Levenberg S, Yarden A, Kam Z, Geiger B
Department of Molecular Cell Biology, The Weizmann Institute of Science, Rehovot, Israel.
Oncogene. 1999 Jan 28;18(4):869-76. doi: 10.1038/sj.onc.1202396.
In this study the direct involvement of cadherins in adhesion-mediated growth inhibition was investigated. It is shown here that overexpression of N-cadherin in CHO cells significantly suppresses their growth rate. Interaction of these cells and two additional fibroblastic lines with synthetic beads coated with N-cadherin ligands (recombinant N-cadherin ectodomain or specific antibodies) leads to growth arrest at the G1 phase of the cell cycle. The cadherin-reactive beads inhibit the entry into S phase and the reduction in the levels of cyclin-dependent kinase (cdk) inhibitors p21 and p27, following serum-stimulation of starved cells. In exponentially growing cells these beads induce G1 arrest accompanied by elevation in p27 only. We propose that cadherin-mediated signaling is involved in contact inhibition of growth by inducing cell cycle arrest at the G1 phase and elevation of p27 levels.
在本研究中,对钙黏着蛋白在黏附介导的生长抑制中的直接作用进行了研究。结果表明,在CHO细胞中过表达N-钙黏着蛋白可显著抑制其生长速率。这些细胞以及另外两条成纤维细胞系与包被有N-钙黏着蛋白配体(重组N-钙黏着蛋白胞外结构域或特异性抗体)的合成微珠相互作用,会导致细胞周期在G1期停滞。钙黏着蛋白反应性微珠抑制饥饿细胞血清刺激后进入S期以及细胞周期蛋白依赖性激酶(cdk)抑制剂p21和p27水平的降低。在指数生长的细胞中,这些微珠仅诱导G1期停滞并伴有p27水平升高。我们提出,钙黏着蛋白介导的信号传导通过诱导细胞周期在G1期停滞和p27水平升高参与生长的接触抑制。