Literature DB >> 9140698

Common molecular mechanisms in field- and agrin-induced acetylcholine receptor clustering.

F Sabrina1, J Stollberg.   

Abstract

1. The aggregation of acetylcholine receptors at the developing neuromuscular junction is critical to the development and function of this synapse. In vitro studies have shown that receptor aggregation can be induced by the finding of agrin to the muscle cell surface and by the electric field-induced concentration of a (nonreceptor) molecule at the cathodal cell pole. 2. We report here on the interaction between agrin binding and electric fields with respect to the distribution of receptors and agrin binding sites. 3. (a) Pretreatment of cells with agrin completely blocks the development of field-induced receptor clusters. (b) Field-induced aggregation of receptors precedes the field-induced aggregation of agrin binding sites by approximately 30 min. (c) Electric fields prevent agrin-induced receptor clustering despite the presence of agrin binding sites and freely diffusing receptors. 4. These results indicate that another membrane component-but not the agrin binding site and not the receptor-is required for agrin-induced receptor clustering. They also suggest that electric fields and agrin cause receptor clustering via common molecular mechanisms.

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Year:  1997        PMID: 9140698     DOI: 10.1023/a:1026365812496

Source DB:  PubMed          Journal:  Cell Mol Neurobiol        ISSN: 0272-4340            Impact factor:   5.046


  31 in total

1.  Local accumulation of acetylcholine receptors is neither necessary nor sufficient to induce cluster formation.

Authors:  J Stollberg; S E Fraser
Journal:  J Neurosci       Date:  1990-01       Impact factor: 6.167

Review 2.  The role of agrin in synapse formation.

Authors:  M A Bowe; J R Fallon
Journal:  Annu Rev Neurosci       Date:  1995       Impact factor: 12.449

3.  Nerve-induced and spontaneous redistribution of acetylcholine receptors on cultured muscle cells.

Authors:  M J Anderson; M W Cohen
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

4.  Formation of postsynaptic specializations induced by latex beads in cultured muscle cells.

Authors:  H B Peng; P C Cheng
Journal:  J Neurosci       Date:  1982-12       Impact factor: 6.167

5.  Localization of acetylcholine receptor by 125I-labeled alpha-bungarotoxin binding at mouse motor endplates.

Authors:  H C Fertuck; M M Salpeter
Journal:  Proc Natl Acad Sci U S A       Date:  1974-04       Impact factor: 11.205

6.  Distribution of alpha-dystroglycan during embryonic nerve-muscle synaptogenesis.

Authors:  M W Cohen; C Jacobson; E W Godfrey; K P Campbell; S Carbonetto
Journal:  J Cell Biol       Date:  1995-05       Impact factor: 10.539

7.  Membrane-related specializations associated with acetylcholine receptor aggregates induced by electric fields.

Authors:  P W Luther; H B Peng
Journal:  J Cell Biol       Date:  1985-01       Impact factor: 10.539

8.  Motor neurons contain agrin-like molecules.

Authors:  C Magill-Solc; U J McMahan
Journal:  J Cell Biol       Date:  1988-11       Impact factor: 10.539

9.  Identification of agrin, a synaptic organizing protein from Torpedo electric organ.

Authors:  R M Nitkin; M A Smith; C Magill; J R Fallon; Y M Yao; B G Wallace; U J McMahan
Journal:  J Cell Biol       Date:  1987-12       Impact factor: 10.539

10.  Formation of acetylcholine receptor clusters in chick myotubes: migration or new insertion?

Authors:  J M Dubinsky; D J Loftus; G D Fischbach; E L Elson
Journal:  J Cell Biol       Date:  1989-10       Impact factor: 10.539

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  2 in total

1.  Ultrastructure of acetylcholine receptor aggregates parallels mechanisms of aggregation.

Authors:  D D Kunkel; L K Lee; J Stollberg
Journal:  BMC Neurosci       Date:  2001-12-10       Impact factor: 3.288

2.  Mechanistic distinctions between agrin and laminin-1 induced aggregation of acetylcholine receptors.

Authors:  Lara K Lee; Dennis D Kunkel; Jes Stollberg
Journal:  BMC Neurosci       Date:  2002-08-15       Impact factor: 3.288

  2 in total

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