Woronowicz Kamil, Flaumenhaft Robert
The School of Science, Technology, Engineering and Mathematics, Rockland County College, State University of New York (SUNY), Suffern, NY, USA.
Division of Hemostasis and Thrombosis, Department of Medicine, BIDMC, Harvard Medical School, Boston, MA, USA.
Methods Mol Biol. 2025;2887:135-147. doi: 10.1007/978-1-0716-4314-3_9.
The actin cytoskeleton serves an important, but poorly characterized, role in controlling granule exocytosis. The dynamic nature of actin remodeling allows it to act both as a barrier to prevent indiscriminate granule release and as a facilitator of membrane fusion. In its capacity to promote exocytosis, filamentous actin binds to components of the exocytotic machinery through actin binding proteins, but also through direct interactions with SNAREs. The platelet is an excellent cellular model to evaluate SNARE-actin interactions because of the marked reorganization of its actin cytoskeleton that occurs with activation and because of its abundance of secretory granules. This chapter will describe methods to evaluate SNARE-actin interactions in platelets using isolated platelet actin cytoskeleton, granule-enriched membrane fractions in a cell-free secretory system, and purified actin and recombinant SNAREs.
肌动蛋白细胞骨架在控制颗粒胞吐作用中发挥着重要但特征尚不明确的作用。肌动蛋白重塑的动态特性使其既能作为一种屏障防止颗粒随意释放,又能作为膜融合的促进因子。在促进胞吐作用方面,丝状肌动蛋白通过肌动蛋白结合蛋白,也通过与SNARE蛋白的直接相互作用,与胞吐机制的组分结合。由于血小板在激活时其肌动蛋白细胞骨架会发生显著重组,且富含分泌颗粒,因此它是评估SNARE - 肌动蛋白相互作用的极佳细胞模型。本章将描述利用分离的血小板肌动蛋白细胞骨架、无细胞分泌系统中富含颗粒的膜组分以及纯化的肌动蛋白和重组SNARE蛋白来评估血小板中SNARE - 肌动蛋白相互作用的方法。