Little J B, Ueno A M, Dahlberg W K
Laboratory of Radiobiology, Harvard School of Public Health, Boston, MA 02115.
Radiat Environ Biophys. 1989;28(3):193-202. doi: 10.1007/BF01211256.
We have examined the effects of several classes of metabolic inhibitors on the repair of potentially lethal damage in density-inhibited cultures of two rodent and two human cell systems which differ in their growth characteristics. Aphidicolin, 1-beta-D-arabinofuranosylcytosine (ara-C) and hydroxyurea showed no effect on PLD repair, whereas the effects of 9-beta-D-arabinofuranosyladenine (ara-A) and 3-aminobenzamide (3-AB) were cell line dependent. For example, 3-AB suppressed PLD repair almost completely in CHO cells, but showed no inhibitory effects in human diploid fibroblasts. These results indicate that inhibitors of DNA replication and poly(ADP-ribose) synthesis are not efficient inhibitors of cellular recovery in irradiated cells and, moreover, that such effects may be cell line dependent.
我们研究了几类代谢抑制剂对两种啮齿动物和两种人类细胞系统的密度抑制培养物中潜在致死损伤修复的影响,这些细胞系统在生长特性上有所不同。阿非科林、1-β-D-阿拉伯呋喃糖基胞嘧啶(ara-C)和羟基脲对潜在致死损伤修复没有影响,而9-β-D-阿拉伯呋喃糖基腺嘌呤(ara-A)和3-氨基苯甲酰胺(3-AB)的影响则取决于细胞系。例如,3-AB几乎完全抑制了CHO细胞中的潜在致死损伤修复,但对人二倍体成纤维细胞没有抑制作用。这些结果表明,DNA复制抑制剂和聚(ADP-核糖)合成抑制剂不是受照射细胞中细胞恢复的有效抑制剂,此外,这种影响可能取决于细胞系。