Sherline P, Mascardo R N
Exp Cell Res. 1984 Jul;153(1):109-20. doi: 10.1016/0014-4827(84)90453-1.
We have tested the effects of various mitogens and growth inhibitors on centrosomal separation (CS) in serum-deprived HeLa, gerbil fibroma (GF) and A431 cells. All of the agents which were mitogenic in a given cell type also stimulated CS. No agent was found which stimulated CS but failed to stimulate DNA synthesis. Inhibitors of DNA synthesis, including somatostatin, hydrocortisone, 8-bromo-cAMP, and epidermal growth factor (EGF) in A431 cells, also inhibited CS in response to mitogens. In GF cells (blocked at the G1/S interface with hydroxyurea) centrosomal re-association and the decay in commitment to DNA synthesis upon serum withdrawal occurred with a similar t1/2 (8.8 h). These results demonstrate that CS and DNA synthesis are co-ordinately regulated by a variety of stimulators and inhibitors of cell proliferation. Separation of the centrosomes, or an underlying event with which it is tightly coupled, may represent the point of cellular commitment to enter S phase.
我们已经测试了多种促有丝分裂原和生长抑制剂对血清饥饿的HeLa细胞、沙鼠纤维瘤(GF)细胞和A431细胞中心体分离(CS)的影响。在给定细胞类型中具有促有丝分裂作用的所有试剂也能刺激中心体分离。未发现有试剂能刺激中心体分离但不刺激DNA合成。DNA合成抑制剂,包括生长抑素、氢化可的松、8-溴环磷酸腺苷以及A431细胞中的表皮生长因子(EGF),也能抑制对促有丝分裂原的中心体分离反应。在GF细胞中(用羟基脲阻断在G1/S界面),血清撤出后中心体重组以及对DNA合成的承诺衰减以相似的半衰期(8.8小时)发生。这些结果表明,中心体分离和DNA合成受多种细胞增殖刺激剂和抑制剂的协同调节。中心体的分离,或与之紧密相关的潜在事件,可能代表细胞进入S期的承诺点。