Wharton W
J Cell Physiol. 1983 Dec;117(3):423-9. doi: 10.1002/jcp.1041170318.
Density-arrested human fibroblasts were stimulated to traverse G0/G1 and initiate DNA synthesis by the addition of medium containing either serum or a combination of platelet-derived growth factor and platelet-poor plasma. Medium containing a combination of epidermal growth factor and high concentrations of insulin also stimulated DNA synthesis in platelet factor-treated quiescent cells. Platelet factor was required only to initiate proliferation. Epidermal growth factor and insulin then allowed G1 traverse and commitment to DNA synthesis. Cells could complete S, G2, and M in unsupplemented medium lacking peptide growth factors.
通过添加含有血清或血小板衍生生长因子与乏血小板血浆组合的培养基,刺激处于密度抑制状态的人成纤维细胞穿越G0/G1期并启动DNA合成。含有表皮生长因子和高浓度胰岛素组合的培养基也能刺激经血小板因子处理的静止细胞中的DNA合成。血小板因子仅用于启动增殖。然后,表皮生长因子和胰岛素使细胞穿越G1期并进入DNA合成阶段。细胞可以在缺乏肽生长因子的未补充培养基中完成S期、G2期和M期。