Somatic stem cells cycle slowly or remain quiescent until required for tissue repair and maintenance. Upon muscle injury, stem cells that lie between the muscle fiber and basal lamina (satellite cells) are activated, proliferate, and eventually differentiate to repair the damaged muscle. Satellite cells in healthy muscle are quiescent, do not express MyoD family transcription factors or cell cycle regulatory genes and are insulated from the surrounding environment. Here, we report that the p38α/β family of mitogen-activated protein kinases (MAPKs) reversibly regulates the quiescent state of the skeletal muscle satellite cell. Inhibition of p38α/β MAPKs (a) promotes exit from the cell cycle, (b) prevents differentiation, and (c) insulates the cell from most external stimuli allowing the satellite cell to maintain a quiescent state. Activation of satellite cells and p38α/β MAPKs occurs concomitantly, providing further support that these MAPKs function as a molecular switch for satellite cell activation.
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11 April 2005
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April 11 2005
The p38α/β MAPK functions as a molecular switch to activate the quiescent satellite cell
Nathan C. Jones,
Nathan C. Jones
1Bayer Corporation, Research Triangle Park, NC 27709
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Kristina J. Tyner,
Kristina J. Tyner
3Department of Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309
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Lisa Nibarger,
Lisa Nibarger
3Department of Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309
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Heather M. Stanley,
Heather M. Stanley
3Department of Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309
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Dawn D.W. Cornelison,
Dawn D.W. Cornelison
3Department of Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309
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Yuri V. Fedorov,
Yuri V. Fedorov
2Dharmacon Research, Lafayette, CO 80026
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Bradley B. Olwin
Bradley B. Olwin
3Department of Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309
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Nathan C. Jones
1Bayer Corporation, Research Triangle Park, NC 27709
Kristina J. Tyner
3Department of Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309
Lisa Nibarger
3Department of Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309
Heather M. Stanley
3Department of Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309
Dawn D.W. Cornelison
3Department of Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309
Yuri V. Fedorov
2Dharmacon Research, Lafayette, CO 80026
Bradley B. Olwin
3Department of Molecular, Cellular, and Developmental Biology, University of Colorado at Boulder, Boulder, CO 80309
Correspondence to Bradley B. Olwin: [email protected]
N.C. Jones and K.J. Tyner contributed equally to this work.
Abbreviation used in this paper: ERK, extracellular signal-regulated kinase.
Received:
August 11 2004
Accepted:
February 25 2005
Online ISSN: 1540-8140
Print ISSN: 0021-9525
The Rockefeller University Press
2005
J Cell Biol (2005) 169 (1): 105–116.
Article history
Received:
August 11 2004
Accepted:
February 25 2005
Citation
Nathan C. Jones, Kristina J. Tyner, Lisa Nibarger, Heather M. Stanley, Dawn D.W. Cornelison, Yuri V. Fedorov, Bradley B. Olwin; The p38α/β MAPK functions as a molecular switch to activate the quiescent satellite cell . J Cell Biol 11 April 2005; 169 (1): 105–116. doi: https://doi.org/10.1083/jcb.200408066
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