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Ephrin-B1 and ephrin-B2 mediate EphB-dependent presynaptic development via syntenin-1.
McClelland, Andrew C; Sheffler-Collins, Sean I; Kayser, Matthew S; Dalva, Matthew B.
Afiliação
  • McClelland AC; Department of Neuroscience, University of Pennsylvania School of Medicine, 1114 BRBII/III, 421 Curie Boulevard, Philadelphia, PA 19104, USA.
Proc Natl Acad Sci U S A ; 106(48): 20487-92, 2009 Dec 01.
Article em En | MEDLINE | ID: mdl-19915143
ABSTRACT
The development of central nervous system synapses requires precise coordination between presynaptic and postsynaptic components. The EphB family controls postsynaptic development by interacting with glutamate receptors and regulating dendritic filopodia motility, but how EphBs induce the formation of presynaptic specializations is less well understood. Here, we show that knockdown of presynaptic ephrin-B1, ephrin-B2, or syntenin-1, but not ephrin-B3, prevents EphB-dependent presynaptic development. Ephrin-B1, ephrin-B2, and syntenin-1 are clustered together with presynaptic markers, suggesting that these molecules function jointly in presynaptic development. Knockdown of ephrin-B1 or ephrin-B2 reduces the number of synaptic specializations and the colocalization of syntenin-1 with synaptic markers. Simultaneous knockdown of ephrin-B1 and ephrin-B2 suggests that they function independently in the formation of synaptic contacts, but act together to recruit syntenin-1 to presynaptic terminals. Taken together, these results demonstrate that ephrin-B1 and ephrin-B2 function with EphB to mediate presynaptic development via syntenin-1.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistema Nervoso Central / Terminações Pré-Sinápticas / Efrina-B1 / Efrina-B2 / Sinteninas Limite: Animals Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Sistema Nervoso Central / Terminações Pré-Sinápticas / Efrina-B1 / Efrina-B2 / Sinteninas Limite: Animals Idioma: En Revista: Proc Natl Acad Sci U S A Ano de publicação: 2009 Tipo de documento: Article País de afiliação: Estados Unidos