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Hemin enhances differentiation and maturation of cultured regenerated skeletal myotubes.
Funanage, V L; Schroedl, N A; Moses, P A; Smith, S M; Kirwin, J J; Hartzell, C R.
Afiliação
  • Funanage VL; Research Department, Alfred I. duPont Institute, Wilmington, Delaware 19899.
J Cell Physiol ; 141(3): 591-7, 1989 Dec.
Article em En | MEDLINE | ID: mdl-2592428
ABSTRACT
Satellite cells, isolated from marcaine-damaged rat skeletal muscle, differentiate in culture to form contracting, cross-striated myotubes. Addition of 20 microM hemin (ferriprotoporphyrin IX chloride) to the culture medium resulted in increases in the number, size, and alignment of myotubes; in the number of myotubes that exhibited cross-striations; and in the strength and frequency of myotube contractions. Hemin increased satellite cell fusion by 27%, but decreased cell proliferative rate by 30%. Hemin increased the specific activity of creatine kinase (CK), a sensitive indicator of muscle differentiation, by 157%. Separation of CK isoenzymes by agarose gel electrophoresis showed that hemin increased only the muscle-specific CK isoenzymes (MM-CK and MB-CK). Thus, hemin seems to duplicate some of the effects of innervation on cultured myotubes by increasing contraction frequency and strength, appearance of cross-striations, and muscle-specific isoenzymes. In contrast, 3-amino-1,2,4-triazole, an inhibitor of heme biosynthesis, decreased the number of cross-striated myotubes, the strength and frequency of myotube contractions, and CK activity. These inhibitory effects were reversed by hemin. Collectively, these results demonstrate a physiologically significant role for heme in myotube maturation.
Assuntos
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Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regeneração / Heme / Hemina / Músculos Limite: Animals Idioma: En Revista: J Cell Physiol Ano de publicação: 1989 Tipo de documento: Article
Buscar no Google
Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Regeneração / Heme / Hemina / Músculos Limite: Animals Idioma: En Revista: J Cell Physiol Ano de publicação: 1989 Tipo de documento: Article