Balin A K, Goodman D B, Rasmussen H, Cristofalo V J
J Cell Biol. 1978 Aug;78(2):390-400. doi: 10.1083/jcb.78.2.390.
We had established that growth of human diploid WI-38 cells is reversibly inhibited by elevated partial pressures of oxygen (PO2) and we were interested in determining where in the cell cycle growth was delayed. A technique combining cytospectrophotometry and autoradiography was used to determine cell cycle parameters. Confluent cells that were subcultivated and exposed to a PO2 of 365 +/- 8 mm Hg were delayed primarily after DNA synthesis but before metaphase. At a PO2 of 590 +/- 35 mm Hg, most cells did not initiate DNA synthesis, and the few that did, failed to complete the process. When exponentially growing cells that had already begun DNA synthesis were exposed to a PO2 of 590 p 35 mm Hg, they accumulated after completing DNA synthesis but before initiating mitosis. The rate at which (3H)thymidine was incorporated into DNA was inversely correlated with oxygen tension (PO2 of 135--590 mm Hg). These results suggest that the process most sensitive to oxygen causes cells to be delayed after DNA synthesis but before metaphase. Slightly higher PO2's were needed to inhibit the initiation of DNA synthesis. Further, the rate of DNA synthesis is decreased by elevated oxygen tensions.
我们已经确定,人二倍体WI-38细胞的生长会受到氧分压(PO2)升高的可逆抑制,并且我们有兴趣确定细胞周期中的生长延迟发生在何处。一种结合细胞分光光度法和放射自显影术的技术被用于确定细胞周期参数。传代培养并暴露于365±8 mmHg的PO2的汇合细胞主要在DNA合成后但在中期之前出现延迟。在590±35 mmHg的PO2下,大多数细胞未启动DNA合成,而少数启动的细胞也未能完成该过程。当已经开始DNA合成的指数生长细胞暴露于590±35 mmHg的PO2时,它们在完成DNA合成后但在启动有丝分裂之前积累。(3H)胸腺嘧啶核苷掺入DNA的速率与氧张力(135 - 590 mmHg的PO2)呈负相关。这些结果表明,对氧最敏感的过程会使细胞在DNA合成后但在中期之前出现延迟。抑制DNA合成的起始需要略高的PO2。此外,升高的氧张力会降低DNA合成的速率。