This paper is only available as a PDF. To read, Please Download here.
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.
To read this article in full you will need to make a payment
Purchase one-time access:
Academic & Personal: 24 hour online accessCorporate R&D Professionals: 24 hour online accessOne-time access price info
- For academic or personal research use, select 'Academic and Personal'
- For corporate R&D use, select 'Corporate R&D Professionals'
Subscribe:
Subscribe to Journal of the Neurological SciencesAlready a print subscriber? Claim online access
Already an online subscriber? Sign in
Register: Create an account
Institutional Access: Sign in to ScienceDirect
References
Allbrook, D. B. (1968) Personal communication.
- Myogenesis in rat embryos.Bull. Johns Hopk. Hosp. 1962; 110: 187-201
- Le frazioni del fosforo acido-solubile nella distrofia muscolare progressiva.Sperimentale. 1954; 104 (Fasc. xi-xii): 315
- The Satellite Cell of Skeletal Muscle.in: M.D. Thesis. Cambridge University, Cambridge1968
- Satellite cells and skeletal muscle regeneration.Brit. J. Surg. 1966; 53: 638-642
- Regeneration in human skeletal muscle.J. Path. Bact. 1965; 89: 503-512
- Succinic dehydrogenase content of individual muscle fibres at different ages and stages of growth.Life Sci. 1969; 8: 791-808
- In vitro synthesis of native myosin, actin and tropomyosin from embryonic chick polyribosomes.in: Proc. nat. Acad. Sci. (Wash.). 59. 1968: 590-597
- Ultrastructural changes in dystrophic muscle.in: Research in Muscular Dystrophy. Proceedings of the 4th Symposium. Pitman, London1968: 207-222
Hudgson, P. (1969). Personal communication.
- Pre-clinical muscular dystrophy: Histopathological changes observed on muscle biopsy.Brain. 1967; 90: 565-576
- Principles of myopathology as illustrated in the nutritional myopathy of the Rottnest quokka (Setonix brachyurus).Ann. N.Y. Acad. Sci. 1966; 138: 90-101
- Normal and abnormal human muscle in tissue culture.in: Proc. Aust. Ass. Neurol.5. 1968: 79-85
- Morphological relationship of polyribosomes and myosin filaments in developing and regenerating skeletal muscle.Nature (Lond.). 1969; 222: 1168-1169
- The morphological development of chick embryo skeletal muscle grown in tissue culture as studied by electron microscopy.J. neurol. Sci. 1970; 10: 385-405
- Muscle regeneration in normal mice.in: An electron microscope study. 1970 (In preparation)
- Biochemische und elektronenoptische Untersuchungen bei einem Fall von idiopathischer paroxysmaler Myoglobinurie.Beitr. path. Anat. 1966; 134: 65-83
Mastaglia, F. L. (1969) Unpublished observations.
- A histological and histochemical study of skeletal muscle regeneration in polymyositis.J. neurol. Sci. 1970; 10: 471-487
- An electron microscope study of skeletal muscle in polymyositis.1970 (In preparation)
- Regeneration in Duchenne muscular dystrophy: A histological and histochemical study.Brain. 1970; 92: 809-818
- Restricted forms of muscular dystrophy.in: A study of 11 cases. Proc. Aust. Ass. Neurol.6. 1969: 107-121
- Satellite cells of skeletal muscle fibres.J. biophys. biochem. Cytol. 1961; 9: 493-495
- 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
- Das elektronenmikroskopische Bild des Skelettmuskels bei Dystrophia musculorum progressiva Erb.Naturwissenschaften. 1960; 47: 186-187
- 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)
- Regeneration in neuromuscular disorders.in: Proc. of the International Congress on Muscle Diseases, Milan, 1969 Excerpta Medica Foundation, Amsterdam1969 (International Congress Series No. 186)
- Denervated muscle fibres in hereditary mouse dystrophy.J. Neurol. Neurosurg. Psychiat. 1967; 30: 526-530
- Synthesis of skeletal muscle proteins in early embryos and regenerating tissue of chick and Triturus.Exp. Cell Res. 1962; 26: 269-277
- Tissue culture and electron microscopy in muscle disease.in: Walton J.N. Disorders of Voluntary Muscle. Churchill, London1964
- Electron microscopy in the study of muscular dystrophy.Ann. N.Y. Acad. Sci. 1966; 138: 138-150
- Histopathological features of muscle in the preclinical stages of muscular dystrophy.Brain. 1962; 85: 109-120
- Ultrastructural alterations in skeletal muscle fibres injured by cold.Lab. Invest. 1964; 13: 1279-1302
- Origin of myoblasts during skeletal muscle regeneration.Lab. Invest. 1969; 20: 353-363
- 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
- An electron microscopic study of regeneration and satellite cells in human muscle.Neurology (Minneap.). 1967; 17: 567-574
- Adenosine triphosphate and muscular contraction and relaxation.Nature (Lond.). 1965; 207: 1300
- Ultrastructure of human muscle, Part 2 (Observations on dystrophic striated muscle fibres).Amer. J. Path. 1960; 37: 333-336
- Evidence of regeneration in repeat biopsies of dystrophic human muscle.Neurology (Minneap.). 1962; 12: 381-384
- The response of the normal, the denervated and the dystrophic muscle cell to injury.J. Path. Bact. 1956; 72: 273-298
- The binding of calcium to actomyosin solutions in relation to their biological activity.J. biol. Chem. 1963; 238: 599-605
- Distribution of acid-soluble nucleotides in hind leg muscles of mice with “dystrophia muscularis”.Amer. J. Physiol. 1959; 196: 1093-1097
Article info
Publication history
Received:
November 21,
1969
Identification
Copyright
© 1970 Published by Elsevier Inc.