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DNA释放作为吞噬细胞杀灭微生物的直接衡量指标。

DNA release as a direct measure of microbial killing by phagocytes.

作者信息

Friedlander A M

出版信息

Infect Immun. 1978 Oct;22(1):148-54. doi: 10.1128/iai.22.1.148-154.1978.

Abstract

A new assay for the precise measurement of microbial killing by leukocytes is presented. The method assumes that release of radioactively labeled DNA from the microbe is direct evidence of cell death. Human peripheral blood leukocytes incubated with [14C]thymidine-labeled Salmonella typhimurium released 32 to 59% of the radioactivity after 4 h and 63 to 75% after 18 h. Inactivated leukocytes released less than 5% of the radioactivity. None of the released radioactivity is retained within the leukocyte, and 60% remains precipitable with trichloroacetic acid. Leukocytes released substantial radioactivity from labeled Escherichia coli but only a slight amount from staphylococci. Mouse peritoneal macrophages were also shown to release radioactivity from Salmonella. The DNA release assay avoids the errors inherent in prior killing methods which measure viability by growth inhibition. It is rapid, reproducible, and highly specific.

摘要

本文介绍了一种用于精确测量白细胞杀灭微生物的新检测方法。该方法假定从微生物中释放出放射性标记的DNA是细胞死亡的直接证据。用人外周血白细胞与[14C]胸苷标记的鼠伤寒沙门氏菌一起孵育,4小时后释放出32%至59%的放射性,18小时后释放出63%至75%。灭活的白细胞释放出的放射性小于5%。释放出的放射性没有保留在白细胞内,60%仍可被三氯乙酸沉淀。白细胞从标记的大肠杆菌中释放出大量放射性,但从葡萄球菌中仅释放出少量放射性。还显示小鼠腹腔巨噬细胞从沙门氏菌中释放出放射性。DNA释放检测避免了先前通过生长抑制测量活力的杀灭方法中固有的误差。它快速、可重复且高度特异。

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本文引用的文献

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H3-thymidine and the conservation of deoxyribonucleic acid.H3-胸苷与脱氧核糖核酸的保守性
J Bacteriol. 1966 Dec;92(6):1840-1. doi: 10.1128/jb.92.6.1840-1841.1966.

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