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Actin-propelled Invasive Membrane Protrusions Promote Fusogenic Protein Engagement During Cell-Cell Fusion

机译:肌动蛋白推进入侵细胞膜突起促进促融合蛋白接合过程中细胞 - 细胞融合

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摘要

Cell-cell fusion is critical for the conception, development and physiology of multicellular organisms. Although cellular fusogenic proteins and the actin cytoskeleton are implicated in cell-cell fusion, whether and how they coordinate to promote plasma membrane fusion remain unclear. Here, we reconstituted a high-efficiency, inducible cell-fusion culture system in the normally non-fusing Drosophila S2R+ cells. Both fusogenic proteins and actin cytoskeletal rearrangements were necessary for cell fusion, and, in combination, were sufficient to impart fusion competence. Localized actin polymerization triggered by specific cell-cell or cell-matrix adhesion molecules propelled invasive cell membrane protrusions, which, in turn, promoted fusogenic protein engagement and plasma membrane fusion. This de novo cell-fusion culture system reveals a general role for actin-propelled invasive membrane protrusions in driving fusogenic protein engagement during cell-cell fusion.
机译:细胞-细胞融合对于多细胞生物的概念,发展和生理至关重要。尽管细胞融合蛋白和肌动蛋白细胞骨架与细胞-细胞融合有关,但它们是否以及如何协调以促进质膜融合尚不清楚。在这里,我们在通常不融合的果蝇S2R +细胞中重建了高效的诱导型细胞融合培养系统。融合蛋白和肌动蛋白细胞骨架重排对于细胞融合都是必需的,并且组合起来足以赋予融合能力。由特定的细胞间或细胞基质粘附分子触发的局部肌动蛋白聚合反应推动了浸润性细胞膜突起,继而促进了融合蛋白的结合和质膜融合。这种从头开始的细胞融合培养系统揭示了在细胞与细胞融合过程中,肌动蛋白推动的侵袭性膜突起在驱动融合蛋白参与中的一般作用。

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