4.8 Article

Biological progression from adult bone marrow to mononucleate muscle stem cell to multinucleate muscle fiber in response to injury

Journal

CELL
Volume 111, Issue 4, Pages 589-601

Publisher

CELL PRESS
DOI: 10.1016/S0092-8674(02)01078-4

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Funding

  1. NHLBI NIH HHS [HL65572] Funding Source: Medline
  2. NIA NIH HHS [AG00259, AG20961, AG09521] Funding Source: Medline
  3. NICHD NIH HHS [HD18179] Funding Source: Medline

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Adult bone marrow-derived cells (BMDC) are shown to contribute to muscle tissue in a step-wise biological progression. Following irradiation-induced damage, transplanted GFP-labeled BMDC become satellite cells: membrane-ensheathed mononucleate muscle stem cells. Following a subsequent exercise-induced damage, GFP-labeled multinucleate myofibers are detected. Isolated GFP-labeled satellite cells are heritably myogenic. They express three characteristic muscle markers, are karyotypically diploid, and form clones that can fuse into multinucleate cells in culture or into myofibers; after injection into mouse muscles. These results suggest that two temporally distinct injury-related signals first induce BMDC to occupy the muscle stem cell niche and then to help regenerate mature muscle fibers. The stress-induced progression of BMDC to muscle satellite cell to muscle fiber results in a contribution to as many as 3.5% of muscle fibers and is due to developmental plasticity in response to environmental cues.

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