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Presence of embryonic myosin in normal postural muscles of the adult rat

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Abstract

Indirect immunofluorescence was used to localize embryonic myosin heavy chains in soleus, adductor longus, tibialis anterior, plantaris, and extensor digitorum longus muscles of 6-month-old rats. A monoclonal antibody (2B6), specifically recognizing rat embryonic myosin, was applied to unfixed, transverse, frozen sections. The number of embryonic myosin-positive (EMP) extrafusal fibers was expressed as a percentage of the total number of fibers. EMP extrafusal fibers were only seen in the soleus and adductor longus muscles, both postural muscles. Approximately 1% of the soleus muscle fibers appeared positively stained for embryonic myosin. The majority of such fibers had a small diameter (<500 ν), appeared intensely fluorescent, and typically contained central nuclei. Re-expression of embryonic myosin due to spontaneous fiber denervation is not a likely factor in this study, since alpha-bungarotoxin and N-CAM localization were restricted to the motor end-plate region of EMP fibers. Since embryonic myosin was shown to disappear in all normal-sized myofibers by 2 to 3 months of age, the results suggest that the EMP extrafusal fibers seen in postural muscles of 6 to 12-month-old animals are regenerating myofibers. We speculate that a small number of muscle fibers may be regenerating in normal, adult postural muscles, in response to fiber damage possibly caused by excessive recruitment or overloading.

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References

  • Butler-Browne GS, Whalen RG (1984) Myosin isozyme transitions occurring during the postnatal development of the rat soleus muscle Dev Biol 102:324–334

    Google Scholar 

  • Butler-Browne GS, Eriksson PO, Laurent C, Thornell LE (1988) Adult human masseter muscle fibers express myosin isozymes characteristic of development. Muscle Nerve 11:610–620

    Google Scholar 

  • Cardasis CA, Padykula HA (1981) Ultrastructural evidence indicating reorganization at the neuromuscular junction in the normal rat soleus muscle. Anat Rec 200:41–59

    Google Scholar 

  • Cerny L, Bandman E (1987) Expression of myosin heavy chain isoforms in regenerating myotubes of innervated and denervated chicken pectoralis muscle. Dev Biol 119:360–362

    Google Scholar 

  • d'Albis A, Couteaux R, Janmot C, Roulet A (1989a) Specific programs of myosin expression in the postnatal development of rat muscle. Eur J Biochem 183:583–590

    Google Scholar 

  • d'Albis A, Couteaux R, Janmot C, Mira JC (1989b) Myosin isoform transitions in regeneration of fast and slow muscles during postnatal development of the rat. Dev Biol 135:320–325

    Google Scholar 

  • Gambke B, Rubinstein NA (1984) A monoclonal antibody to the embryonic myosin heavy chain of rat skeletal muscle. J Biol Chem 259:12092–12100

    Google Scholar 

  • Giddings CJ, Neaves WB, Gonyea WJ (1985) Muscle fiber necrosis and regeneration induced by prolonged weight-lifting exercise in the cat. Anat Rec 211:133–141

    Google Scholar 

  • Gorza L, Sartore S, Triban C, Schiaffino S (1983) Embryonic-like myosin heavy chains in regenerating chicken muscle. Exp Cell Res 143:395–403

    Google Scholar 

  • Granger BL, Lazarides E (1979) Desmin and vimentin co-exist at the periphery of the myofibril Z disc. Cell 18:1053–1063

    Google Scholar 

  • Jakubiec-Puka A, Kordewska J, Catani C, Carraro U (1990) Myosin heavy chain isoform composition in striated muscle after denervation and self-reinnervation. Eur J Biochem 193:623–628

    Google Scholar 

  • Kirschbaum B, Schneider S, Izumo S, Mahdavi V, Nadal-Ginard B, Pette D (1990) Rapid and reversible changes in myosin heavy chain expression in response to increased neuromuscular activity of rat fast twitch muscle. FEBS Lett 268:75–78

    Google Scholar 

  • LaFramboise W, Daood M, Guthrie R, Butler-Browne G, Whalen R, Ontell M (1990) Myosin isoforms in neonatal rat extensor digitorum longus, diaphragm, and soleus muscles. Am J Physiol 259:L116-L122

    Google Scholar 

  • Lexell J, Jarvis J, Downham D, Salmons S (1993) Stimulation-induced damage in rabbit fast-twitch skeletal muscles: a quantitative morphological study of the influence of pattern and frequency. Cell Tissue Res 273:357–362

    Google Scholar 

  • Maier A, Gambke B, Pette D (1986) Degeneration-regeneration as a mechanism contributing to the fast to slow conversion of chronically stimulated fast-twitch rabbit muscle. Cell Tissue Res 244:635–643

    Google Scholar 

  • Maier A, Gambke B, Pette D (1988) Immunohistochemical demonstration of embryonic myosin heavy chains in adult mammalian intrafusal fibers. Histochemistry 88:267–271

    Google Scholar 

  • McCormick KM, Schultz E (1992) Mechanisms of nascent fiber formation during avian skeletal muscle hypertrophy. Dev Biol 150:319–334

    Google Scholar 

  • McCormick K, Schultz E (1994) Role of satellite cells in altering myosin expression during avian skeletal muscle hypertrophy. Dev Dynam 199:52–63

    Google Scholar 

  • Pette D, Vrbova G (1985) Neural control of phenotypic expression in mammalian muscle fibers. Muscle Nerve 8:676–689

    Google Scholar 

  • Sanes J, Schachner M, Covault J (1986) Expression of several adhesive macromolecules (N-CAM, L1, J1, NILE, Uvomorulin, Laminin, Fibronectin, and a Heparin Sulfate Proteoglycan) in embryonic, adult, and denervated adult skeletal muscle. J Cell Biol 102:420–431

    Google Scholar 

  • Sartore S, Gorza L, Schiaffino S (1982) Fetal myosin heavy chains in regenerating muscle. Nature 298:294–296

    Google Scholar 

  • Schiaffino S, Gorza L, Pitton G, Saggin L, Ausoni S, Sartore S, Lomo T (1988) Embryological and neonatal myosin heavy chains in denervated and paralyzed rat skeletal muscle. Dev Biol 127:1–11

    Google Scholar 

  • Soussi-Yanicostas N, Barbet J, Laurent-Winter C, Barton P, Butler-Browne G (1990) Transition of myosin isozymes during development of human masseter muscle. Development 108:239–249

    Google Scholar 

  • Whalen R, Sell S, Butler-Browne G, Schwartz K, Bouveret P, Pinset-Harstrom I (1981) Three myosin heavy chain isozymes appear sequentially in rat muscle development. Nature 292:805–809

    Google Scholar 

  • Wieczorek D, Periasamy M, Butler-Browne G, Whalen R, Nadal-Ginard B (1985) Co-expression of multiple myosin heavy chain genes, in addition to a tissue-specific one, in extraocular musculature. J Cell Biol 101:618–629

    Google Scholar 

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Wanek, L.J., Snow, M.H. Presence of embryonic myosin in normal postural muscles of the adult rat. Cell Tissue Res 280, 541–548 (1995). https://doi.org/10.1007/BF00318358

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