Inhibition of agrin-mediated acetylcholine receptor clustering by utrophin C-terminal peptides
Genes to Cells, ISSN: 1356-9597, Vol: 1, Issue: 8, Page: 755-764
1996
- 9Citations
- 10Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
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Metrics Details
- Citations9
- Citation Indexes9
- CrossRef5
- Captures10
- Readers10
- 10
Article Description
Background: Agrin is an extracellular matrix protein that is required for neuromuscular synaptogenesis and is particularly important in the clustering of acetylcholine receptors at post-synaptic sites. Little is known about the signal transduction pathway of agrin-mediated receptor clustering, although cytoskeletal elements and a dystrophin associated glycoprotein complex (DGC) have been implicated. Because agrin binds to α-dystroglycan, a member of the DGC, and the DGC is linked to actin through utrophin at postsynaptic sites, it has been suggested that binding of utrophin to the DGC plays a central role in agrin mediated receptor clustering. Results: To test this hypothesis, we expressed at high levels the DGC binding domains of utrophin in cultured myotubes using recombinant Semliki Forest Virus. Myotubes expressing the utrophin and dystrophin DGC binding domain formed significantly fewer acetylcholine receptor clusters in response to agrin than myotubes expressing other proteins. Conclusions: These results suggest involvement of the DGC and utrophin in the signal transduction pathway of agrin-mediated acetylcholine receptor cluster formation or stabilization. © Blackwell Science Limited.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0030203095&origin=inward; http://dx.doi.org/10.1111/j.1365-2443.1996.tb00015.x; http://www.ncbi.nlm.nih.gov/pubmed/9077444; https://onlinelibrary.wiley.com/doi/10.1111/j.1365-2443.1996.tb00015.x; https://dx.doi.org/10.1111/j.1365-2443.1996.tb00015.x
Wiley
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