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刃天青还原作为牛中性粒细胞呼吸爆发的一项功能。

Resazurin reduction as a function of respiratory burst in bovine neutrophils.

作者信息

Fang W, Myllys V, Sandholm M

机构信息

Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Helsinki, Finland.

出版信息

Am J Vet Res. 1997 Jun;58(6):601-7.

PMID:9185965
Abstract

OBJECTIVE

To determine whether the respiratory burst of neutrophils from bovine blood and milk can be analyzed by use of a fluorometric resazurin reduction assay.

SAMPLE POPULATION

Neutrophils were obtained from EDTA-anticoagulated blood of 7 dairy cows. Neutrophils also were isolated from milk samples of a cow intramammarily challenge exposed with Escherichia coli lipopolysaccharide.

PROCEDURE

The respiratory burst of neutrophils was analyzed in parallel, using the conventional luminol-enhanced luminometric procedure and a novel fluorometric procedure with resazurin as the fluorogenic substrate. Opsonized zymosan and phorbol myristate acetate were used as stimulants. The mechanism of the fluorescent response was analyzed, using metabolic inhibitors to various cell functions. Luminometry and fluorometry were carried out in parallel, using microtitration tray-reading instruments.

RESULTS

Stimulation of neutrophils induced resazurin reduction to resorufin and a fluorescent response. The luminescent response was transient, but the fluorescent response (build-up of fluorescent resorufin) was cumulative. Therefore, a single end-point measurement can be used for the fluorometric assay.

CONCLUSIONS

The proposed fluorometric microtitration tray technology is simple and has a high throughput capacity. The fluorometric and luminometric assays seem to have similar potential in the analysis of phagocyte functions.

摘要

目的

确定是否可以使用荧光刃天青还原试验分析来自牛血和牛奶的中性粒细胞的呼吸爆发。

样本群体

从7头奶牛的乙二胺四乙酸(EDTA)抗凝血液中获取中性粒细胞。中性粒细胞也从一头经乳房内注射大肠杆菌脂多糖激发的奶牛的牛奶样本中分离得到。

程序

使用传统的鲁米诺增强发光法和以刃天青作为荧光底物的新型荧光法并行分析中性粒细胞的呼吸爆发。用调理酵母聚糖和佛波酯作为刺激物。使用针对各种细胞功能的代谢抑制剂分析荧光反应的机制。使用微量滴定板读数仪器并行进行发光测定和荧光测定。

结果

中性粒细胞的刺激导致刃天青还原为试卤灵并产生荧光反应。发光反应是短暂的,但荧光反应(荧光试卤灵的积累)是累积性的。因此,荧光测定可采用单一终点测量。

结论

所提出的荧光微量滴定板技术简单且具有高通量能力。荧光测定法和发光测定法在吞噬细胞功能分析中似乎具有相似的潜力。

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