Fedor-Chaiken Mary, Hein Patrick W, Stewart Jane C, Brackenbury Robert, Kinch Michael S
Department of Cell Biology, Neurobiology, and Anatomy, University of Cincinnati College of Medicine, Cincinnati, OH 45267-0521, USA.
Cell Commun Adhes. 2003 Mar-Apr;10(2):105-18.
We found that E-cadherin and epidermal growth factor receptor (EGFR) are associated in mammary epithelial cells and that E-cadherin engagement in these cells induces transient activation of EGFR, as previously seen in keratinocytes (37). In contrast, EGFR does not associate with and is not activated by N-cadherin. Analysis of cells expressing chimeric cadherins revealed that the extracellular domain of E-cadherin is required for interaction with and activation of EGFR. This activation results in tyrosine phosphorylation of known EGFR substrates and reduction in focal adhesions. These interactions, however, are not necessary for suppression of cell motility by E-cadherin.
我们发现,E-钙黏蛋白与乳腺上皮细胞中的表皮生长因子受体(EGFR)相关联,并且这些细胞中E-钙黏蛋白的结合会诱导EGFR的瞬时激活,正如之前在角质形成细胞中所观察到的那样(37)。相比之下,EGFR不与N-钙黏蛋白相关联,也不会被N-钙黏蛋白激活。对表达嵌合钙黏蛋白的细胞进行分析发现,E-钙黏蛋白的细胞外结构域是与EGFR相互作用并激活EGFR所必需的。这种激活导致已知EGFR底物的酪氨酸磷酸化,并减少粘着斑。然而,这些相互作用对于E-钙黏蛋白抑制细胞运动并非必需。