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FMN2 Makes Perinuclear Actin to Protect Nuclei during Confined Migration and Promote Metastasis

机译:FMN2使核仁肌动蛋白在受限的迁移过程中保护细胞核并促进转移

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Cell migration in confined 3D tissue microenvironments is critical for both normal physiological functions and dissemination of tumor cells. We discovered a cytoskeletal structure that prevents damage to the nucleus during migration in confined microenvironments. The formin-family actin filament nucleator FMN2 associates with and generates a perinuclear actin/focal adhesion (FA) system that is distinct from previously characterized actin/FA structures. This system controls nuclear shape and positioning in cells migrating on 2D surfaces. In confined 3D microenvironments, FMN2 promotes cell survival by limiting nuclear envelope damage and DNA double-strand breaks. We found that FMN2 is upregulated in human melanomas and showed that disruption of FMN2 in mouse melanoma cells inhibits their extravasation and metastasis to the lung. Our results indicate a critical role for FMN2 in generating a perinuclear actin/FA system that protects the nucleus and DNA from damage to promote cell survival during confined migration and thus promote cancer metastasis.
机译:在狭窄的3D组织微环境中的细胞迁移对于正常的生理功能和肿瘤细胞的传播都至关重要。我们发现了一种细胞骨架结构,可以防止在受限的微环境中迁移过程中对细胞核的破坏。孔蛋白家族肌动蛋白丝成核剂FMN2与先前的肌动蛋白/ FA结构不同,并与之产生核周肌动蛋白/粘着斑(FA)系统。该系统控制在2D表面上迁移的细胞中的核形状和位置。在受限的3D微环境中,FMN2通过限制核被膜损伤和DNA双链断裂来促进细胞存活。我们发现,FMN2在人黑素瘤中上调,并显示破坏小鼠黑素瘤细胞中的FMN2会抑制其向肺的外渗和转移。我们的结果表明,FMN2在产生核周肌动蛋白/ FA系统中起着至关重要的作用,该系统保护细胞核和DNA不受损害,从而在有限的迁移过程中促进细胞存活,从而促进癌症转移。

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