Literature DB >> 874836

The distribution of alpha-bungarotoxin binding sites of mammalian skeletal muscle developing in vivo.

S Bevan, J H Steinbach.   

Abstract

1. The distribution of alpha-bungarotoxin binding sites on embryonic and neonatal rat skeletal muscle fibres was determined by autoradiography. Most of the bungarotoxin binding could be inhibited by curare. This observation, together with the spatial distribution of toxin-binding sites, indicates that the distribution of bound toxin reflects that of acetylcholine (ACh) receptors on these developing muscle cells.2. At 15 days of embryogenesis, muscle fibres showed an essentially uniform distribution of receptors. By 16 days, many fibres showed an accumulation of receptors in their mid-region. This accumulation was at the same location as histochemically demonstrated cholinesterase activity.3. At 16 days ACh receptors were distributed over the entire length of the fibres, with a gradient of increasing density as the accumulation was appoached. The density of toxin binding sites in the accumulation was greater than the general level on 15 day cells, suggesting that the high junctional density does not develop solely by the loss of extrajunctional receptors.4. The accumulations of ACh receptors became more pronounced and circumscribed with embryonic development, and after birth the extent of the localizations appeared to follow the size of the neuromuscular junction. The extrajunctional receptor density decreased with development, and by 1 week after birth was undetectable by the methods used.5. The results suggest that the high junctional receptor density found on adult, innervated skeletal muscle fibres develops after the formation of the neuromuscular junction.

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Year:  1977        PMID: 874836      PMCID: PMC1283609          DOI: 10.1113/jphysiol.1977.sp011808

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  34 in total

1.  A "DIRECT-COLORING" THIOCHOLINE METHOD FOR CHOLINESTERASES.

Authors:  M J KARNOVSKY; L ROOTS
Journal:  J Histochem Cytochem       Date:  1964-03       Impact factor: 2.479

2.  Steps in the neoplastic transformation of hamster embryo cells by polyoma virus.

Authors:  M VOGT; R DULBECCO
Journal:  Proc Natl Acad Sci U S A       Date:  1963-02-15       Impact factor: 11.205

3.  Junctional and extra-junctional acetylcholine receptors in skeletal muscle fibres.

Authors:  R MILEDI
Journal:  J Physiol       Date:  1960-04       Impact factor: 5.182

4.  [Normal and pathological structural variations of the myoneural junction].

Authors:  C COERS
Journal:  Acta Neurol Psychiatr Belg       Date:  1955-10

5.  [Displacement of specific cholinesterase during the development of muscular innervation].

Authors:  J ZELENA; J SZENTAGOTHAI
Journal:  Acta Histochem       Date:  1957-03-30       Impact factor: 2.479

Review 6.  Inductive functions of the nervous system.

Authors:  A J Harris
Journal:  Annu Rev Physiol       Date:  1974       Impact factor: 19.318

7.  Correlation of grain counts with radioactivity (125I and tritium) in autoradiography.

Authors:  G L Ada; J H Humphrey; B A Askonas; H O McDevitt; G J Nossal
Journal:  Exp Cell Res       Date:  1966-03       Impact factor: 3.905

8.  Neuromuscular transmission in new-born rats.

Authors:  P A Redfern
Journal:  J Physiol       Date:  1970-08       Impact factor: 5.182

9.  The binding of tetrodotoxin and alpha-bungarotoxin to normal and denervated mammalian muscle.

Authors:  D Colquhoun; H P Rang; J M Ritchie
Journal:  J Physiol       Date:  1974-07       Impact factor: 5.182

10.  Control of ACh sensitivity by muscle activity in the rat.

Authors:  T Lomo; J Rosenthal
Journal:  J Physiol       Date:  1972-03       Impact factor: 5.182

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  66 in total

1.  Developmental changes in the half-life of acetylcholine receptors in the myotomal muscle of Xenopus laevis.

Authors:  M W Cohen; P F Frair; C Cantin; G Hébert
Journal:  J Physiol       Date:  1990-07       Impact factor: 5.182

2.  Differences in expression of acetylcholinesterase and collagen Q control the distribution and oligomerization of the collagen-tailed forms in fast and slow muscles.

Authors:  E Krejci; C Legay; S Thomine; J Sketelj; J Massoulié
Journal:  J Neurosci       Date:  1999-12-15       Impact factor: 6.167

3.  Apparent acetylcholine receptor channel conversion at individual rat soleus end-plates in vitro.

Authors:  S M Schuetze; S Vicini
Journal:  J Physiol       Date:  1986-06       Impact factor: 5.182

Review 4.  Myasthenia gravis: an autoimmune response against the acetylcholine receptor.

Authors:  Y M Graus; M H De Baets
Journal:  Immunol Res       Date:  1993       Impact factor: 2.829

Review 5.  To build a synapse: signaling pathways in neuromuscular junction assembly.

Authors:  Haitao Wu; Wen C Xiong; Lin Mei
Journal:  Development       Date:  2010-04       Impact factor: 6.868

6.  Early GABA(A) receptor clustering during the development of the rostral nucleus of the solitary tract.

Authors:  W L Heck; A M Basaraba; A Slusarczyk; L Schweitzer
Journal:  J Anat       Date:  2003-04       Impact factor: 2.610

7.  Aberrant patterning of neuromuscular synapses in choline acetyltransferase-deficient mice.

Authors:  Eugene P Brandon; Weichun Lin; Kevin A D'Amour; Donald P Pizzo; Bertha Dominguez; Yoshie Sugiura; Silke Thode; Chien-Ping Ko; Leon J Thal; Fred H Gage; Kuo-Fen Lee
Journal:  J Neurosci       Date:  2003-01-15       Impact factor: 6.167

8.  Altered developmental changes of neuromuscular junction in hypo- and hyperthyroid rats.

Authors:  K Kawa; K Obata
Journal:  J Physiol       Date:  1982-08       Impact factor: 5.182

9.  Neural regulation of acetylcholine receptors in rat neonatal muscle.

Authors:  L L Bambrick; T Gordon
Journal:  J Physiol       Date:  1992-04       Impact factor: 5.182

10.  Degradation of junctional and extrajunctional acetylcholine receptors by developing rat skeletal muscle.

Authors:  J H Steinbach; J Merlie; S Heinemann; R Bloch
Journal:  Proc Natl Acad Sci U S A       Date:  1979-07       Impact factor: 11.205

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