Pax3 and Pax7 have distinct and overlapping functions in adult muscle progenitor cells

Author:

Relaix Frédéric1,Montarras Didier1,Zaffran Stéphane1,Gayraud-Morel Barbara2,Rocancourt Didier1,Tajbakhsh Shahragim2,Mansouri Ahmed3,Cumano Ana4,Buckingham Margaret1

Affiliation:

1. Unité de Génétique Moléculaire du Développement, Centre National de la Recherche Scientifique URA 2578, Département de Biologie du Développement

2. Groupe de Cellules Souches et Développement, Centre National de la Recherche Scientifique URA 2578, Département de Biologie du Développement

3. Department of Molecular Cell Biology, Max-Planck Institute for Biophysical Chemistry, D-37077 Gottingen, Germany

4. Unite de Biologie Moleculaire du Gene, Département d'Immunologie, Institut National de la Santé et de la Recherche Medicale U277, Institut Pasteur, 75724 Paris Cedex 15, France

Abstract

The growth and repair of skeletal muscle after birth depends on satellite cells that are characterized by the expression of Pax7. We show that Pax3, the paralogue of Pax7, is also present in both quiescent and activated satellite cells in many skeletal muscles. Dominant-negative forms of both Pax3 and -7 repress MyoD, but do not interfere with the expression of the other myogenic determination factor, Myf5, which, together with Pax3/7, regulates the myogenic differentiation of these cells. In Pax7 mutants, satellite cells are progressively lost in both Pax3-expressing and -nonexpressing muscles. We show that this is caused by satellite cell death, with effects on the cell cycle. Manipulation of the dominant-negative forms of these factors in satellite cell cultures demonstrates that Pax3 cannot replace the antiapoptotic function of Pax7. These findings underline the importance of cell survival in controlling the stem cell populations of adult tissues and demonstrate a role for upstream factors in this context.

Publisher

Rockefeller University Press

Subject

Cell Biology

Cited by 558 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3