Daëron M, Bonnerot C, Latour S, Fridman W H
Laboratoire d'Immunologie Cellulaire et Clinique, INSERM U255, Institut Curie, Paris, France.
J Immunol. 1992 Aug 15;149(4):1365-73.
Murine Fc gamma RII and Fc gamma RIII have highly homologous extracellular domains, but unrelated transmembrane and intracytoplasmic (IC) domains. Murine Fc gamma RIIb1 and b2 are two isoforms of single-chain receptors which differ only by 47 aa in their IC domain. Murine Fc gamma RIII are composed of an IgG-binding alpha-chain, the intracellular portion of which is unrelated to that of Fc gamma RII, and of a homodimeric gamma-chain which also associates with Fc epsilon RI. Murine mast cells express Fc gamma RII, Fc gamma RIII, and Fc epsilon RI. They can be induced to degranulate by murine IgG immune complexes or by F(ab')2 fragments of the rat anti-murine Fc gamma RII/III mAb 2.4G2, complexed to mouse anti-rat (MAR) F(ab')2. In order to determine which murine Fc gamma R can activate mast cells, cDNA encoding murine Fc gamma RIIb1, Fc gamma RIIb2 or Fc gamma RIII alpha were stably transfected into RBL-2H3 cells. Murine Fc gamma RIII but not Fc gamma RIIb1 or Fc gamma RIIb2 induced serotonin release when aggregated by (2.4G2-MAR) F(ab')2 complexes. The respective roles of the IC domains of murine Fc gamma RIII subunits in signal transduction were investigated by stably transfecting cDNA encoding IC-deleted or chimeric murine Fc gamma R into RBL-2H3 cells. The substitution of the IC domain of murine Fc gamma RII for that of murine Fc gamma RIII gamma, but not that of murine Fc gamma RIII alpha, conferred the ability to trigger serotonin release. The deletion of IC sequences of the alpha subunit did not alter the ability of murine Fc gamma RIII to trigger serotonin release. It follows that 1) murine Fc gamma RIII, but not Fc gamma RII, can induce RBL cells to release serotonin, 2) the aggregation of the IC domain of the murine Fc gamma RIII gamma subunit is sufficient, but 3) the IC domain of the murine Fc gamma RIII alpha subunit is neither sufficient nor necessary for triggering serotonin release.
小鼠FcγRII和FcγRIII具有高度同源的细胞外结构域,但跨膜结构域和胞质内(IC)结构域无关。小鼠FcγRIIb1和b2是单链受体的两种异构体,它们的IC结构域仅相差47个氨基酸。小鼠FcγRIII由一个结合IgG的α链组成,其细胞内部分与FcγRII的细胞内部分无关,还由一个同二聚体γ链组成,该γ链也与FcεRI结合。小鼠肥大细胞表达FcγRII、FcγRIII和FcεRI。它们可被小鼠IgG免疫复合物或与小鼠抗大鼠(MAR)F(ab')2复合的大鼠抗小鼠FcγRII/III单克隆抗体2.4G2的F(ab')片段诱导脱颗粒。为了确定哪种小鼠FcγR能激活肥大细胞,将编码小鼠FcγRIIb1、FcγRIIb2或FcγRIIIα的cDNA稳定转染到RBL-2H3细胞中。当被(2.4G2-MAR)F(ab')2复合物聚集时,小鼠FcγRIII而非FcγRIIb1或FcγRIIb2诱导5-羟色胺释放。通过将编码IC缺失或嵌合小鼠FcγR的cDNA稳定转染到RBL-2H3细胞中,研究了小鼠FcγRIII亚基的IC结构域在信号转导中的各自作用。用小鼠FcγRIIIγ的IC结构域替换小鼠FcγRII的IC结构域可赋予触发5-羟色胺释放的能力,但用小鼠FcγRIIIα的IC结构域替换则不能。α亚基IC序列的缺失并未改变小鼠FcγRIII触发5-羟色胺释放的能力。由此得出:1)小鼠FcγRIII而非FcγRII可诱导RBL细胞释放5-羟色胺;2)小鼠FcγRIIIγ亚基IC结构域的聚集就足够了;3)小鼠FcγRIIIα亚基的IC结构域对于触发5-羟色胺释放既不充分也不必要。