Your browser doesn't support javascript.
loading
A simple active fluid model unites cytokinesis, cell crawling, and axonal outgrowth.
Craig, Erin M; Oprea, Francesca; Alam, Sajid; Grodsky, Ania; Miller, Kyle E.
Afiliação
  • Craig EM; Central Washington University, Department of Physics, 400 E. University Way, Ellensburg, WA 98926-7422, USA.
  • Oprea F; Department of Integrative Biology, Michigan State University, East Lansing, MI 48824, USA.
  • Alam S; Department of Integrative Biology, Michigan State University, East Lansing, MI 48824, USA.
  • Grodsky A; Department of Integrative Biology, Michigan State University, East Lansing, MI 48824, USA.
  • Miller KE; Department of Integrative Biology, Michigan State University, East Lansing, MI 48824, USA.
bioRxiv ; 2024 May 23.
Article em En | MEDLINE | ID: mdl-38826455
ABSTRACT
Axonal outgrowth, cell crawling, and cytokinesis utilize actomyosin, microtubule-based motors, cytoskeletal dynamics, and substrate adhesions to produce traction forces and bulk cellular motion. While it has long been appreciated that growth cones resemble crawling cells and that the mechanisms that drive cytokinesis help power cell crawling, they are typically viewed as unique processes. To better understand the relationship between these modes of motility, here, we developed a unified active fluid model of cytokinesis, amoeboid migration, mesenchymal migration, neuronal migration, and axonal outgrowth in terms of cytoskeletal flow, adhesions, viscosity, and force generation. Using numerical modeling, we fit subcellular velocity profiles of the motions of cytoskeletal structures and docked organelles from previously published studies to infer underlying patterns of force generation and adhesion. Our results indicate that, during cytokinesis, there is a primary converge zone at the cleavage furrow that drives flow towards it; adhesions are symmetric across the cell, and as a result, cells are stationary. In mesenchymal, amoeboid, and neuronal migration, the site of the converge zone shifts, and differences in adhesion between the front and back of the cell drive crawling. During neuronal migration and axonal outgrowth, the primary convergence zone lies within the growth cone, which drives actin retrograde flow in the P-domain and bulk anterograde flow of the axonal shaft. They differ in that during neuronal migration, the cell body is weakly attached to the substrate and thus moves forward at the same velocity as the axon. In contrast, during axonal outgrowth, the cell body strongly adheres to the substrate and remains stationary, resulting in a decrease in flow velocity away from the growth cone. The simplicity with which cytokinesis, cell crawling, and axonal outgrowth can be modeled by varying coefficients in a simple model suggests a deep connection between them.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article