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DNA损伤剂诱导静止期人成纤维细胞进行复制性DNA合成。

Induction of replicative DNA synthesis in quiescent human fibroblasts by DNA damaging agents.

作者信息

Cohn S M, Krawisz B R, Dresler S L, Lieberman M W

出版信息

Proc Natl Acad Sci U S A. 1984 Aug;81(15):4828-32. doi: 10.1073/pnas.81.15.4828.

Abstract

A marked induction of DNA replication was observed in confluent human diploid fibroblast cultures treated with low relatively nontoxic doses of UV radiation, N-methyl-N-nitrosourea (MNU), and N-acetoxy-2-acetylaminofluorene (AAAF). Isopycnic CsCl density gradient analysis of newly synthesized DNA labeled with BrdUrd indicated that most of the synthesis was semiconservative. The rate of semiconservative DNA synthesis was maximal 24 hr after damage. This induction of DNA replication was greatest at approximately equal to 3 J/m2 UV, 0.5 mM MNU, or 1.0 microM AAAF; was inhibited by hydroxyurea and aphidicolin; and also occurred in repair-deficient xeroderma pigmentosum fibroblasts. Autoradiographic examination of both confluent cultures and serum-arrested cultures showed a large increase in the fraction of densely labeled (S phase) cells after UV treatment. These densely labeled cells retain the capacity for cell division and subsequent proliferation. We conclude that low doses of at least three different DNA damaging agents are capable of recruiting quiescent cells into a state of DNA replication similar to that observed in the normal cell cycle.

摘要

在用相对低毒剂量的紫外线辐射、N-甲基-N-亚硝基脲(MNU)和N-乙酰氧基-2-乙酰氨基芴(AAAF)处理汇合的人二倍体成纤维细胞培养物时,观察到DNA复制有明显诱导。用溴脱氧尿苷(BrdUrd)标记新合成DNA的等密度氯化铯密度梯度分析表明,大部分合成是半保留性的。半保留性DNA合成速率在损伤后24小时达到最大值。这种DNA复制诱导在约3 J/m2紫外线、0.5 mM MNU或1.0 μM AAAF时最大;被羟基脲和阿非迪霉素抑制;并且也发生在DNA修复缺陷的着色性干皮病成纤维细胞中。对汇合培养物和血清阻滞培养物的放射自显影检查显示,紫外线处理后,密集标记(S期)细胞的比例大幅增加。这些密集标记的细胞保留了细胞分裂和随后增殖的能力。我们得出结论,低剂量的至少三种不同的DNA损伤剂能够使静止细胞进入一种类似于正常细胞周期中观察到的DNA复制状态。

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