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New method for the accurate characterization of single human skeletal muscle fibres demonstrates a relation between mATPase and MyHC expression in pure and hybrid fibre types

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Summary

In the present study we have developed a method which, by combining histochemical, immunohistochemical, electrophoretic and immunoblotting analyses on a single fibre, enables a sensitive characterization of human skeletal muscle fibres dissected from freeze-dried biopsy samples. For histochemical (and immunohistochemical) analysis fibre fragments (500 μm) of individual fibres were mounted in an embedding medium to allow cryostat sections of normalized thickness to be reproducibly obtained. The specificity of the myofibrillar Ca2+ ATPase (mATPase) staining profiles in gelatin-embedded single fibre sections was tested by immunohistochemical reactions with anti-myosin heavy chain (MyHC) monoclonal antibodies specific to human MyHC I, IIA, IIB and IIA+IIB and by gel electrophoresis.

The combined methodologies demonstrated the specificity of the mATPase staining patterns which correlated to the expression of distinct MyHC isoforms. In addition the results provide evidence that many fibres co-expressed different MyHC isoforms in variable relative amounts, forming a continuum. Staining intensities for mATPase, converted into optical density values by image analysis revealed that a relationship between mATPase and MyHC expression holds for hybrid fibres even when displaying one MyHC type with overwhelming dominance. The results also revealed that three MyHC isoforms I, IIA and IIB can be co-expressed on a single muscle fibre. In such a case mATPase alone, with the current protocols, does not allow an accurate characterization of the specific MyHC-based fibre type(s). although some hybrid fibres may have displayed a non-uniform expression of myosins along their lengths, most fibres from the IIA/B group (type) remained very stable with respect to the relative amounts of the MyHCs expressed. Finally, a second slow MyHC isoform was recognized on immunoblots of a mixed muscle sample.

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References

  • BARANY, M. J. (1967) ATPase activity of myosin correlated with speed of muscle shortening. Gen. Physiol. 50, 197–218.

    Google Scholar 

  • BERGSTROM, J. (1962) Muscle electrolytes in man. Scand. J. Clin. Lab. Invest. 14, suppl. 68.

    Google Scholar 

  • BILLETER, R., WEBER, H. & LUTZ, H. (1980) Myosin types in human skeletal muscle fibres. Histochem. 65, 249–59.

    Google Scholar 

  • BIRAL, D., BETTO, R., DANIELI-BETTO & SALVIATI, G. (1988) Myosin heavy chain composition of single fibres from normal human muscle. Biochem. J. 250, 307–8.

    Google Scholar 

  • BOTTINELLI, R., BETTO, R., SCHIAFFINO, S. & REGGIANI, C. (1994) Unloaded shortening velocity and myosin heavy chain and alkali light chain isoform composition in rat skeletal muscle fibres. J. Physiol. 478, 341–9.

    Google Scholar 

  • BREDMAN, J. J. (1991) Functional heterogeneity of the Masseter muscle: a histochemical study. Academisch Proefschipft (PhD Thesis). University of Amsterdam.

  • BREDMAN, J. J., WEIJS, W. A. & MOORMAN, A. F. M. (1992) Presence of cardiac a-myosin correlates with histochemical myosin Ca2+ ATPase activity in rabbit masseter muscle. Histochem. J. 24, 260–5.

    Google Scholar 

  • BROOKE, M. H. & KAISER, K. K. (1970) Muscle fibre types: how many and what kind? Arch. Neurol. 23, 369–79.

    Google Scholar 

  • BUTCHER, R. G. (1971) The chemical determination of section thickness. Histochemie 28, 131–6.

    Google Scholar 

  • CHRISTENSEN, L. & STRANGE, L. (1987) Universal immuno-peroxidase staining protocol to optimize the use of polyclonal and monoclonal antibodies. J. Histotechnol. 10, 11–15.

    Google Scholar 

  • DONALDSSON, S. K. B. (1984) Ca2+-activated force-generating properties of mammalian skeletal muscle fibres: histochemically identified single peeled rabbit fibres. J. Muscle Res. Cell Motil. 5, 593–612.

    Google Scholar 

  • EDDINGER, T. J. & MOSS, R. L. (1987) Mechanical properties of skinned single fibres of identified types from rat diaphagm. Am. J. Physiol. 253, C210–18.

    Google Scholar 

  • ESSEN, B., JANSSON, E. HENRIKSSON, J., TAYLOR, A. W. & SALTIN, B. (1975) Metabolic characteritics of fibre types in human skeletal muscle. Acta Physiol. Scand. 95, 153–65.

    Google Scholar 

  • FAZEKAS DE ST. GROTH, S. & SCHEIDEGGER, D. (1980) Production of monoclonal antibodies: strategy and tactics. J. Immunol. Methods 35, 1–21.

    Google Scholar 

  • GOLDSPINK, G., SCUTT, A., MARTINDALE, J., JAENICKE, T., TURAY, L. & GERLACH, G.-F. (1991) Stretch and force generation induce rapid hypertrophy and isoform gene switching in adult skeletal muscle. Biochem. Trans. 19, 368–73.

    Google Scholar 

  • GOLDSPINK, G., SCUTT, A., LOUGHNA, P. T., WELLS, D. J., JEANICKE, T. & GERLACH, G. F. (1992) Gene expression in skeletal muscle in response to stretch and force generation. Am. J. Physiol. 262, R356–63.

    Google Scholar 

  • GREASER, M. L., MOSS, R. L. & REISER, P. J. (1988) Variation in contractile properties of rabbit single muscle fibres in relation to troponin isoforms and myosin light chains. J. Physiol. 406, 85–98.

    Google Scholar 

  • GUTH, L. & SAMAHA, F. J. (1969) Procedure for the histochemical demonstration of actomyosin ATPase. Exp. Neurol. 28, 365–6.

    Google Scholar 

  • HAWKES, R., NIDAY, E. & GORDON, J. (1982) A dot-immunoblotting assay for monoclonal and other antibodies. Anal. Biochem. 119, 142–7.

    Google Scholar 

  • HOH, J. F. Y., MCGRATH, P. A. & WHITE, R. J. (1976) Electrophoretic analysis of multiple forms of myosin in fast-twitch and slow-twitch muscle in the chick. Biochem. J. 157, 87–95.

    Google Scholar 

  • HUGHES, S. M., CHO, M., KARSCH-MIZRACHI, I., TRAVIS, M., SILBERSTEIN, L., LEINWAND, L. A. & BLAU, H. M. (1993) Three myosin heavy chains sequentially expressed in developing mammalian skeletal muscle. Develop. Biol. 158, 183–99.

    Google Scholar 

  • JANDRESKI, M. A., SOLE, M. J. & LIEW, C.-C. (1987) Two different forms of beta myosin heavy chain are expressed in human striated muscle. Hum. Genet. 77, 127–31.

    Google Scholar 

  • JONKER, A., GEERTS, W. J. C., CHARLES, R., LAMERS, W. H. & VAN NOORDEN, C. J. F. (1995) Image analysis and image processing as a tool to measure initial rates of enzyme reactions throughout the liver lobule with glutamate dehydrogenase as a model system. J. Histochem. Cytochem., in press.

  • KLITGAARD, H., ZHOU, M. & RICHTER, E. A. (1990) Myosin heavy chain composition of single fibres from m. biceps brachii of male body builders. Acta Physiol. Scand. 140, 175–80.

    Google Scholar 

  • LAEMMLI, U. K. (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227, 680–5.

    Google Scholar 

  • LANNERGREN, J. (1987) Contractile properties and myosin isoenzymes of various kinds of Xenopus twitch muscle fibres. J. Muscle Res. Cell Motil. 8, 260–73.

    Google Scholar 

  • LARSSON, L. & MOSS, R. L. (1993) Maximum velocity of shortening in relation to myosin isoform composition in single fibres from human skeletal muscles. J. Physiol. 472, 595–614.

    Google Scholar 

  • LIND, A. & KERNELL, D. (1991) Myofibrillar ATPase histochemistry of rat skeletal muscles: a “two-dimensional” quantitative approach. J. Histochem. Cytochem. 39, 589–97.

    Google Scholar 

  • MOORMAN, A. F. M., BOERDE, P. A. J., LINDERS, M. TH. & CHARLES, R. (1984) The histone H5 variant in Xenopus leavis. Cell Differ. 14, 113–23.

    Google Scholar 

  • OAKLEY, B. R., KIRSCH, D. R. & MORRIS, N. R. (1980) A simplified ultrasensitive silver stain for detecting proteins in polyacrylamide gels. Anal. Biochem. 105, 361–3.

    Google Scholar 

  • PAVLATH, G. K., RICH, K., WEBSTER, S. G. & BLAU, H. M. (1989) Localization of muscle gene products in nuclear domains. Nature 337, 570–3.

    Google Scholar 

  • REISER, P. J., MOSS, R. L., GIULIAN, G. G. & GREASER, M. L. (1985) Shortening velocity in single fibres from adult rabbit soleus muscles is correlated with myosin heavy chain composition. J. Biol. Chem. 260, 9077–80.

    Google Scholar 

  • REISER, P. J., GREASER, M. L. & MOSS, R. L. (1988) Myosin heavy chain composition of single cells from avian slow skeletal muscle is strongly correlated with velocity of shortening during development. Dev. Biol. 129, 400–7.

    Google Scholar 

  • ROME, L. C. (1993) The design of the muscular system. In Neuromuscular Fatigue (edited by SARGEANT, A. J. & KERNELL, D.) pp. 129–136. Academy Series, Royal Netherlands Academy of Arts and Sciences. Amsterdam: Elsevier-North Holland.

    Google Scholar 

  • ROME, L. C., SOSNICKI, A. A. & NOBLE, D. (1990) Maximum velocity of shortening of three fibre types from horse muscle: implications for scaling with body size. J. Physiol. 431, 173–85.

    Google Scholar 

  • SALVIATI, G., BIASIA, E. & ALOISI, M. (1986) Synthesis of fast myosin induced by fast ectopic innervation of rat soleus muscle is restricted to the ectopic endplate region. Nature 332, 637–9.

    Google Scholar 

  • SANT' ANA PEREIRA, J. A. A. & MOORMAN, A. F. M. (1994) Do type IIB fibres of humans correspond to the IIX/D or to the IIB of rats? J. Physiol. 479, 161–2P (abstract).

    Google Scholar 

  • STARON, R. S. (1991) Correlation between myofibrillar ATPase activity and myosin heavy chain composition in single human muscle fibres. Histochem. 96, 21–4.

    Google Scholar 

  • STARON, R. C. & PETTE, D. (1986) Correlation between myofibrillar ATPase activity and myosin heavy chain composition in rabbit muscle fibres. Histochem. 86, 19–23.

    Google Scholar 

  • STARON, R. C. & PETTER, D. (1987) Nonuniform myosin expression along single fibres of chronically stimulated and contralateral rabbit tibialis anterior muscles. Pflügers Arch. 409, 67–73.

    Google Scholar 

  • STARON, R. C. & PETTE, D. (1993) The continuum of pure and hybrid myosin heavy chain-based fibre types in rat skeletal muscle. Histochem. 100, 149–53.

    Google Scholar 

  • TAKEKURA, H. & YOSHIOKA, T. (1987) Determination of metabolic profiles on single muscle fibres of different types. J. Muscle Res. Cell Motil. 8, 342–8.

    Google Scholar 

  • TAYLOR, L. D. & BANDMAN, E. (1989) Distribution of fast myosin heavy chain isoform in thick filaments of developing chicken pectoral muscle. J. Cell Biol. 108, 533–42.

    Google Scholar 

  • VAN DERLAARSE, W. J., DIEGENBACH, P. C. & HEMMINGA, M. A. (1986) Calcium-stimulated myofibrillar ATPase activity correlates with shorteing velocity of muscle fibres of Xenopus laevis. Histochem. J. 18, 487–96.

    Google Scholar 

  • VAN DERLAARSE, W. J., DIEGENBACH, P. C. & ELZINGA, G. (1989) Maximum rate of oxygen consumption and quantitative histochemistry of succinate dehydrogenase in single muscle fibres of Xenopus laevis. J. Muscle Res. Cell Motil. 10, 221–8.

    Google Scholar 

  • VØLLESTAD, N. K., VAAGE, O. & HERMANSEN, L. (1984) Muscle glycogen depletion patterns in type I and subgroups of type II fibres during prolonged severe exercise in man. Acta Physiol. Scand. 122, 433–41.

    Google Scholar 

  • WESSELS, A., VERMEULEN, J. L. M., VIRAGH, Sz., KÁLMÁN, F., LAMERS, W. H. & MOORMAN, A. F. M. (1991) Spatial distribution of “tissue specific” antigens in the developing human heart and skeletal muscle. II. An immunohistochemical analysis of myosin heavy chain iso-from expression patterns in the embryonic heart. Anat. Rec. 229, 355–68.

    Google Scholar 

  • WILLIAMS, P. E., WATT, P., BICIK, V. & GOLDSPINK, G. (1986) Effect of stretch combined with electrical stimulation on the type of sarcomeres produced at the ends of muscle fibres. Exp. Neurol. 93, 500–9.

    Google Scholar 

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Pereira, J.A.A.S.A., Wessels, A., Nijtmans, L. et al. New method for the accurate characterization of single human skeletal muscle fibres demonstrates a relation between mATPase and MyHC expression in pure and hybrid fibre types. J Muscle Res Cell Motil 16, 21–34 (1995). https://doi.org/10.1007/BF00125307

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