Your browser doesn't support javascript.
loading
Reduced PaxillinB localization to cell-substrate adhesions promotes cell migration in Dictyostelium.
Fierro Morales, Julio C; Redfearn, Chandler; Titus, Margaret A; Roh-Johnson, Minna.
Afiliación
  • Fierro Morales JC; Department of Biochemistry, University of Utah, Salt Lake City, UT, 84112, USA.
  • Redfearn C; Department of Kinesiology, North Carolina Agricultural and Technical State University, Greensboro, NC 27411, USA.
  • Titus MA; Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455, USA.
  • Roh-Johnson M; Department of Biochemistry, University of Utah, Salt Lake City, UT, 84112, USA.
bioRxiv ; 2024 Mar 22.
Article en En | MEDLINE | ID: mdl-38562712
ABSTRACT
Many cells adhere to extracellular matrix for efficient cell migration. This adhesion is mediated by focal adhesions, a protein complex linking the extracellular matrix to the intracellular cytoskeleton. Focal adhesions have been studied extensively in mesenchymal cells, but recent research in physiological contexts and amoeboid cells suggest focal adhesion regulation differs from the mesenchymal focal adhesion paradigm. We used Dictyostelium discoideum to uncover new mechanisms of focal adhesion regulation, as Dictyostelium are amoeboid cells that form focal adhesion-like structures for migration. We show that PaxillinB, the Dictyostelium homologue of Paxillin, localizes to dynamic focal adhesion-like structures during Dictyostelium migration. Unexpectedly, reduced PaxillinB recruitment to these structures increases Dictyostelium cell migration. Quantitative analysis of focal adhesion size and dynamics show that lack of PaxillinB recruitment to focal adhesions does not alter focal adhesion size, but rather increases focal adhesion turnover. These findings are in direct contrast to Paxillin function at focal adhesions during mesenchymal migration, challenging the established focal adhesion model.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos