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J Cell Sci ; 126(Pt 24): 5670-80, 2013 Dec 15.
Artigo em Inglês | MEDLINE | ID: mdl-24127566

RESUMO

Podosomes are actin-based membrane protrusions that facilitate extracellular matrix degradation and motility of invasive cells. Podosomes can self-organize into large rosette-like structures in Src-transformed fibroblasts, osteoclasts and some highly invasive cancer cells. However, the mechanism of this assembly remains obscure. In this study, we show that the suppression of Jun N-terminal kinase (JNK) by the JNK inhibitor SP600125 or short-hairpin RNA inhibited podosome rosette formation in SrcY527F-transformed NIH3T3 fibroblasts. In addition, SrcY527F was less able to induce podosome rosettes in JNK1-null or JNK2-null mouse embryo fibroblasts than in wild-type counterparts. The kinase activity of JNK was essential for promoting podosome rosette formation but not for its localization to podosome rosettes. Moesin, a member of the ERM (ezrin, radixin and moesin) protein family, was identified as a substrate of JNK. We show that the phosphorylation of moesin at Thr558 by JNK was important for podosome rosette formation in SrcY527F-transformed NIH3T3 fibroblasts. Taken together, our results unveil a novel role of JNK in podosome rosette formation through the phosphorylation of moesin.


Assuntos
Fibroblastos/enzimologia , Proteínas dos Microfilamentos/metabolismo , Proteína Quinase 8 Ativada por Mitógeno/metabolismo , Proteína Quinase 9 Ativada por Mitógeno/metabolismo , Processamento de Proteína Pós-Traducional , Quinases da Família src/metabolismo , Animais , Estruturas da Membrana Celular/enzimologia , Citoplasma/enzimologia , Fibroblastos/ultraestrutura , Células HEK293 , Humanos , Camundongos , Células NIH 3T3 , Paxilina/metabolismo , Fosforilação , Transporte Proteico
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