Davis W, Sage S O, Allen J M
Physiological Laboratory, University of Cambridge, UK.
Cell Calcium. 1994 Jul;16(1):29-36. doi: 10.1016/s0143-4160(05)80005-3.
We have used the calcium indicator, Fura-2, to investigate cytosolic calcium responses to cross-linking of monomeric IgG-occupied surface Fc gamma receptors (Fc gamma R), using populations of the human monocyte-like cell line, U937. The magnitude and duration of the calcium response observed, and the relative contribution to the response of internal stores and external calcium, are found to depend on the state of differentiation of these cells. Initial release of calcium from stores following Fc gamma R cross-linking is enhanced by prior treatment of U937 cells with both interferon-gamma, and, to a lesser extent, with dibutyryl cAMP. A large and prolonged entry of external calcium is observed in dibutyryl cAMP treated cells; this may be due to direct regulation of calcium channels by the low affinity receptor, Fc gamma RII (whose expression is up-regulated in these cells), since the smaller and more transient entry observed in interferon-gamma treated cells, (where the high affinity receptor, Fc gamma RI, is up-regulated) argues against a common pathway of store-mediated calcium entry.
我们使用钙指示剂Fura-2,以人单核细胞样细胞系U937群体为研究对象,来探究细胞溶质钙对占据表面Fcγ受体(FcγR)的单体IgG交联的反应。所观察到的钙反应的幅度和持续时间,以及细胞内储存钙和细胞外钙对反应的相对贡献,都取决于这些细胞的分化状态。在用γ干扰素,以及在较小程度上用二丁酰环磷腺苷(dibutyryl cAMP)预先处理U937细胞后,FcγR交联后从储存钙中最初释放的钙会增加。在二丁酰环磷腺苷处理的细胞中观察到大量且持续时间长的细胞外钙内流;这可能是由于低亲和力受体FcγRII(其表达在这些细胞中上调)对钙通道的直接调节,因为在γ干扰素处理的细胞中观察到较小且更短暂的内流(其中高亲和力受体FcγRI上调),这与储存介导的钙内流的共同途径相悖。