Abelson H T, Antoniades H N, Scher C D
Biochim Biophys Acta. 1979 Feb 27;561(2):269-75. doi: 10.1016/0005-2787(79)90136-9.
The addition of whole serum to G0-arrested, confluent Balb/c-3T3 cells induces them to progress through G1 and synthesize DNA after a 12-h lag period. Prior to the onset of DNA synthesis, RNA is synthesized and RNA content increases. Serum has been fractionated into two sets of growth factors: a platelet-derived growth factor present in heat-treated (100 degrees C) platelet extracts and platelet-poor plasma. Addition of whole serum, platelet-derived growth factor or platelet-poor plasma induces quiescent cells to increase their cytoplasmic RNA content, but the cells treated with platelet-poor plasma do not synthesize DNA. Messenger RNA content increases within 2 h after stimulation with whole serum or platelet-poor plasma, and after 18 h, mRNA has accumulated to a greater degree than rRNA.
向处于G0期停滞、汇合的Balb/c-3T3细胞中添加全血清,会使其在延迟12小时后进入G1期并合成DNA。在DNA合成开始之前,会先合成RNA且RNA含量增加。血清已被分离成两组生长因子:存在于热处理(100摄氏度)血小板提取物和贫血小板血浆中的血小板衍生生长因子。添加全血清、血小板衍生生长因子或贫血小板血浆会诱导静止细胞增加其细胞质RNA含量,但用贫血小板血浆处理的细胞不会合成DNA。在用全血清或贫血小板血浆刺激后2小时内,信使RNA含量增加,18小时后,mRNA积累的程度比rRNA更大。