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肥大细胞通过FcγR诱导肿瘤坏死因子-α的产生。FcγRIIIγ亚基的作用。

Induction of tumor necrosis factor-alpha production by mast cells via Fc gamma R. Role of the Fc gamma RIII gamma subunit.

作者信息

Latour S, Bonnerot C, Fridman W H, Daëron M

机构信息

Laboratoire d'Immunologie Cellulaire et Clinique, INSERM U. 255, Institut Curie, Paris, France.

出版信息

J Immunol. 1992 Sep 15;149(6):2155-62.

PMID:1387672
Abstract

Murine mast cells produce cytokines in response to cross-linking of high affinity receptors for IgE (Fc epsilon RI). Murine mast cells also express the two types of low-affinity receptors for IgG, murine (m)Fc gamma RII, and mFc gamma RIII. We examined the ability of mFc gamma R to trigger a cytokine response such as TNF-alpha production by mast cells. We found that the mFc gamma RII- and mFc gamma RIII-positive mouse mastocytoma cells MMC-1 released TNF-alpha when challenged with F(ab')2 fragments of the rat anti-mFc gamma RII/III 2.4G2 mAb and mouse anti-rat IgG F(ab')2. The release of TNF-alpha was preceded by an increase in TNF-alpha transcripts. mFc gamma RII and mFc gamma RIII have 95% homologous extracellular domains but unrelated transmembrane and intracytoplasmic (IC) domains. mFc gamma RII are single chain receptors whereas mFc gamma RIII associate with a homodimeric gamma-chain that also associates with Fc epsilon RI and TCR. In order to analyze the ability of mFc gamma RII and III to trigger the synthesis of TNF-alpha, we studied RBL-2H3 cells transfected with corresponding cDNA. Rat basophilic leukemia (RBL) transfectants expressing mFc gamma RIII produced TNF-alpha in response to 2.4G2 F(ab')2, but not transfectants expressing mFc gamma RII. Non-transfected RBL cells and mFc gamma RII- or mFc gamma RIII-expressing transfectants, however, released TNF-alpha in response to a rat IgG2a mAb. The respective roles of the alpha and gamma subunits of mFc gamma RIII were examined by studying the production of TNF-alpha by RBL cells expressing deletant and chimeric mFc gamma R. The deletion of intracellular amino acids of the Fc gamma RIII alpha subunit did not prevent 2.4G2 F(ab')2 from triggering the synthesis of TNF-alpha. The substitution of the IC domain of mFc gamma RII for that of mFc gamma RIII gamma, but not that of Fc gamma RIII alpha, enabled 2.4G2 F(ab')2 to trigger the release of TNF-alpha by RBL transfectants. A cytokine response can therefore be induced in mouse and rat mast cells through Fc gamma R. This response is triggered upon cross-linking of mFc gamma RIII but not mFc gamma RII. It depends on the IC sequences of the gamma but not of the alpha subunit of mFc gamma RIII.

摘要

小鼠肥大细胞在高亲和力IgE受体(FcεRI)交联时会产生细胞因子。小鼠肥大细胞还表达两种类型的IgG低亲和力受体,即小鼠(m)FcγRII和mFcγRIII。我们研究了mFcγR触发肥大细胞产生细胞因子(如TNF-α)的能力。我们发现,mFcγRII和mFcγRIII阳性的小鼠肥大细胞瘤细胞系MMC-1在用大鼠抗mFcγRII/III 2.4G2单克隆抗体的F(ab')2片段和小鼠抗大鼠IgG F(ab')2刺激时会释放TNF-α。TNF-α的释放之前是TNF-α转录本的增加。mFcγRII和mFcγRIII的细胞外结构域有95%的同源性,但跨膜和胞质内(IC)结构域无关。mFcγRII是单链受体,而mFcγRIII与同二聚体γ链结合,γ链也与FcεRI和TCR结合。为了分析mFcγRII和III触发TNF-α合成的能力,我们研究了用相应cDNA转染的RBL-2H3细胞。表达mFcγRIII的大鼠嗜碱性白血病(RBL)转染细胞在受到2.4G2 F(ab')2刺激时会产生TNF-α,但表达mFcγRII的转染细胞则不会。然而,未转染的RBL细胞以及表达mFcγRII或mFcγRIII的转染细胞在受到大鼠IgG2a单克隆抗体刺激时会释放TNF-α。通过研究表达缺失和嵌合mFcγR的RBL细胞中TNF-α的产生,我们检测了mFcγRIII的α和γ亚基各自的作用。FcγRIIIα亚基细胞内氨基酸的缺失并不能阻止2.4G2 F(ab')2触发TNF-α的合成。用mFcγRII的IC结构域替换mFcγRIIIγ的IC结构域(而不是FcγRIIIα的IC结构域)能使2.4G2 F(ab')2触发RBL转染细胞释放TNF-α。因此,通过FcγR可以在小鼠和大鼠肥大细胞中诱导细胞因子反应。这种反应是在mFcγRIII交联时而不是mFcγRII交联时触发的。它取决于mFcγRIIIγ亚基而不是α亚基的IC序列。

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