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| Research article summary (published 29 May 2009): |
Regulation of acetylcholine receptor clustering by ADF/cofilin-directed vesicular trafficking.
Full Abstract
Postsynaptic receptor localization is crucial for synapse development and function, but the underlying cytoskeletal mechanisms remain elusive. Using Xenopus neuromuscular junctions as a model, we found that actin depolymerizing factor (ADF)/cofilin regulated actin-dependent vesicular trafficking of acetylcholine receptors (AChRs) to the postsynaptic membrane. Active ADF/cofilin was concentrated in small puncta adjacent to AChR clusters and was spatiotemporally correlated with the formation and maintenance of surface AChR clusters. Notably, increased actin dynamics, vesicular markers and intracellular AChRs were all enriched at the sites of ADF/cofilin localization. Furthermore, a substantial amount of new AChRs was detected at these ADF/cofilin-enriched sites. Manipulation of either ADF/cofilin activity through its serine-3 phosphorylation or ADF/cofilin localization via 14-3-3 proteins markedly attenuated AChR insertion and clustering. These results suggest that spatiotemporally restricted ADF/cofilin-mediated actin dynamics regulate AChR trafficking during the development of neuromuscular synapses.
Author information
Author/s: Lee, Chi Wai (CW); Han, Jianzhong (J); Bamburg, James R (JR); Han, Liang (L); Lynn, Rachel (R); Zheng, James Q (JQ);
Affiliation: Department of Cell Biology, Emory University School of Medicine, Atlanta, Georgia, USA.
Grants: AG029596 (Agency:NIA NIH HHS) ; GM083889 (Agency:NIGMS NIH HHS) ; NS40371 (Agency:NINDS NIH HHS)
Journal and publication information
Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
Journal: Nature neuroscience (Nat Neurosci), published in United States. (Language: eng)
Reference: 2009-Jul; vol 12 (issue 7) : pp 848-56
Dates: Created 2009/06/25; Completed 2009/07/07; Revised 2009/07/23;
PMID: 19483689, status: MEDLINE (last retrieval date: 8/20/2009, IMS Date: )
Sourced from the National Library of Medicine. Abstract text and other information may be subject to copyright.
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