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Respective contribution of intracellular calcium release and extracellular calcium influx for interleukin-2 synthesis in activated T-cell hybrids.

机译:细胞内钙释放和细胞外钙内流对于活化T细胞杂种中白细胞介素2合成的贡献。

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摘要

Triggering of the T-cell receptor (TcR)alpha beta/CD3 receptor complex with anti-allotypic antibodies or concanavalin A (Con A) induced a rapid release of intracellular calcium in a murine T-cell hybridoma model system. Internal calcium release preceded the influx of extracellular calcium, as judged by comparative analysis of time-dependent changes in Quin 2 fluorescence following T-cell activation in the presence and absence of extracellular calcium. The magnitude of intracellular calcium release and extracellular calcium influx depended on the degree of receptor-occupancy and cross-linking. Correlations between the concentration of stimulating ligand, cytosolic calcium increase and IL-2 synthesis indicated a positive but non-linear relationship. Our data suggest that TcR cross-linking may provide a third T-cell activation signal which, in conjunction with protein kinase C activation and cytosolic calcium elevation, together form a signal triad responsible for interleukin-2 (IL-2) synthesis.
机译:用抗allottypic抗体或伴刀豆球蛋白A(Con A)触发T细胞受体(TcR)αbeta / CD3受体复合物可在鼠T细胞杂交瘤模型系统中快速释放细胞内钙。通过对存在和不存在细胞外钙的情况下T细胞活化后Quin 2荧光的时间依赖性变化的比较分析判断,内部钙的释放先于细胞外钙的流入。细胞内钙释放和细胞外钙内流的程度取决于受体占有和交联的程度。刺激性配体的浓度,胞质钙的增加与IL-2合成之间的相关性显示出正但非线性的关系。我们的数据表明,TcR交联可提供第三种T细胞激活信号,该信号与蛋白激酶C激活和胞质钙升高一起形成负责白介素2(IL-2)合成的信号三联体。

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