A δ-Catenin Signaling Pathway Leading to Dendritic Protrusions

被引:58
作者
Abu-Elneel, Kawther [2 ,3 ]
Ochiishi, Tomoyo [1 ]
Medina, Miguel [2 ,3 ]
Remedi, Monica [4 ]
Gastaldi, Laura [4 ]
Caceres, Alfredo [4 ]
Kosik, Kenneth S. [2 ,3 ]
机构
[1] Natl Inst Adv Ind Sci & Technol, Mol Neurobiol Grp, Neurosci Res Inst, Tsukuba, Ibaraki 3058566, Japan
[2] Univ Calif Santa Barbara, Neurosci Res Inst, Santa Barbara, CA 93106 USA
[3] Univ Calif Santa Barbara, Dept Mol Cellular & Dev Biol, Santa Barbara, CA 93106 USA
[4] Consejo Nacl Invest Cient & Tecn, Inst Invest Med Mercedes & Martin Ferreya, RA-5000 Cordoba, Argentina
关键词
D O I
10.1074/jbc.M804688200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
delta-Catenin is a synaptic adherens junction protein pivotally positioned to serve as a signaling sensor and integrator. Expression of delta-catenin induces filopodia-like protrusions in neurons. Here we show that the small GTPases of the Rho family act coordinately as downstream effectors of delta-catenin. A dominant negative Rac prevented delta-catenin-induced protrusions, and Cdc42 activity was dramatically increased by delta-catenin expression. A kinase dead LIMK (LIM kinase) and a mutant Cofilin also prevented delta-catenin-induced protrusions. To link the effects of delta-catenin to a physiological pathway, we noted that (S)-3,5-dihydroxyphenylglycine (DHPG) activation of metabotropic glutamate receptors induced dendritic protrusions that are very similar to those induced by delta-catenin. Furthermore, delta-catenin RNA-mediated interference can block the induction of dendritic protrusions by DHPG. Interestingly, DHPG dissociated PSD-95 and N-cadherin from the delta-catenin complex, increased the association of delta-catenin with Cortactin, and induced the phosphorylation of delta-catenin within the sites that bind to these protein partners.
引用
收藏
页码:32781 / 32791
页数:11
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