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Semaphorin3A signaling mediated by Fyn-dependent tyrosine phosphorylation of collapsin response mediator protein 2 at tyrosine 32.
Uchida, Yutaka; Ohshima, Toshio; Yamashita, Naoya; Ogawara, Miyuki; Sasaki, Yukio; Nakamura, Fumio; Goshima, Yoshio.
Afiliação
  • Uchida Y; Department of Molecular Pharmacology and Neurobiology, Yokohama City University Graduate School of Medicine, Yokohama 236-0004, Japan.
J Biol Chem ; 284(40): 27393-401, 2009 Oct 02.
Article em En | MEDLINE | ID: mdl-19652227
ABSTRACT
Collapsin response mediator protein 2 (CRMP2) is an intracellular protein that mediates signaling of Semaphorin3A (Sema3A), a repulsive axon guidance molecule. Fyn, a Src-type tyrosine kinase, is involved in the Sema3A signaling. However, the relationship between CRMP2 and Fyn in this signaling pathway is still unknown. In our research, we demonstrated that Fyn phosphorylated CRMP2 at Tyr(32) residues in HEK293T cells. Immunohistochemical analysis using a phospho-specific antibody at Tyr(32) of CRMP showed that Tyr(32)-phosphorylated CRMP was abundant in the nervous system, including dorsal root ganglion neurons, the molecular and Purkinje cell layer of adult cerebellum, and hippocampal fimbria. Overexpression of a nonphosphorylated mutant (Tyr(32) to Phe(32)) of CRMP2 in dorsal root ganglion neurons interfered with Sema3A-induced growth cone collapse response. These results suggest that Fyn-dependent phosphorylation of CRMP2 at Tyr(32) is involved in Sema3A signaling.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Fosfotirosina / Semaforina-3A / Proteínas Proto-Oncogênicas c-fyn / Proteínas do Tecido Nervoso Limite: Animals / Humans Idioma: En Ano de publicação: 2009 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Transdução de Sinais / Fosfotirosina / Semaforina-3A / Proteínas Proto-Oncogênicas c-fyn / Proteínas do Tecido Nervoso Limite: Animals / Humans Idioma: En Ano de publicação: 2009 Tipo de documento: Article