Document Detail


Acetylcholine receptor clustering and triton solubility: neural effect.
MedLine Citation:
PMID:  3351508     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Previous studies by Prives et al. (1980, 1982a and b) have shown that acetylcholine receptors (AchRs) are extracted from muscle cells in vitro by Triton X-100 at different rates, and that clustered receptors extract most slowly. The present study was aimed at comparing the relative extractability of receptors in clusters with those in intercluster regions and the role of neural factors in regulating this extractability. Using primary rat muscle cells in vitro we confirmed that receptor extraction with Triton X-100 does not fit a single exponential but has more than one rate, and that in control cells clustered receptors extract more slowly than do receptors in intercluster regions. The major new observation in this study was that neural extract lowered the overall Triton extraction rate of intercluster receptors to that of clustered receptors. Additional new observations include the findings that (1) both clustered and intercluster receptors show multiphasic extraction rates; (2) stabilization of AchRs against Triton extraction increases with time in the surface membrane; (3) the effect of neural extract on Triton extractability of AChR is dependent on factors that control RNA synthesis, cytoskeletal elements, and collagen; (4) fixation and/or buffer washes accelerate receptor extraction only in cells that are treated with Triton, but not in control cells; (5) in control cells (not exposed to neural factors) Triton X-100 causes new clusters to form. From experiments using Con A we suggest that the Triton-induced new clusters may not be formed by a redistribution of receptors but are, most likely, due to the presence of groups of intercluster receptors with extraction rates lower than those of surrounding receptors.
Authors:
T R Podleski; M M Salpeter
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Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Journal of neurobiology     Volume:  19     ISSN:  0022-3034     ISO Abbreviation:  J. Neurobiol.     Publication Date:  1988 Mar 
Date Detail:
Created Date:  1988-05-10     Completed Date:  1988-05-10     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  0213640     Medline TA:  J Neurobiol     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  167-85     Citation Subset:  IM    
Affiliation:
Section of Neurobiology and Behavior, Cornell University, Ithaca, New York 14853.
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MeSH Terms
Descriptor/Qualifier:
Aminopropionitrile / pharmacology
Animals
Animals, Newborn / physiology
Autoradiography
Brain
Cytochalasins / pharmacology
Dactinomycin / pharmacology
Detergents / pharmacology*
Fetus / physiology
Muscles / analysis
Octoxynol
Polyethylene Glycols / pharmacology*
Rats
Receptors, Cholinergic / analysis*,  drug effects
Solubility
Surface-Active Agents / pharmacology*
Time Factors
Grant Support
ID/Acronym/Agency:
GM 10422/GM/NIGMS NIH HHS; NS 14679/NS/NINDS NIH HHS
Chemical
Reg. No./Substance:
0/Cytochalasins; 0/Detergents; 0/Polyethylene Glycols; 0/Receptors, Cholinergic; 0/Surface-Active Agents; 151-18-8/Aminopropionitrile; 50-76-0/Dactinomycin; 9002-93-1/Octoxynol

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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