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离心力驱动核迁移揭示了 LINC 复合物维持核定位的多种机制。

Centrifugal Displacement of Nuclei Reveals Multiple LINC Complex Mechanisms for Homeostatic Nuclear Positioning.

机构信息

Department of Pathology and Cell Biology, Columbia University, 630 West 168(th) Street, New York, NY 10032, USA.

Department of Pathology and Cell Biology, Columbia University, 630 West 168(th) Street, New York, NY 10032, USA.

出版信息

Curr Biol. 2017 Oct 23;27(20):3097-3110.e5. doi: 10.1016/j.cub.2017.08.073. Epub 2017 Oct 5.

Abstract

Nuclear movement is critical for developmental events, cell polarity, and migration and is usually mediated by linker of nucleoskeleton and cytoskeleton (LINC) complexes connecting the nucleus to cytoskeletal elements. Compared to active nuclear movement, relatively little is known about homeostatic positioning of nuclei, including whether it is an active process. To explore homeostatic nuclear positioning, we developed a method to displace nuclei in adherent cells using centrifugal force. Nuclei displaced by centrifugation rapidly recentered by mechanisms that depended on cell context. In cell monolayers with wounds oriented orthogonal to the force, nuclei were displaced toward the front and back of the cells on the two sides of the wound. Nuclei recentered from both positions, but at different rates and with different cytoskeletal linkage mechanisms. Rearward recentering was actomyosin, nesprin-2G, and SUN2 dependent, whereas forward recentering was microtubule, dynein, nesprin-2G, and SUN1 dependent. Nesprin-2G engaged actin through its N terminus and microtubules through a novel dynein interacting site near its C terminus. Both activities were necessary to maintain nuclear position in uncentrifuged cells. Thus, even when not moving, nuclei are actively maintained in position by engaging the cytoskeleton through the LINC complex.

摘要

核运动对于发育事件、细胞极性和迁移至关重要,通常由连接核与细胞骨架成分的核骨架-细胞骨架连接(LINC)复合物介导。与活跃的核运动相比,人们对核的平衡定位(包括它是否是一个主动过程)知之甚少。为了探索核的平衡定位,我们开发了一种使用离心力使贴壁细胞中的核移位的方法。通过依赖细胞环境的机制,离心移位的核迅速重新定位。在与力正交的伤口的细胞单层中,细胞核被移向伤口两侧细胞的前后。核从两个位置重新定位,但速度不同,细胞骨架连接机制也不同。向后重新定位依赖于肌动蛋白、nesprin-2G 和 SUN2,而向前重新定位依赖于微管、动力蛋白、nesprin-2G 和 SUN1。nesprin-2G 通过其 N 端与肌动蛋白结合,通过其 C 端附近的一个新的动力蛋白相互作用位点与微管结合。这两种活性对于维持未离心细胞中的核位置都是必需的。因此,即使不移动,核也通过 LINC 复合物与细胞骨架相互作用而被主动维持在其位置。

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