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中国仓鼠卵巢细胞中高温下DNA链断裂的修复

Repair of DNA strand breaks at hyperthermic temperatures in Chinese hamster ovary cells.

作者信息

Warters R L, Axtell J

机构信息

Department of Radiology, University of Utah Health Sciences Center, Salt Lake City 84132.

出版信息

Int J Radiat Biol. 1992 Jan;61(1):43-8. doi: 10.1080/09553009214550601.

Abstract

The repair of DNA double-strand breaks was measured by pH 7.2 filter elution in cells incubated at 25-45 degrees C either before or after X-irradiation. Exposure to 45 degrees C for 15 minutes immediately prior to X-irradiation significantly increased both the half-time for DNA double-strand break closure and the number of DNA double-strand breaks remaining in nuclear DNA 180 minutes after irradiation. Exposure to temperatures between 41 and 45 degrees C immediately after X-irradiation accelerated DNA double-strand break closure and resulted in no increase in the number of DNA double-strand breaks remaining in the cell's genome 180 minutes after irradiation. The results indicate either that the radiosensitization produced by the administration of hyperthermic temperatures before and after irradiation result from two characteristically different molecular mechanisms, or that neither the rate of DNA strand break closure nor the number of DNA strand breaks remaining in nuclear DNA after irradiation accurately predict hyperthermic radiosensitization. These conclusions assume that no DNA strand breaks are below the resolution of this DNA damage assay and that a comparison between cytotoxicity and DNA repair after exposure to high radiation doses is valid.

摘要

通过pH 7.2滤膜洗脱法,在X射线照射之前或之后,于25 - 45摄氏度孵育的细胞中测量DNA双链断裂的修复情况。在X射线照射前立即暴露于45摄氏度15分钟,显著增加了DNA双链断裂闭合的半衰期以及照射后180分钟核DNA中残留的DNA双链断裂数量。X射线照射后立即暴露于41至45摄氏度之间的温度下,加速了DNA双链断裂的闭合,并且在照射后180分钟细胞基因组中残留的DNA双链断裂数量没有增加。结果表明,照射前后给予高温所产生的放射增敏作用要么源于两种截然不同的分子机制,要么照射后DNA链断裂闭合的速率以及核DNA中残留的DNA链断裂数量都不能准确预测高温放射增敏作用。这些结论假定在此DNA损伤检测方法的分辨率之下不存在DNA链断裂,并且在暴露于高辐射剂量后细胞毒性与DNA修复之间的比较是有效的。

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