Mayo Clinic, Department of Biochemistry and Molecular Biology and the Miles and Shirley Fiterman Center for Digestive Diseases, Rochester, MN 55905, USA.
Mol Biol Cell. 2009 Oct;20(19):4140-52. doi: 10.1091/mbc.e08-10-1043. Epub 2009 Jul 29.
Remodeling of cell-cell contacts through the internalization of adherens junction proteins is an important event during both normal development and the process of tumor cell metastasis. Here we show that the integrity of tumor cell-cell contacts is disrupted after epidermal growth factor (EGF) stimulation through caveolae-mediated endocytosis of the adherens junction protein E-cadherin. Caveolin-1 and E-cadherin closely associated at cell borders and in internalized structures upon stimulation with EGF. Furthermore, preventing caveolae assembly through reduction of caveolin-1 protein or expression of a caveolin-1 tyrosine phospho-mutant resulted in the accumulation of E-cadherin at cell borders and the formation of tightly adherent cells. Most striking was the fact that exogenous expression of caveolin-1 in tumor cells that contain tight, well-defined, borders resulted in a dramatic dispersal of these cells. Together, these findings provide new insights into how cells might disassemble cell-cell contacts to help mediate the remodeling of adherens junctions, and tumor cell metastasis and invasion.
细胞-细胞接触的重塑是正常发育和肿瘤细胞转移过程中的一个重要事件,通过细胞内吞作用内化黏着连接蛋白来实现。在这里,我们发现表皮生长因子(EGF)刺激后,通过小窝介导的黏着连接蛋白 E-钙黏蛋白内化,破坏了肿瘤细胞-细胞接触的完整性。刺激后,细胞边缘和内化结构中紧密相关的小窝蛋白 1 和 E-钙黏蛋白。此外,通过减少小窝蛋白 1 蛋白或表达小窝蛋白 1 酪氨酸磷酸化突变体来阻止小窝组装,导致 E-钙黏蛋白在细胞边缘积累,并形成紧密黏附的细胞。最引人注目的是,在含有紧密、明确边界的肿瘤细胞中外源表达小窝蛋白 1 会导致这些细胞的明显分散。总之,这些发现为细胞如何分解细胞-细胞接触以帮助介导黏着连接的重塑以及肿瘤细胞转移和侵袭提供了新的见解。