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Research Article| Volume 11, ISSUE 5, P425-444, November 1970

Regeneration of muscle in Duchenne muscular dystrophy: An electron microscope study

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      Abstract

      Electron-microscopic observations have been made on skeletal muscle from cases of Duchenne muscular dystrophy and particular attention has been paid to the regenerative changes. The degenerative changes encountered were similar to those which have been found by previous workers. The most basic change was a segmental one and consisted of supercontraction of myofibrils which appeared to precede their fusion and subsequent breakdown. It is suggested that the supercontraction may represent a state of contracture or failure of relaxation due to a relative deficiency of ATP in the muscle fibre.
      Regenerative changes were found in considerable numbers of muscle fibres particularly in the younger cases. In fibres showing advanced degenerative changes, “satellite cells” were commonly found to be enlarged and to have a more elaborate organelle content than that of the resting “satellite cell”. Thin filaments were found in the cytoplasm of some “satellite cells” confirming their ability to differentiate into myoblasts. Ribosomal aggregates were found within the degenerate sarcoplasm of some fibres but were not associated with new filament formation.
      Regenerating fibres were recognized by the presence of polyribosomes in the sarcoplasm and large nuclei with dispersed chromatin and prominent nucleoli. Although in some fibres the pattern of myofibrillar development appeared to be quite normal, in many regenerating fibres the myofibrils were poorly aligned and at times completely disorganized and often showed abnormalities such as streaming of the Z-band or other focal deficiencies in isolated sarcomeres. Mitochondria were sparse in the vicinity of developing myofibrils. In some small fibres which ended blindly, regenerative changes appeared to have become arrested.
      The present observations indicate that although dystrophic muscle is capable of regeneration, the pattern of morphological development of the contractile elements in regenerating fibres is often abnormal. Moreover, there is evidence of metabolic abnormalities in such fibres. The observed abnormalities in the regeneration of dystrophic muscle correlate with the known abnormal growth pattern of dystrophic muscle in tissue culture. The possible reasons for these abnormalities are considered.
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      References

      1. Allbrook, D. B. (1968) Personal communication.

        • Bergman R.A.
        Myogenesis in rat embryos.
        Bull. Johns Hopk. Hosp. 1962; 110: 187-201
        • Bonetti E.
        • Toschi F.N.
        • Levi M.
        Le frazioni del fosforo acido-solubile nella distrofia muscolare progressiva.
        Sperimentale. 1954; 104 (Fasc. xi-xii): 315
        • Church J.C.T.
        The Satellite Cell of Skeletal Muscle.
        in: M.D. Thesis. Cambridge University, Cambridge1968
        • Church J.C.T.
        • Noronha R.F.X.
        • Allbrook D.B.
        Satellite cells and skeletal muscle regeneration.
        Brit. J. Surg. 1966; 53: 638-642
        • Gilbert R.K.
        • Hazard J.B.
        Regeneration in human skeletal muscle.
        J. Path. Bact. 1965; 89: 503-512
        • Goldspink G.
        Succinic dehydrogenase content of individual muscle fibres at different ages and stages of growth.
        Life Sci. 1969; 8: 791-808
        • Heywood S.M.
        • Rich A.
        In vitro synthesis of native myosin, actin and tropomyosin from embryonic chick polyribosomes.
        in: Proc. nat. Acad. Sci. (Wash.). 59. 1968: 590-597
        • Hudgson P.
        • Research Committee of the Muscular Dystrophy Group
        Ultrastructural changes in dystrophic muscle.
        in: Research in Muscular Dystrophy. Proceedings of the 4th Symposium. Pitman, London1968: 207-222
      2. Hudgson, P. (1969). Personal communication.

        • Hudgson P.
        • Pearce G.W.
        • Walton J.N.
        Pre-clinical muscular dystrophy: Histopathological changes observed on muscle biopsy.
        Brain. 1967; 90: 565-576
        • Kakulas B.A.
        • Adams R.D.
        Principles of myopathology as illustrated in the nutritional myopathy of the Rottnest quokka (Setonix brachyurus).
        Ann. N.Y. Acad. Sci. 1966; 138: 90-101
        • Kakulas B.A.
        • Papadimitriou J.M.
        • Knight J.
        • Mastaglia F.L.
        Normal and abnormal human muscle in tissue culture.
        in: Proc. Aust. Ass. Neurol.5. 1968: 79-85
        • Larson P.F.
        • Hudgson P.
        • Walton J.N.
        Morphological relationship of polyribosomes and myosin filaments in developing and regenerating skeletal muscle.
        Nature (Lond.). 1969; 222: 1168-1169
        • Larson P.F.
        • Jenkison M.
        • Hudgson P.
        The morphological development of chick embryo skeletal muscle grown in tissue culture as studied by electron microscopy.
        J. neurol. Sci. 1970; 10: 385-405
        • Larson P.F.
        • Fulthorpe J.J.
        • Walton J.N.
        Muscle regeneration in normal mice.
        in: An electron microscope study. 1970 (In preparation)
        • Lechner K.
        • Moser K.
        • Stockinger L.
        Biochemische und elektronenoptische Untersuchungen bei einem Fall von idiopathischer paroxysmaler Myoglobinurie.
        Beitr. path. Anat. 1966; 134: 65-83
      3. Mastaglia, F. L. (1969) Unpublished observations.

        • Mastaglia F.L.
        • Kakulas B.A.
        A histological and histochemical study of skeletal muscle regeneration in polymyositis.
        J. neurol. Sci. 1970; 10: 471-487
        • Mastaglia F.L.
        • Walton J.N.
        An electron microscope study of skeletal muscle in polymyositis.
        1970 (In preparation)
        • Mastaglia F.L.
        • Kakulas B.A.
        Regeneration in Duchenne muscular dystrophy: A histological and histochemical study.
        Brain. 1970; 92: 809-818
        • Mastaglia F.L.
        • Papadimitriou J.M.
        • Kakulas B.A.
        Restricted forms of muscular dystrophy.
        in: A study of 11 cases. Proc. Aust. Ass. Neurol.6. 1969: 107-121
        • Mauro A.
        Satellite cells of skeletal muscle fibres.
        J. biophys. biochem. Cytol. 1961; 9: 493-495
        • Milhorat A.T.
        • Shafiq S.A.
        • Goldstone L.
        Changes in muscle structure in dystrophic patients, carriers and normal siblings seen by electron microscopy; correlation with levels of serum creatine phosphokinase (CPK).
        Ann. N.Y. Acad. Sci. 1966; 138: 246-292
        • Mölbert E.
        Das elektronenmikroskopische Bild des Skelettmuskels bei Dystrophia musculorum progressiva Erb.
        Naturwissenschaften. 1960; 47: 186-187
        • McArdle B.
        Speculations arising from certain biochemical and morphological alterations in muscle disease.
        in: Milhorat A.T. Proceedings of an International Scientific Conference convened by the Muscular Dystrophy Associations of America, Arden House, Harriman, N.Y., 22–27 October, 1966Exploratory Concepts in Muscular Dystrophy and Related Disorders. Excerpta Medica, Amsterdam1967: 334-340 (1967)
        • McArdle B.
        Regeneration in neuromuscular disorders.
        in: Proc. of the International Congress on Muscle Diseases, Milan, 1969 Excerpta Medica Foundation, Amsterdam1969 (International Congress Series No. 186)
        • McComas A.J.
        • Mrozek K.
        Denervated muscle fibres in hereditary mouse dystrophy.
        J. Neurol. Neurosurg. Psychiat. 1967; 30: 526-530
        • Ogawa Y.
        Synthesis of skeletal muscle proteins in early embryos and regenerating tissue of chick and Triturus.
        Exp. Cell Res. 1962; 26: 269-277
        • Pearce G.W.
        Tissue culture and electron microscopy in muscle disease.
        in: Walton J.N. Disorders of Voluntary Muscle. Churchill, London1964
        • Pearce G.W.
        Electron microscopy in the study of muscular dystrophy.
        Ann. N.Y. Acad. Sci. 1966; 138: 138-150
        • Pearson C.M.
        Histopathological features of muscle in the preclinical stages of muscular dystrophy.
        Brain. 1962; 85: 109-120
        • Price H.M.
        • Howes E.L.
        • Blumberg J.M.
        Ultrastructural alterations in skeletal muscle fibres injured by cold.
        Lab. Invest. 1964; 13: 1279-1302
        • Reznik M.
        Origin of myoblasts during skeletal muscle regeneration.
        Lab. Invest. 1969; 20: 353-363
        • Ross K.F.A.
        • Jans D.R.
        • Research Committee of the Muscular Dystrophy Group
        The nuclear and cytoplasmic RNA in normally differentiating and dystrophic myoblasts.
        in: Research in Muscular Dystrophy. Proceedings of the 4th Symposium. Pitman, London1968: 240-254
        • Shafiq S.A.
        • Gorycki M.A.
        • Milhorat A.T.
        An electron microscopic study of regeneration and satellite cells in human muscle.
        Neurology (Minneap.). 1967; 17: 567-574
        • Singh I.
        Adenosine triphosphate and muscular contraction and relaxation.
        Nature (Lond.). 1965; 207: 1300
        • Van Breeman V.L.
        Ultrastructure of human muscle, Part 2 (Observations on dystrophic striated muscle fibres).
        Amer. J. Path. 1960; 37: 333-336
        • Walker B.E.
        • Drager G.A.
        Evidence of regeneration in repeat biopsies of dystrophic human muscle.
        Neurology (Minneap.). 1962; 12: 381-384
        • Walton J.N.
        • Adams R.D.
        The response of the normal, the denervated and the dystrophic muscle cell to injury.
        J. Path. Bact. 1956; 72: 273-298
        • Weber A.
        • Herz R.
        The binding of calcium to actomyosin solutions in relation to their biological activity.
        J. biol. Chem. 1963; 238: 599-605
        • Zymaris M.C.
        • Epstein N.
        • Saifer A.
        • Aronson S.M.
        • Volk B.W.
        Distribution of acid-soluble nucleotides in hind leg muscles of mice with “dystrophia muscularis”.
        Amer. J. Physiol. 1959; 196: 1093-1097