MRC - Laboratory for Molecular Cell Biology, University College London, London WC1E 6BT, UK.
Institute for Bioengineering of Catalonia (IBEC), The Barcelona Institute for Science and Technology (BIST), Barcelona 08028, Spain.
Dev Cell. 2018 Apr 9;45(1):132-145.e3. doi: 10.1016/j.devcel.2018.03.009.
Animal cells undergo a dramatic series of shape changes as they divide, which depend on re-modeling of cell-substrate adhesions. Here, we show that while focal adhesion complexes are disassembled during mitotic rounding, integrins remain in place. These integrin-rich contacts connect mitotic cells to the underlying substrate throughout mitosis, guide polarized cell migration following mitotic exit, and are functionally important, since adherent cells undergo division failure when removed from the substrate. Further, the ability of cells to re-spread along pre-existing adhesive contacts is essential for division in cells compromised in their ability to construct a RhoGEF-dependent (Ect2) actomyosin ring. As a result, following Ect2 depletion, cells fail to divide on small adhesive islands but successfully divide on larger patterns, as the connection between daughter cells narrows and severs as they migrate away from one another. In this way, regulated re-modeling of cell-substrate adhesions during mitotic rounding aids division in animal cells.
动物细胞在分裂过程中会经历一系列剧烈的形态变化,这取决于细胞-基质黏附的重塑。在这里,我们表明,虽然在有丝分裂过程中焦点黏附复合物被解体,但整合素仍然存在。这些富含整合素的接触将有丝分裂细胞与下面的基质连接起来,在有丝分裂后引导极化细胞迁移,并具有功能重要性,因为当细胞从基质上移除时,黏附的细胞会发生分裂失败。此外,细胞能够沿着预先存在的黏附接触重新扩散,对于那些构建 RhoGEF 依赖性(Ect2)肌动球蛋白环能力受损的细胞的分裂是必不可少的。因此,在 Ect2 耗尽后,细胞在小的黏附岛上将无法分裂,但在更大的图案上可以成功分裂,因为当子细胞彼此远离时,它们之间的连接变窄并切断。通过这种方式,有丝分裂过程中细胞-基质黏附的调节重塑有助于动物细胞的分裂。