Hamilton T A, Fishman M, Crawford G, Look A T
Cell Immunol. 1983 Apr 15;77(2):233-41. doi: 10.1016/0008-8749(83)90024-2.
Recent work has shown that macrophage-mediated cytostatic activity inhibits cell cycle traverse in G1 and/or S phase of the cell cycle without affecting late S, G2, or M phases. The present report is directed at distinguishing between such cytostatic effects on G1 phase or S phase using the accumulation of DNA polymerase alpha as a marker of G1 to S phase transition. Quiescent lymphocytes stimulated with concanavalin A undergo a semisynchronous progression from G0 to G1 to S phase with a dramatic increase in DNA polymerase alpha activity between 20 and 30 hr after stimulation. This increase in enzyme activity was inhibited, as was the accumulation of DNA, when such cells were cocultured with activated murine peritoneal macrophages during this time interval. However, if mitogen-stimulated lymphocytes were enriched for S-phase cells by centrifugal elutriation and cocultured with activated macrophages for 4-6 hr, DNA synthesis was inhibited but the already elevated DNA-polymerase activity was unaffected. Similar results were obtained when a virally transformed lymphoma cell line was substituted as the target cell in this assay. These results show that both G1 and S phase of the cycle are inhibited and suggest that inhibition of progression through the different phases may be accomplished by at least two distinct mechanisms.
最近的研究表明,巨噬细胞介导的细胞抑制活性可抑制细胞周期在G1期和/或S期的进程,而不影响S期后期、G2期或M期。本报告旨在通过使用DNA聚合酶α的积累作为G1期到S期转变的标志物,来区分对G1期或S期的这种细胞抑制作用。用伴刀豆球蛋白A刺激静止淋巴细胞,它们会经历从G0期到G1期再到S期的半同步进程,在刺激后20至30小时之间,DNA聚合酶α活性会急剧增加。当这些细胞在此时间间隔内与活化的小鼠腹腔巨噬细胞共培养时,酶活性的增加受到抑制,DNA的积累也受到抑制。然而,如果通过离心淘洗将有丝分裂原刺激的淋巴细胞富集为S期细胞,并与活化的巨噬细胞共培养4至6小时,DNA合成受到抑制,但已经升高的DNA聚合酶活性不受影响。当在该试验中用病毒转化的淋巴瘤细胞系替代靶细胞时,也获得了类似的结果。这些结果表明,细胞周期的G1期和S期均受到抑制,并表明通过不同阶段的进程抑制可能是由至少两种不同的机制完成的。