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Nonmuscle Myosin II Regulation Directs Its Multiple Roles in Cell Migration and Division.
Garrido-Casado, Marina; Asensio-Juárez, Gloria; Vicente-Manzanares, Miguel.
Afiliación
  • Garrido-Casado M; Molecular Mechanisms Program, Centro de Investigación del Cáncer and Instituto de Biología Molecular y Celular del Cáncer, Consejo Superior de Investigaciones Científicas, University of Salamanca, 37007 Salamanca, Spain; email: miguel.vicente@csic.es.
  • Asensio-Juárez G; Molecular Mechanisms Program, Centro de Investigación del Cáncer and Instituto de Biología Molecular y Celular del Cáncer, Consejo Superior de Investigaciones Científicas, University of Salamanca, 37007 Salamanca, Spain; email: miguel.vicente@csic.es.
  • Vicente-Manzanares M; Molecular Mechanisms Program, Centro de Investigación del Cáncer and Instituto de Biología Molecular y Celular del Cáncer, Consejo Superior de Investigaciones Científicas, University of Salamanca, 37007 Salamanca, Spain; email: miguel.vicente@csic.es.
Annu Rev Cell Dev Biol ; 37: 285-310, 2021 10 06.
Article en En | MEDLINE | ID: mdl-34314591
ABSTRACT
Nonmuscle myosin II (NMII) is a multimeric protein complex that generates most mechanical force in eukaryotic cells. NMII function is controlled at three main levels. The first level includes events that trigger conformational changes that extend the complex to enable its assembly into filaments. The second level controls the ATPase activity of the complex and its binding to microfilaments in extended NMII filaments. The third level includes events that modulate the stability and contractility of the filaments. They all work in concert to finely control force generation inside cells. NMII is a common endpoint of mechanochemical signaling pathways that control cellular responses to physical and chemical extracellular cues. Specific phosphorylations modulate NMII activation in a context-dependent manner. A few kinases control these phosphorylations in a spatially, temporally, and lineage-restricted fashion, enabling functional adaptability to the cellular microenvironment. Here, we review mechanisms that control NMII activity in the context of cell migration and division.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Citoesqueleto / Miosina Tipo II Idioma: En Revista: Annu Rev Cell Dev Biol Asunto de la revista: BIOLOGIA Año: 2021 Tipo del documento: Article

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Citoesqueleto / Miosina Tipo II Idioma: En Revista: Annu Rev Cell Dev Biol Asunto de la revista: BIOLOGIA Año: 2021 Tipo del documento: Article