Structural Motility, Institut Curie, Paris Université Sciences et Lettres, Sorbonne Université, CNRS UMR144, 75005 Paris, France.
Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, MN 55455, USA.
Curr Biol. 2021 May 24;31(10):R586-R602. doi: 10.1016/j.cub.2021.04.005.
Filopodia, microvilli and stereocilia represent an important group of plasma membrane protrusions. These specialized projections are supported by parallel bundles of actin filaments and have critical roles in sensing the external environment, increasing cell surface area, and acting as mechanosensors. While actin-associated proteins are essential for actin-filament elongation and bundling in these protrusions, myosin motors have a surprising role in the formation and extension of filopodia and stereocilia and in the organization of microvilli. Actin regulators and specific myosins collaborate in controlling the length of these structures. Myosins can transport cargoes along the length of these protrusions, and, in the case of stereocilia and microvilli, interactions with adaptors and cargoes can also serve to anchor adhesion receptors to the actin-rich core via functionally conserved motor-adaptor complexes. This review highlights recent progress in understanding the diverse roles myosins play in filopodia, microvilli and stereocilia.
微丝足、微绒毛和静纤毛是细胞膜突起的重要形式。这些特殊的突起由肌动蛋白丝平行束支撑,在感知外部环境、增加细胞表面积和作为机械感受器方面发挥着关键作用。虽然肌动蛋白相关蛋白对于这些突起中的肌动蛋白丝的延伸和聚集是必不可少的,但肌球蛋白在微丝足和静纤毛的形成和延伸以及微绒毛的组织中起着出人意料的作用。肌动蛋白调节剂和特定的肌球蛋白协同控制这些结构的长度。肌球蛋白可以沿着这些突起的长度运输货物,并且在静纤毛和微绒毛的情况下,与衔接蛋白和货物的相互作用也可以通过功能保守的马达-衔接蛋白复合物将粘附受体锚定到富含肌动蛋白的核心。这篇综述强调了最近在理解肌球蛋白在微丝足、微绒毛和静纤毛中的多种作用方面取得的进展。