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[NIH 3T3细胞进入DNA合成期对其前期静止状态持续时间的依赖性]

[Dependence of the entry of NIH 3T3 cells into a period of DNA synthesis on the duration of their preliminary resting state].

作者信息

Setkov N A, Polunovskiĭ V A, Epifanova O I

出版信息

Tsitologiia. 1984 Aug;26(8):936-41.

PMID:6495396
Abstract

Using radioautography and cell fusion technique, we studied cell kinetics and functional properties of NIH 3T3 mouse fibroblasts stimulated to proliferate after being quiescent for 3, 7 and 14 days. The resting state was achieved by cultivating cells in the medium with 0.5% of serum, the stimulation being achieved by replacement of the depleted medium for a fresh one containing 10% of serum. It was found that the longer cells had been kept resting, the longer their prereplicative period lasted after the stimulation, the lesser was the fraction of cells that entered the S-period. Cell-fusion experiments revealed that the ability of the resting nuclei to suppress the onset of DNA synthesis in the nuclei of stimulated cells in heterodikaryons increased as the cells stayed in the resting state before fusion, and that the period of suppression was prolonged. The data are consistent with the idea of cells going into deeper resting states. It may be concluded that the resting cells undergo a gradual development resulting in the changes of their functional properties.

摘要

利用放射自显影术和细胞融合技术,我们研究了静息3、7和14天后被刺激增殖的NIH 3T3小鼠成纤维细胞的细胞动力学和功能特性。通过在含0.5%血清的培养基中培养细胞来实现静息状态,通过用含10%血清的新鲜培养基替换耗尽的培养基来实现刺激。结果发现,细胞静息的时间越长,刺激后其复制前期持续的时间就越长,进入S期的细胞比例就越小。细胞融合实验表明,静息细胞核抑制异核体中受刺激细胞核DNA合成起始的能力随着融合前细胞处于静息状态的时间延长而增强,且抑制期延长。这些数据与细胞进入更深静息状态的观点一致。可以得出结论,静息细胞经历了一个逐渐发展的过程,导致其功能特性发生变化。

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