Zammit, Peter S.; Golding, Jon P.; Nagata, Yosuke; Hudon, Valerie; Partridge, Terence A. and Beauchamp, Jonathan R.
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|DOI (Digital Object Identifier) Link:||https://doi.org/10.1083/jcb.200312007|
|Google Scholar:||Look up in Google Scholar|
Growth, repair, and regeneration of adult skeletal muscle depends on the persistence of satellite cells: muscle stem cells resident beneath the basal lamina that surrounds each myofiber. However, how the satellite cell compartment is maintained is unclear. Here, we use cultured myofibers to model muscle regeneration and show that satellite cells adopt divergent fates. Quiescent satellite cells are synchronously activated to coexpress the transcription factors Pax7 and MyoD. Most then proliferate, down-regulate Pax7, and differentiate. In contrast, other proliferating cells maintain Pax7 but lose MyoD and withdraw from immediate differentiation. These cells are typically located in clusters, together with Pax7-ve progeny destined for differentiation. Some of the Pax7+ve/MyoD-ve cells then leave the cell cycle, thus regaining the quiescent satellite cell phenotype. Significantly, noncycling cells contained within a cluster can be stimulated to proliferate again. These observations suggest that satellite cells either differentiate or switch from terminal myogenesis to maintain the satellite cell pool.
|Item Type:||Journal Article|
|Keywords:||stem; skeletal muscle regeneration; Pax7; MyoD; myogenin|
|Academic Unit/School:||Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences
Faculty of Science, Technology, Engineering and Mathematics (STEM)
|Interdisciplinary Research Centre:||Biomedical Research Network (BRN)|
|Depositing User:||Jon Golding|
|Date Deposited:||28 Jun 2006|
|Last Modified:||10 Feb 2017 05:28|
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