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SynGAP Regulates Steady-State and Activity-Dependent Phosphorylation of Cofilin

Carlisle, Holly J. and Manzerra, Pasquale and Marcora, Edoardo and Kennedy, Mary B. (2008) SynGAP Regulates Steady-State and Activity-Dependent Phosphorylation of Cofilin. Journal of Neuroscience, 28 (50). pp. 13673-13683. ISSN 0270-6474. PMCID PMC2615239. https://resolver.caltech.edu/CaltechAUTHORS:CARjns08

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Abstract

SynGAP, a prominent Ras/Rap GTPase-activating protein in the postsynaptic density, regulates the timing of spine formation and trafficking of glutamate receptors in cultured neurons. However, the molecular mechanisms by which it does this are unknown. Here, we show that synGAP is a key regulator of spine morphology in adult mice. Heterozygous deletion of synGAP was sufficient to cause an excess of mushroom spines in adult brains, indicating that synGAP is involved in steady-state regulation of actin in mature spines. Both Ras- and Rac-GTP levels were elevated in forebrains from adult synGAP+/- mice. Rac is a well known regulator of actin polymerization and spine morphology. The steady-state level of phosphorylation of cofilin was also elevated in synGAP+/- mice. Cofilin, an F-actin severing protein that is inactivated by phosphorylation, is a downstream target of a pathway regulated by Rac. We show that transient regulation of cofilin by treatment with NMDA is also disrupted in synGAP mutant neurons. Treatment of wild-type neurons with 25 µM NMDA triggered transient dephosphorylation and activation of cofilin within 15 s. In contrast, neurons cultured from mice with a homozygous or heterozygous deletion of synGAP lacked the transient regulation by the NMDA receptor. Depression of EPSPs induced by a similar treatment of hippocampal slices with NMDA was disrupted in slices from synGAP+/- mice. Our data show that synGAP mediates a rate-limiting step in steady-state regulation of spine morphology and in transient NMDA-receptor-dependent regulation of the spine cytoskeleton.


Item Type:Article
Related URLs:
URLURL TypeDescription
http://dx.doi.org/10.1523/JNEUROSCI.4695-08.200DOIArticle
http://www.jneurosci.org/cgi/content/abstract/28/50/13673PublisherArticle
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2615239/PubMed CentralArticle
ORCID:
AuthorORCID
Kennedy, Mary B.0000-0003-1369-0525
Additional Information:Copyright © 2008 Society for Neuroscience. Received Sept. 30, 2008; accepted Oct. 27, 2008. This work was supported by National Institutes of Health (NIH) Grant NS17660 to M.B.K., by NIH Dorothy Kirschstein Fellowship F32NS47894 to H.J.C., and by donations to Caltech from Parna L. Joyce, Nancy A.E. Hicks, and the Gordon and Betty Moore Foundation. We thank Dr. Joshua Sanes (Harvard, Cambridge, MA) for GFP line-M transgenic mice, Dr. Brent Lindquist (Stony Brook University, Stony Brook, NY) for 3DMA spine analysis software, and Alan Rosenstein and Leslie Schenker for technical assistance.
Funders:
Funding AgencyGrant Number
NIHNS17660
NIHF32NS47894
Parna L. JoyceUNSPECIFIED
Nancy A.E. HicksUNSPECIFIED
Gordon and Betty Moore FoundationUNSPECIFIED
Subject Keywords:cytoskeleton; actin; spines; LTD; Ras; Rac
Issue or Number:50
PubMed Central ID:PMC2615239
Record Number:CaltechAUTHORS:CARjns08
Persistent URL:https://resolver.caltech.edu/CaltechAUTHORS:CARjns08
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:12706
Collection:CaltechAUTHORS
Deposited By: Archive Administrator
Deposited On:21 Dec 2008 00:47
Last Modified:03 Oct 2019 00:31

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