Leof E B, Van Wyk J J, O'Keefe E J, Pledger W J
Exp Cell Res. 1983 Aug;147(1):202-8. doi: 10.1016/0014-4827(83)90285-9.
Density-arrested BALB/c-3T3 cells that had received a transient exposure to PDGF and were then transferred to medium containing only EGF and somatomedin C (Sm-C) began DNA synthesis after the G0/G1 lag. Supraphysiological concentrations of insulin could be employed to replace the Sm-C requirement. This G0/G1 lag phase was bisected by the requirement for the exogenous presence of EGF. Our data indicated that EGF was required during the traverse of only the first half of G0/G1 phase (6 h) and not during the traverse of late G1. Subphysiological serum concentrations of Sm-C were also necessary to be present with EGF for progression through early G0/G1; however, traverse of the final half of G0/G1 and commitment to DNA synthesis required the presence of Sm-C. It was found that physiological concentrations of Sm-C were required for the traverse late G1. The requirement for Sm-C for G0/G1 traverse of BALB/c-3T3 cells as opposed to human fibroblasts or glial cells may be due to a difference in endogenous synthesis of an insulin-like growth factor. Our data are in close agreement with previous reports that EGF is only required for approximately the first 8 h during traverse of the G0/G1 phase. The requirement for EGF to be present for the first 6 h of G0/G1 could result from a continued or repetitious event or by more than one distinct EGF-requiring event.
短暂暴露于血小板源性生长因子(PDGF)后,再转移至仅含表皮生长因子(EGF)和生长调节素C(Sm-C)的培养基中的密度抑制BALB/c-3T3细胞,在G0/G1期停滞之后开始DNA合成。超生理浓度的胰岛素可用于替代对Sm-C的需求。这种G0/G1期停滞阶段被对外源性EGF存在的需求一分为二。我们的数据表明,EGF仅在G0/G1期的前半段(6小时)穿越过程中是必需的,而在G1晚期穿越过程中则不是必需的。亚生理血清浓度的Sm-C也必须与EGF同时存在,以便细胞通过G0/G1早期;然而,G0/G1期后半段的穿越以及对DNA合成的启动需要Sm-C的存在。研究发现,生理浓度的Sm-C是G1晚期穿越所必需的。与人类成纤维细胞或神经胶质细胞相比,BALB/c-3T3细胞在G0/G1期穿越过程中对Sm-C的需求差异,可能是由于胰岛素样生长因子内源性合成的差异所致。我们的数据与之前的报道密切一致,即EGF仅在G0/G1期穿越的大约前8小时是必需的。在G0/G1期的前6小时需要EGF存在,可能是由于持续或重复的事件,或者是由不止一个不同的需要EGF的事件导致的。