
【 要旨 】 筋分化を制御するマスター因子であるMyoDの発見以来,さまざまな転写因子を介する筋分化の分子ネットワークは組織分化のモデル系として研究されてきた.筋前駆細胞はPax3/Pax7を発現しているが,筋分化の開始とともにその発現は減少し,basic helix-loop-helixドメインをもつ転写因子であるMyf5,MyoD,Myog,MRF4の発現によって筋芽細胞から筋細胞へと分化して筋管を形成し筋組織となる.これらのbasic helix-loop-helix型の転写因子は互いに重複した機能を有しmuscle regulatory factors(MRF)と呼ばれ,筋分化の中心的な役割を果たす.
Theme Sarcopenia and bone metabolism
Title Molecular mechanism of skeletal muscle differentiation
Author Masashi Naito Department of Systems Biomedicine, Graduate School and Faculty of Medicine, Tokyo Medical and Dental University
Author Hiroshi Asahara Department of Systems Biomedicine, Graduate School and Faculty of Medicine, Tokyo Medical and Dental University
[ Summary ] Muscle differentiation has been studied as a leading model of tissue differentiation since the discovery of MyoD, the master regulator of myogenesis. The fate of myogenic precursor cells is first determined by Pax3/Pax7, the expression of which gradually decreases when myogenesis begins. Alternatively, expression of basic helix-loop-helix transcription factors known as muscle regulatory factors, such as Myf5, MyoD, Myog and MRF4 significantly increases. These cells are specified as myoblasts which fuse together, and differentiate into skeletal muscle fibers. These transcription factors are functionally redundant in part and are form a complex gene network which regulates myogenesis.
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