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利用低温使人类二倍体成纤维细胞生长停滞并同步化。

Use of low temperature for growth arrest and synchronization of human diploid fibroblasts.

作者信息

Enninga I C, Groenendijk R T, van Zeeland A A, Simons J W

出版信息

Mutat Res. 1984 Oct;130(5):343-52. doi: 10.1016/0165-1161(84)90020-7.

Abstract

The growth kinetics of human diploid fibroblasts at two different temperatures were followed. Proliferation of exponentially growing cells is reduced and eventually stops upon incubation at low temperature (i.e. 30 degrees C). The cells which are in S phase at the time of switching to low temperature complete their DNA synthesis and become arrested in the G1 phase of the cell cycle. The arrested cells can be stimulated to proliferate by restoration of the optimal growth temperature (37 degrees C). The kinetics of entry into S phase were investigated by measuring [3H]thymidine incorporation into TCA-precipitable material, by autoradiography and by flow cytofluorimetry. The synchronized cells initiate DNA synthesis at approximately 8 h and DNA synthesis peaks at 20.4 +/- 0.7 h after stimulation. In addition, the rates of UV-induced excision repair at 30 degrees C and 37 degrees C were compared. The results indicate that at 30 degrees C the excision-repair process is operative but at a slightly reduced rate in comparison with repair at 37 degrees C. This method will be useful for the study of S-phase-dependent processes, as well as for repair studies in the absence of cell division.

摘要

对人二倍体成纤维细胞在两种不同温度下的生长动力学进行了跟踪研究。指数生长的细胞在低温(即30℃)培养时增殖减少,最终停止。在切换到低温时处于S期的细胞完成其DNA合成,并停滞在细胞周期的G1期。通过恢复最佳生长温度(37℃),可以刺激停滞的细胞增殖。通过测量[3H]胸腺嘧啶核苷掺入三氯乙酸可沉淀物质、放射自显影和流式细胞荧光术来研究进入S期的动力学。同步化的细胞在刺激后约8小时开始DNA合成,DNA合成在20.4±0.7小时达到峰值。此外,还比较了30℃和37℃下紫外线诱导的切除修复率。结果表明,在30℃时切除修复过程是有效的,但与37℃下的修复相比,速率略有降低。该方法将有助于研究S期依赖性过程,以及在无细胞分裂情况下的修复研究。

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