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本文引用的文献

1
Reticular adhesions are a distinct class of cell-matrix adhesions that mediate attachment during mitosis.网状黏附是一类独特的细胞-基质黏附,在有丝分裂过程中介导黏附。
Nat Cell Biol. 2018 Nov;20(11):1290-1302. doi: 10.1038/s41556-018-0220-2. Epub 2018 Oct 22.
2
Cell adhesion is regulated by CDK1 during the cell cycle.细胞黏附受细胞周期中 CDK1 的调控。
J Cell Biol. 2018 Sep 3;217(9):3203-3218. doi: 10.1083/jcb.201802088. Epub 2018 Jun 21.
3
Regulation of cell cycle progression by cell-cell and cell-matrix forces.细胞-细胞和细胞-基质力对细胞周期进程的调控。
Nat Cell Biol. 2018 Jun;20(6):646-654. doi: 10.1038/s41556-018-0107-2. Epub 2018 May 25.
4
Mitosis-Resistant Adhesions Provide Molecular Memory to Dividing Cells.抗有丝分裂黏附提供了分裂细胞的分子记忆。
Dev Cell. 2018 Apr 9;45(1):5-7. doi: 10.1016/j.devcel.2018.03.015.
5
The Role of Mitotic Cell-Substrate Adhesion Re-modeling in Animal Cell Division.有丝分裂细胞-细胞外基质黏附重塑在动物细胞分裂中的作用。
Dev Cell. 2018 Apr 9;45(1):132-145.e3. doi: 10.1016/j.devcel.2018.03.009.
6
Variation in traction forces during cell cycle progression.细胞周期进程中牵引力的变化。
Biol Cell. 2018 Apr;110(4):91-96. doi: 10.1111/boc.201800006. Epub 2018 Mar 12.
7
Spatio-temporally separated cortical flows and spindle geometry establish physical asymmetry in fly neural stem cells.时空分离的皮质流和纺锤体几何形状在果蝇神经干细胞中建立了物理不对称性。
Nat Commun. 2017 Nov 9;8(1):1383. doi: 10.1038/s41467-017-01391-w.
8
FAK inhibitors induce cell multinucleation and dramatically increase pro-tumoral cytokine expression in RAW 264.7 macrophages.黏着斑激酶(FAK)抑制剂可诱导细胞多核化,并显著增加RAW 264.7巨噬细胞中促肿瘤细胞因子的表达。
FEBS Lett. 2017 Dec;591(23):3861-3871. doi: 10.1002/1873-3468.12895. Epub 2017 Nov 24.
9
Cell Polarity Regulates Biased Myosin Activity and Dynamics during Asymmetric Cell Division via Drosophila Rho Kinase and Protein Kinase N.细胞极性通过果蝇 Rho 激酶和蛋白激酶 N 调控不对称细胞分裂中的偏向肌球蛋白活性和动力学。
Dev Cell. 2017 Jul 24;42(2):143-155.e5. doi: 10.1016/j.devcel.2017.06.012. Epub 2017 Jul 14.
10
Cytokinesis in Metazoa and Fungi.动物界和真菌中的胞质分裂。
Cold Spring Harb Perspect Biol. 2017 Oct 3;9(10):a022343. doi: 10.1101/cshperspect.a022343.

细胞分裂过程中黏附与收缩的平衡。

The balance between adhesion and contraction during cell division.

机构信息

Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN 37232, USA.

Department of Cell and Developmental Biology, SUNY Upstate Medical University, Syracuse, NY 13210, USA; Department of Biology, Syracuse University, Syracuse, NY 13210, USA.

出版信息

Curr Opin Cell Biol. 2019 Feb;56:45-52. doi: 10.1016/j.ceb.2018.09.001. Epub 2018 Sep 28.

DOI:10.1016/j.ceb.2018.09.001
PMID:30268802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6363874/
Abstract

The ability to divide is a fundamental property of a living cell. The 3D orientation of cell division is essential for embryogenesis, maintenance of tissue organization and architecture, as well as controlling cell fate. Much attention has been placed on the mitotic spindle's role in placing itself along the cell's longest axis, where a shape sensing mechanism between a population of microtubules extending from mitotic centrosomes to the cell cortex occurs. However, contractile forces at the cell cortex also likely play a decisive role in determining the final placement of daughter cells following division. In this review, we discuss recent literature that describes the role of these contractile forces and how these forces could be balanced by mitotic adhesion complexes.

摘要

分裂能力是活细胞的基本特性。细胞分裂的 3D 方向对于胚胎发生、组织的维持和结构以及控制细胞命运至关重要。人们非常关注有丝分裂纺锤体在沿着细胞最长轴放置自身的作用,在有丝分裂中心体延伸到细胞皮质的微管群体之间发生一种形状感应机制。然而,细胞皮质的收缩力也可能在决定分裂后子细胞的最终位置方面发挥决定性作用。在这篇综述中,我们讨论了最近描述这些收缩力作用的文献,以及这些力如何通过有丝分裂黏附复合物来平衡。