Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Mais filtros

Base de dados
Ano de publicação
Tipo de documento
Intervalo de ano de publicação
1.
J Cell Physiol ; 222(3): 612-24, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-19927303

RESUMO

Development is punctuated by morphogenetic rearrangements of epithelial tissues, including detachment of motile cells during epithelial-mesenchymal transition (EMT). Dramatic actin rearrangements occur as cell-cell junctions are dismantled and cells become independently motile during EMT. Characterizing dynamic actin rearrangements and identifying actin machinery driving these rearrangements is essential for understanding basic mechanisms of cell-cell junction remodeling. Using immunofluorescence and live cell imaging of scattering MDCK cells we examine dynamic actin rearrangement events during EMT and demonstrate that zyxin-VASP complexes mediate linkage of dynamic medial actin networks to adherens junction (AJ) membranes. A functional analysis of zyxin in EMT reveals its role in regulating disruption of actin membrane linkages at cell-cell junctions, altering cells' ability to fully detach and migrate independently during EMT. Expression of a constitutively active zyxin mutant results in persistent actin-membrane linkages and cell migration without loss of cell-cell adhesion. We propose zyxin functions in morphogenetic rearrangements, maintaining collective migration by transducing individual cells' movements through AJs, thus preventing the dissociation of individual migratory cells.


Assuntos
Actinas/metabolismo , Junções Aderentes/metabolismo , Movimento Celular , Transdiferenciação Celular , Proteínas do Citoesqueleto/metabolismo , Células Epiteliais/metabolismo , Mesoderma/metabolismo , Animais , Adesão Celular , Moléculas de Adesão Celular/metabolismo , Linhagem Celular , Forma Celular , Proteínas do Citoesqueleto/genética , Cães , Imunofluorescência , Fator de Crescimento de Hepatócito/metabolismo , Mesoderma/citologia , Proteínas dos Microfilamentos/metabolismo , Microscopia de Fluorescência , Microscopia de Vídeo , Mutação , Fosfoproteínas/metabolismo , Interferência de RNA , Fatores de Tempo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA