Bullock W W, Creamer H R, Gabler W L
Inflammation. 1982 Sep;6(3):305-18. doi: 10.1007/BF00916411.
We present here a rapid, sensitive, and convenient assay for activated human PMNs based on detecting the decreased optical density (OD) of aggregated cell suspensions. This quantitative assay uses an ELIZA machine to measure OD changes, with time, of activated cells (5 X 10(5) cells/well) in microtiter plates. The assay is sensitive, detecting aggregation induced by as little as 0.0001 microgram/ml of LPS, or lymphokines in Con-A-activated supernatant diluted 1/500. The assay permits analysis of 400 separate PMN suspensions on the same day starting with less than 80 ml of blood.
我们在此展示一种基于检测聚集细胞悬液光密度(OD)降低的快速、灵敏且便捷的活化人中性粒细胞检测方法。这种定量检测方法使用酶联免疫吸附测定(ELISA)仪来测量微孔板中活化细胞(5×10⁵个细胞/孔)随时间的OD变化。该检测方法灵敏,能检测到低至0.0001微克/毫升的脂多糖(LPS)或经1/500稀释的伴刀豆球蛋白A(Con - A)活化上清液中的淋巴因子所诱导的聚集。该检测方法允许在同一天从少于80毫升血液开始分析400个单独的中性粒细胞悬液。