Tang N, Cunningham K, Enger M D
Department of Zoology and Genetics, Iowa State University, Ames 50011.
Exp Cell Res. 1991 Sep;196(1):13-9. doi: 10.1016/0014-4827(91)90450-9.
Clonal subpopulations of NRK-49F cells were isolated and characterized for their responses to transforming growth factor beta (TGF beta). Two fibroblastic clones, N1 and N4, were found to have opposite TGF beta responses. TGF beta inhibits EGF-induced proliferation in growth-arrested, subconfluent monolayer cultures of N1 but not N4 cells. In contrast, TGF beta stimulates DNA synthesis and an increase in cell number in N4 but not N1 cells. The inhibitory effect of TGF beta on DNA synthesis in N1 cells is due not to modulation of the EGF receptor or other early G1 events. EGF-induced myc mRNA accumulation is not inhibited, and the action point for TGF beta inhibition of the entry into S of N1 cells is at the G1-S boundary.
分离出NRK - 49F细胞的克隆亚群,并对其对转化生长因子β(TGFβ)的反应进行了表征。发现两个成纤维细胞克隆N1和N4对TGFβ有相反的反应。在生长停滞、亚汇合单层培养的N1细胞中,TGFβ抑制表皮生长因子(EGF)诱导的增殖,但对N4细胞无此作用。相反,TGFβ刺激N4细胞中的DNA合成并增加细胞数量,但对N1细胞无此作用。TGFβ对N1细胞中DNA合成的抑制作用并非由于EGF受体或其他早期G1期事件的调节。EGF诱导的myc mRNA积累未受抑制,TGFβ抑制N1细胞进入S期的作用点在G1 - S边界。