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Age associated increase of single-stranded regions in the DNA of mouse brain and liver cells.

作者信息

Nakanishi K, Shima A, Fukuda M, Fujita S

出版信息

Mech Ageing Dev. 1979 May;10(3-4):273-81. doi: 10.1016/0047-6374(79)90041-1.

DOI:10.1016/0047-6374(79)90041-1
PMID:379460
Abstract

The touch smears of brain cells and hepatocytes of young and senescent mice were stained with antibody to cytidine nucleoside by an indirect immunofluorescence technique and subsequently combined with fluorescence cresyl violet staining of DNA. Nuclear binding of the antibody which reacts only with denatured or single-stranded regions in the DNA was seen only in the tissues of an aging animal. No such DNA lesion was detected in the epithelial cells of the gastrointestinal tract at any age. This type of DNA alteration is supposed to accumulate in the slowly renewing and non-replenishing tissues as a function of aging. The antibody was found not to react with the cells in S phase as demonstrated by 3H-thymidine autoradiography on a smear of newborn hepatocytes after the double fluorescence staining with cresyl violet and anti-cytidine antibody.

摘要

相似文献

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Age associated increase of single-stranded regions in the DNA of mouse brain and liver cells.
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2
Estimation of the single stranded region in the nuclear DNA of mouse tissues during aging with special reference to the brain.
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Genomic damage and its repair in young and aging brain.年轻及衰老大脑中的基因组损伤及其修复
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Quantitative detection of DNA damage in the neuronal cells of the cerebellum and cerebrum by the analysis of Feulgen hydrolysis curves.
通过福尔根水解曲线分析对小脑和大脑神经细胞中的DNA损伤进行定量检测。
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