Literature DB >> 7204497

Density and distribution of alpha-bungarotoxin-binding sites in postsynaptic structures of regenerated rat skeletal muscle.

D Bader.   

Abstract

Acetylcholine receptors (AChR) are organized in a discrete and predictable fashion in the postsynaptic regions of vertebrate skeletal muscle. When muscle is damaged, nerves and myofibers including muscular elements of the endplate degenerate, but the connective tissue elements survive. Muscle fibers regenerate within the basal lamina of the original myofiber. Postsynaptic differentiation in regenerated mammalian skeletal muscle can occur in different ways: (a) at the site of the original endplate in the presence or absence of the nerve, or (b) at ectopic regions of the regenerated myofiber in the presence of the nerve when the original endplate is not present. The present study used (125)I-alpha- bungarotoxin ((125)I-alpha-BuTX) and EM autoradiography to examine the density and distribution of AChR in postsynaptic structures regenerated at the site of the original endplate in the absence of the nerve and at ectopic sites of the myofiber in the presence of the nerve when the original endplate was removed. In regenerated myofibers, the density of alpha-BuTX-binding sites fell within the range of densities observed in uninjured muscle whether postsynaptic differentiation occurred at the site of the original endplate in the absence of the nerve or at an originally ectopic position of the regenerated myofiber. In addition, the distribution of alpha-BuTX-binding sites within the regenerated postsynaptic regions closely resembled the distribution of apha-BuTX- binding sites in uninjured muscle. Morphometric analysis was performed on postsynaptic structures formed at the site of the original endplate in the absence of the nerve or at an ectopic position of the regenerated myofiber by interaction of the nerve and muscle. Although variation in the depth of the primary cleft occurred, there was little difference between the overall structure of regenerated postsynaptic structures and that of endplates of uninjured muscles.

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Year:  1981        PMID: 7204497      PMCID: PMC2111735          DOI: 10.1083/jcb.88.2.338

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  34 in total

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Journal:  Am J Anat       Date:  1973-06

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Authors:  R Miledi; L T Potter
Journal:  Nature       Date:  1971-10-29       Impact factor: 49.962

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Journal:  Physiol Bohemoslov       Date:  1967

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Authors:  D M Fambrough; D B Drachman; S Satyamurti
Journal:  Science       Date:  1973-10-19       Impact factor: 47.728

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Authors:  E A Barnard; J Wieckowski; T H Chiu
Journal:  Nature       Date:  1971-11-26       Impact factor: 49.962

6.  Acetylcholine receptors: number and distribution at neuromuscular junctions in rat diaphragm.

Authors:  D M Fambrough; H C Hartzell
Journal:  Science       Date:  1972-04-14       Impact factor: 47.728

7.  Binding of -bungarotoxin to acetylcholine receptors in mammalian muscle (snake venom-denervated muscle-neonatal muscle-rat diaphragm-SDS-polyacrylamide gel electrophoresis).

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Journal:  Proc Natl Acad Sci U S A       Date:  1972-01       Impact factor: 11.205

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Authors:  B Katz; R Miledi
Journal:  J Physiol       Date:  1972-08       Impact factor: 5.182

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Authors:  H A Padykula; G F Gauthier
Journal:  J Cell Biol       Date:  1970-07       Impact factor: 10.539

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Authors:  R Vracko; E P Benditt
Journal:  J Cell Biol       Date:  1972-11       Impact factor: 10.539

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  12 in total

1.  Molecular forms and localization of acetylcholinesterase and nonspecific cholinesterase in regenerating skeletal muscles.

Authors:  J Sketelj; N Crne; M Brzin
Journal:  Neurochem Res       Date:  1987-02       Impact factor: 3.996

2.  The influence of basal lamina on the accumulation of acetylcholine receptors at synaptic sites in regenerating muscle.

Authors:  U J McMahan; C R Slater
Journal:  J Cell Biol       Date:  1984-04       Impact factor: 10.539

3.  Denervation increases the degradation rate of acetylcholine receptors at end-plates in vivo and in vitro.

Authors:  S Bevan; J H Steinbach
Journal:  J Physiol       Date:  1983-03       Impact factor: 5.182

4.  Treatment with digestive agents reveals several glycoconjugates specifically associated with rat neuromuscular junction.

Authors:  M Iglesias; J Ribera; J E Esquerda
Journal:  Histochemistry       Date:  1992

5.  Extracellular matrix organization in developing muscle: correlation with acetylcholine receptor aggregates.

Authors:  E K Bayne; M J Anderson; D M Fambrough
Journal:  J Cell Biol       Date:  1984-10       Impact factor: 10.539

6.  Cytoskeletal components of the vertebrate neuromuscular junction: vinculin, alpha-actinin, and filamin.

Authors:  R J Bloch; Z W Hall
Journal:  J Cell Biol       Date:  1983-07       Impact factor: 10.539

7.  Degradation rate of acetylcholine receptors inserted into denervated vertebrate neuromuscular junctions.

Authors:  S L Shyng; M M Salpeter
Journal:  J Cell Biol       Date:  1989-02       Impact factor: 10.539

8.  Distribution and turnover rate of acetylcholine receptors throughout the junction folds at a vertebrate neuromuscular junction.

Authors:  M M Salpeter; R Harris
Journal:  J Cell Biol       Date:  1983-06       Impact factor: 10.539

9.  Basal lamina directs acetylcholinesterase accumulation at synaptic sites in regenerating muscle.

Authors:  L Anglister; U J McMahan
Journal:  J Cell Biol       Date:  1985-09       Impact factor: 10.539

10.  Laminin, fibronectin, and collagen in synaptic and extrasynaptic portions of muscle fiber basement membrane.

Authors:  J R Sanes
Journal:  J Cell Biol       Date:  1982-05       Impact factor: 10.539

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