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TREM-1 multimerization is essential for its activation on monocytes and neutrophils

机译:TREM-1多聚化对其在单核细胞和中性粒细胞上的激活至关重要

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摘要

– U937 and U937-TD cells were stimulated with TREM-1 agonists αTREM-1 and Fab (10 µg/ml) with or without GαM (10 µg/ml) when indicated. Kinetics of intracellular calcium release in U937 cells. Left panel: TREM-1 expression on U937 (gray) and U937-TD (black) cells. Right panel: kinetics of intracellular calcium release in U937-TD cells. , Kinetics of intracellular calcium release in U937-TD cells incubated with increasing concentrations of αTREM-1 (0.1–20 µg/ml) and with αTREM-1 (5 µg/ml) and increasing concentrations of GαM (2.5–10 µg/ml). Western blot analysis of lysates of U937 and U937-TD cells at indicated times. IL-8 concentrations in supernatants after a 24-h stimulation. Data information: data are representative of at least three independent experiments. MFI mean fluorescence intensity, ns nonsignificant. *  p p t-test
机译:–指示时,用TREM-1激动剂αTREM-1和Fab(10μg/ ml)加或不加GαM(10μg/ ml)刺激U937和U937-TD细胞。 U937细胞中细胞内钙释放的动力学。左图:TREM-1在U937(灰色)和U937-TD(黑色)细胞上的表达。右图:U937-TD细胞中细胞内钙释放的动力学。 ,随着浓度增加的αTREM-1(0.1–20μg / ml)和浓度增加的αTREM-1(5μµg / ml)和浓度增加的GαM(2.5–10μg / ml)孵育的U937-TD细胞内钙释放动力学)。在指定时间对U937和U937-TD细胞的裂解液进行蛋白质印迹分析。 24小时刺激后上清液中的IL-8浓度。数据信息:数据代表至少三个独立的实验。 MFI平均荧光强度,ns不显着。 * p t t检验

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