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光解型钙黏蛋白通过光抑制细胞间力学转导。

Photocleavable Cadherin Inhibits Cell-to-Cell Mechanotransduction by Light.

机构信息

Department of Chemistry, Graduate School of Science , The University of Tokyo , 7-3-1 Hongo , Bunkyo-ku, Tokyo 113-0033 , Japan.

出版信息

ACS Chem Biol. 2019 Oct 18;14(10):2206-2214. doi: 10.1021/acschembio.9b00460. Epub 2019 Sep 20.

DOI:10.1021/acschembio.9b00460
PMID:31503442
Abstract

Precise integration of individual cell behaviors is indispensable for collective tissue morphogenesis and maintenance of tissue integrity. Organized multicellular behavior is achieved mechanical coupling of individual cellular contractility, mediated by cell adhesion molecules at the cell-cell interface. Conventionally, gene depletion or laser microsurgery has been used for functional analysis of intercellular mechanotransduction. Nevertheless, these methods are insufficient to investigate either the spatiotemporal dynamics or the biomolecular contribution in cell-cell mechanical coupling within collective multicellular behaviors. Herein, we present our effort in adaption of PhoCl for attenuation of cell-to-cell tension transmission mediated by E-cadherin. To release intercellular contractile tension applied on E-cadherin molecules with external light, a genetically encoded photocleavable module called PhoCl was inserted into the intracellular domain of E-cadherin, thereby creating photocleavable cadherin (PC-cadherin). In response to light illumination, the PC-cadherin cleaved into two fragments inside cells, resulting in attenuating mechanotransduction at intercellular junctions in living epithelial cells. Light-induced perturbation of the intercellular tension balance with surrounding cells changed the cell shape in an epithelial cell sheet. The method is expected to enable optical manipulation of force-mediated cell-to-cell communications in various multicellular behaviors, which contributes to a deeper understanding of embryogenesis and oncogenesis.

摘要

精确整合单个细胞的行为对于组织形态发生和组织完整性的维持是不可或缺的。有组织的多细胞行为是通过细胞间的黏附分子在细胞-细胞界面实现的单个细胞收缩的机械偶联。传统上,基因耗竭或激光显微手术已被用于细胞间力学转导的功能分析。然而,这些方法不足以研究集体多细胞行为中细胞-细胞机械偶联的时空动态或生物分子贡献。在这里,我们介绍了我们在适应 PhoCl 以衰减由 E-钙黏蛋白介导的细胞间张力传递方面的努力。为了用光释放作用于 E-钙黏蛋白分子的细胞间收缩张力,我们将一种称为 PhoCl 的遗传编码光可裂解模块插入 E-钙黏蛋白的细胞内结构域,从而创建光可裂解钙黏蛋白(PC-钙黏蛋白)。对光的响应,PC-钙黏蛋白在细胞内裂解成两个片段,从而减弱活上皮细胞中细胞间连接的力学转导。与周围细胞的光诱导的细胞间张力平衡的扰动改变了上皮细胞层中的细胞形状。该方法有望实现对各种多细胞行为中力介导的细胞间通讯的光操纵,这有助于深入理解胚胎发生和肿瘤发生。

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