3.8 Article

Transient production of α-smooth muscle actin by skeletal myoblasts during differentiation in culture and following intramuscular implantation

Journal

CELL MOTILITY AND THE CYTOSKELETON
Volume 51, Issue 4, Pages 177-186

Publisher

WILEY-LISS
DOI: 10.1002/cm.10022

Keywords

actin isoforms; myotubes; muscle differentiation; transient myogenic states

Categories

Funding

  1. NCI NIH HHS [CA59717] Funding Source: Medline
  2. NHLBI NIH HHS [HL65572] Funding Source: Medline
  3. NIA NIH HHS [AG09521] Funding Source: Medline
  4. NICHD NIH HHS [HD18179] Funding Source: Medline

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alpha-smooth muscle actin (SMA) is typically not present in post-embryonic skeletal muscle myoblasts or skeletal muscle fibers. However. both primary myoblasts isolated from neonatal mouse muscle tissue, and C2C12. an established myoblast cell line. produced SMA in culture within hours of exposure to differentiation medium. The SMA appeared during the cells' initial elongation, persisted through differentiation and fusion into myotubes, remained abundant in early myotubes, and was occasionally observed in a striated pattern. SMA continued to be present during the initial appearance of sarcomeric actin, but disappeared shortly thereafter leaving only sarcomeric actin in contractile myotubes derived from primary myoblasts. Within one day after implantation of primary myoblasts into mouse skeletal muscle, SMA was observed in the myoblasts; but by 9 days post-implantation. no SMA was detectable in myoblasts or muscle fibers. Thus. both neonatal primary myoblasts and an established myoblast cell line appear to similarly reprise an embryonic developmental program during differentiation in culture as well as differentiation within adult mouse muscles. (C) 2002 Wiley-Liss. Inc.

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