Suppr超能文献

兔脾外植体中的DNA合成及其与细胞分裂的关系。

DNA synthesis in rabbit spleen explants. Its relationship to cell division.

作者信息

Harris G, Olsen I, Marriott P

出版信息

Immunology. 1975 Oct;29(4):687-96.

Abstract

The synthesis of DNA, as measured by the incorporation of [3H]-thymidine into the nuclei of cells of cultured explants of rabbit spleen, has been studied and correlated with estimation of DNA content of these nuclei using Feulgen densitometry, with and without colcemid arrest. Observations of the proportion of nuclei labelled with [3H]thymidine and their DNA content indicated that many cells were incorporating this precursor for DNA synthesis without the concomitant increases in DNA expected of cells in division cycle. Colcemid arrest failed to produce the changes in DNA content expected of a cell population as rapidly dividing as the labelling kinetics suggested. The results indicated that [3H]thymidine-labelled material, possibly DNA, was being transferred between cells and this accounted for the increased labelling index seen after pulsing with [3H]thymidine. The suppression of [3H]thymidine uptake by hydroxyurea indicated that this was not repair synthesis of damaged DNA.

摘要

通过将[3H] - 胸苷掺入兔脾脏培养外植体细胞的细胞核中来测量DNA的合成,并与使用福尔根密度测定法估计这些细胞核的DNA含量相关联,同时研究了有无秋水仙酰胺阻断的情况。观察用[3H] - 胸苷标记的细胞核比例及其DNA含量表明,许多细胞正在掺入这种用于DNA合成的前体,而没有出现处于分裂周期的细胞预期的DNA相应增加。秋水仙酰胺阻断未能像标记动力学所表明的那样,使细胞群体的DNA含量产生预期的快速分裂变化。结果表明,[3H] - 胸苷标记的物质(可能是DNA)正在细胞间转移,这解释了用[3H] - 胸苷脉冲后观察到的标记指数增加。羟基脲对[3H] - 胸苷摄取的抑制表明,这不是受损DNA的修复合成。

相似文献

3
In vitro stimulation by tumour cell media of [3H]-thymidine incorporation by mouse spleen lymphocytes.
Cell Biochem Funct. 1997 Jun;15(2):119-26. doi: 10.1002/(SICI)1099-0844(19970601)15:2<119::AID-CBF731>3.0.CO;2-C.
7
Autoradiographic studies of DNA synthesis in lymphoid tissues.
J Microsc. 1976 Mar;106(2):173-84. doi: 10.1111/j.1365-2818.1976.tb02399.x.

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验