Chuang F Y, Sassaroli M, Unkeless J C
Department of Biochemistry, Mount Sinai School of Medicine, New York 10029, USA.
J Immunol. 2000 Jan 1;164(1):350-60. doi: 10.4049/jimmunol.164.1.350.
Human neutrophils (PMNs) express two receptors for the Fc domain of IgG: the transmembrane FcgammaRIIA, whose cytosolic sequence contains an immunoreceptor tyrosine-based activation motif, and the GPI-anchored FcgammaRIIIB. Cross-linking of FcgammaRIIIB induces cell activation, but the mechanism is still uncertain. We have used mAbs to cross-link selectively each of the two receptors and to assess their signaling phenotypes and functional relation. Cross-linking of FcgammaRIIIB induces intracellular Ca2+ release and receptor capping. The Ca2+ response is blocked by wortmannin and by N,N-dimethylsphingosine, inhibitors of phosphatidylinositol 3-kinase and sphingosine kinase, respectively. Identical dose-response curves are obtained for the Ca2+ release stimulated by cross-linking FcgammaRIIA, implicating these two enzymes in a common signaling pathway. Wortmannin also inhibits capping of both receptors, but not receptor endocytosis. Fluorescence microscopy in double-labeled PMNs demonstrates that FcgammaRIIA colocalizes with cross-linked FcgammaRIIIB. The signaling phenotypes of the two receptors diverge only under frustrated phagocytosis conditions, where FcgammaRIIIB bound to substrate-immobilized Ab does not elicit cell spreading. We propose that FcgammaRIIIB signaling is conducted by molecules of FcgammaRIIA that are recruited to protein/lipid domains induced by clustered FcgammaRIIIB and, thus, are brought into juxtaposition for immunoreceptor tyrosine-based activation motif phosphorylation and activation of PMNs.
人类中性粒细胞(PMN)表达两种针对IgG Fc结构域的受体:跨膜的FcγRIIA,其胞质序列包含基于免疫受体酪氨酸的激活基序,以及糖基磷脂酰肌醇(GPI)锚定的FcγRIIIB。FcγRIIIB的交联可诱导细胞活化,但其机制仍不确定。我们使用单克隆抗体(mAb)分别选择性交联这两种受体,并评估它们的信号表型和功能关系。FcγRIIIB的交联可诱导细胞内Ca2+释放和受体成帽。Ca2+反应分别被渥曼青霉素和N,N-二甲基鞘氨醇阻断,它们分别是磷脂酰肌醇3激酶和鞘氨醇激酶的抑制剂。由FcγRIIA交联刺激的Ca2+释放获得相同的剂量反应曲线,表明这两种酶参与共同的信号通路。渥曼青霉素也抑制两种受体的成帽,但不抑制受体内吞作用。双标记PMN的荧光显微镜检查表明,FcγRIIA与交联的FcγRIIIB共定位。仅在吞噬受挫条件下,两种受体的信号表型才会出现差异,此时与底物固定抗体结合的FcγRIIIB不会引发细胞铺展。我们提出,FcγRIIIB信号传导是由FcγRIIA分子介导的,这些分子被募集到由聚集的FcγRIIIB诱导的蛋白质/脂质结构域中,从而并列排列以进行基于免疫受体酪氨酸的激活基序磷酸化和PMN的激活。