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细胞-细胞连接完整性对 MDCK II 细胞汇合力学的重要性。

Importance of integrity of cell-cell junctions for the mechanics of confluent MDCK II cells.

机构信息

University of Goettingen, Institute of Physical Chemistry, Tammannstr. 6, 37077, Goettingen, Germany.

出版信息

Sci Rep. 2018 Sep 20;8(1):14117. doi: 10.1038/s41598-018-32421-2.

Abstract

Intercellular junctions are important mechanical couplers between cells in epithelial layers providing adhesion and intercellular communication. Regulation of the junctions occurs in cellular processes such as layer formation, epithelial-to-mesenchymal transition, embryogenesis, and cancer progression. Many studies addressed the role of force generation in cells for establishing lateral cell-cell junctions and the role of cellular force transmission in tissue formation and maintenance. Our atomic force microscopy- (AFM) based study shed light on the role of both, tight junctions and adherens junctions for the mechanical properties of individual epithelial cells that are part of a confluent monolayer. We found that tight junctions are important for the establishment of a functional barrier-forming layer but impairing them does not reduce the mechanical integrity of cells. Depletion of ZO-1 results in a weak increase in cortical tension. An opposite effect was observed for disruption of E-cadherin-mediated adherens junctions using DTT. Opening of adherens junctions leads to substantial alterations of cellular mechanics such as reduced overall stiffness, but these changes turned out to be reversible after re-establishing disulfide bridges in E-cadherin by removal of DTT. We found that regulatory mechanisms exist that preserve mechanical integrity during recovery of disrupted adherens junctions.

摘要

细胞间连接是上皮细胞层中细胞间重要的力学偶联物,提供细胞间的黏附和通讯。连接的调节发生在细胞过程中,如层形成、上皮-间充质转化、胚胎发生和癌症进展。许多研究都探讨了力生成在建立侧向细胞-细胞连接中的作用,以及细胞力传递在组织形成和维持中的作用。我们的原子力显微镜(AFM)研究揭示了紧密连接和黏附连接在组成融合单层的单个上皮细胞的力学特性中的作用。我们发现,紧密连接对于建立功能性屏障形成层很重要,但破坏它们不会降低细胞的力学完整性。ZO-1 的耗竭会导致皮质张力微弱增加。用 DTT 破坏 E-钙黏蛋白介导的黏附连接会产生相反的效果。黏附连接的打开会导致细胞力学的显著改变,例如整体刚度降低,但在用 DTT 去除 E-钙黏蛋白中的二硫键重新建立后,这些变化被证明是可逆的。我们发现,在恢复破坏的黏附连接时,存在维持力学完整性的调节机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2f8/6148251/6cc8205ecf29/41598_2018_32421_Fig1_HTML.jpg

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