首页 | 本学科首页   官方微博 | 高级检索  
     


Critical role of Frizzled1 in age‐related alterations of Wnt/β‐catenin signal in myogenic cells during differentiation
Authors:Ryosuke Doi  Mitsuharu Endo  Kimi Yamakoshi  Yuji Yamanashi  Michiru Nishita  So‐ichiro Fukada  Yasuhiro Minami
Affiliation:1. Department of Physiology and Cell Biology, Graduate School of Medicine, Kobe University, , Kobe, 650‐0017 Japan;2. Department of Mechanism of Aging, Research Institute, National Center for Geriatrics and Gerontology, , Aichi, 474‐8511 Japan;3. Division of Genetics, Department of Cancer Biology, The Institute of Medical Science, The University of Tokyo, , Tokyo, 108‐8639 Japan;4. Laboratory of Molecular and Cellular Physiology, Graduate School of Pharmaceutical Sciences, Osaka University, , Osaka, 565‐0871 Japan
Abstract:
Activation of Wnt/β‐catenin signal in muscle satellite cells (mSCs) of aged mice during myogenic differentiation has been appreciated as an important age‐related feature of the skeletal muscles, resulting in impairment of their regenerative ability following muscle injury. However, it remains elusive about molecules involved in this age‐related alteration of Wnt/β‐catenin signal in myogenic cells. To clarify this issue, we carried out expression analyses of Wnt receptor genes using real‐time RT‐PCR in mSCs isolated from the skeletal muscles of young and aged mice. Here, we show that expression of Frizzled1 (Fzd1) was detected at high levels in mSCs of aged mice. Higher expression levels of Fzd1 were also detected in mSC‐derived myogenic cells from aged mice and associated with activation of Wnt/β‐catenin signal during their myogenic differentiation in vitro. We also provide evidence that suppressed expression of Fzd1 in myogenic cells from aged mice results in a significant increase in myogenic differentiation, and its forced expression in those from young mice results in its drastic inhibition. These findings indicate the critical role of Fzd1 in altered myogenic differentiation associated with aging.
Keywords:
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号