Peck R
J Immunol Methods. 1985 Sep 3;82(1):131-40. doi: 10.1016/0022-1759(85)90232-7.
Human peripheral blood monocytes purified by counterflow centrifugal elutriation (CCE) showed an enhanced capacity to kill Listeria Monocytogenes and Staphylococcus aureus after activation with interferon-gamma (IFN gamma). Bactericidal activity was evaluated by a rapid colorimetric microassay based on the reduction of a tetrazolium dye, MTT. The amount of dye reduced was directly proportional to the number of viable bacteria present in each microwell. Comparison with a bacterial titration plate containing serial dilutions from stock of a known titer allowed calculation of bacterial numbers before and after exposure to macrophages. Results were read in a multiscan plate reader and compared closely with those obtained by serial dilution on agar plates (i.e., colony counts). The entire assay, i.e., culturing the monocytes, treatment with IFN gamma, addition of the bacteria, and quantitation of surviving viable bacteria, was performed in a single microtiter plate.
通过逆流离心淘析法(CCE)纯化的人外周血单核细胞在用γ干扰素(IFNγ)激活后,对单核细胞增生李斯特菌和金黄色葡萄球菌的杀伤能力增强。杀菌活性通过基于四唑盐染料MTT还原的快速比色微量测定法进行评估。还原的染料量与每个微孔中存活细菌的数量成正比。与含有已知滴度原液系列稀释液的细菌滴定板进行比较,可以计算出暴露于巨噬细胞前后的细菌数量。结果在多功能酶标仪中读取,并与在琼脂平板上通过系列稀释获得的结果(即菌落计数)进行密切比较。整个测定过程,即培养单核细胞、用IFNγ处理、添加细菌以及对存活活菌进行定量,均在单个微量滴定板中进行。