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扁桃体淋巴细胞摄取的外源DNA的命运

Fate of foreign DNA taken up by tonsillar lymphocytes.

作者信息

Ohlbaum A, Csuzi S, Medveczky P, Antoni F

出版信息

Acta Biochim Biophys Acad Sci Hung. 1977;12(1):15-23.

PMID:405837
Abstract

The uptake of heterologous (B. cereus) DNA by tonsillar lymphocytes was followed for 22 hours. Acid-precipitable DNA became associated with the cells as soon as they were mixed with DNA. The uptake was linear from 0 to 3 hours, between 3 to 6 hours part of the cell-associated DNA was released into the incubation medium, and at 22 hours the amount of label in the cells reached the values measured at 2--3 hours. In respect of the size of DNA the uptake seemed to follow the same saturation curve. There was no difference between the uptake pattern of native DNA and that of heat-denatured DNA. The decrease of size of foreign DNA in the cells in the incubation medium was followed by agarose-gel electrophoresis. In tonsillar lymphocytes enzyme activities capable of degrading heterologous DNA were found. The enzyme activities present in the cells could be detected in the culture medium as well for at least 24 hours.

摘要

对扁桃体淋巴细胞摄取异源(蜡样芽孢杆菌)DNA的情况进行了22小时的跟踪观察。一旦细胞与DNA混合,酸沉淀性DNA就会与细胞结合。摄取在0至3小时呈线性,在3至6小时期间,部分与细胞结合的DNA释放到培养液中,在22小时时,细胞中的标记量达到2至3小时时测得的值。就DNA大小而言,摄取似乎遵循相同的饱和曲线。天然DNA和热变性DNA的摄取模式没有差异。通过琼脂糖凝胶电泳跟踪培养液中细胞内异源DNA大小的减小情况。在扁桃体淋巴细胞中发现了能够降解异源DNA的酶活性。细胞中存在的酶活性在培养基中至少24小时也能被检测到。

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