Kampen Annette H, Tollersrud Tore, Lund Arve
Department of Animal Health, National Veterinary Institute, Oslo, Norway.
J Immunol Methods. 2004 Jun;289(1-2):47-55. doi: 10.1016/j.jim.2004.03.008.
A rapid and simple method for measurement of respiratory burst in neutrophil granulocytes in whole bovine blood is described. The respiratory burst was stimulated by live Staphylococcus aureus, and the production of reactive oxygen species quantified by the conversion of intracellular dihydrorhodamine 123 to the green fluorescent rhodamine 123, measured by flow cytometry. Assay conditions, including bacterial and dihydrorhodamine 123 concentrations and incubation time, were determined. Repeatability and precision of the method were assessed by testing parallel samples from clinically healthy dairy cows. In vitro and in vivo inhibition of respiratory burst was investigated, and labelling with a granulocyte marker antibody was performed. Stimulation with live S. aureus induced green fluorescence in the neutrophil granulocytes in a whole blood preparation. The fluorescence intensity increased with increasing bacterial concentration and increasing incubation time. Agreement analysis showed that the method gave repeatable results, and the intra-assay variability of the method was relatively low. The method is considered a useful technique for measurement of neutrophil respiratory burst in whole bovine blood.
本文描述了一种快速简便的方法,用于测量全血中牛中性粒细胞的呼吸爆发。用活的金黄色葡萄球菌刺激呼吸爆发,并通过流式细胞术测量细胞内二氢罗丹明123转化为绿色荧光罗丹明123来定量活性氧的产生。确定了包括细菌和二氢罗丹明123浓度以及孵育时间在内的检测条件。通过检测临床健康奶牛的平行样本评估了该方法的重复性和精密度。研究了体外和体内对呼吸爆发的抑制作用,并进行了粒细胞标记抗体标记。用活的金黄色葡萄球菌刺激可在全血制备物中的中性粒细胞中诱导绿色荧光。荧光强度随着细菌浓度的增加和孵育时间的延长而增加。一致性分析表明该方法可得到可重复的结果,且该方法的批内变异性相对较低。该方法被认为是测量全血中牛中性粒细胞呼吸爆发的一种有用技术。