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补体激活调节分子HRF20在外周血单个核细胞上的表达。

Expression of HRF20, a regulatory molecule of complement activation, on peripheral blood mononuclear cells.

作者信息

Hideshima T, Okada N, Okada H

机构信息

Department of Microbiology, Fukuoka University School of Medicine, Japan.

出版信息

Immunology. 1990 Mar;69(3):396-401.

Abstract

HRF20 is a homologous restriction factor of 20,000 MW that prevents cells from membrane attack by homologous complement. HRF20 has been identified by a monoclonal antibody (mAb), 1F5, and is one of the phosphatidylinositol(PI)-anchored cell-surface glycoproteins. We analysed the distribution of HRF20 expressed on subsets of peripheral blood lymphocytes using 1F5. HRF20 is expressed in relatively large amounts on T cells. In contrast, adherent cells possess smaller amounts of HRF20 while having large quantities of decay-accelerating factor (DAF). Although DAF was shown to be deficient or present at rather low levels on NK cells, HRF20 was detected in 95% of large granular lymphocytes (LGL), as described by FACS analysis. We also determined the effect of 1F5 on both mononuclear leucocytes and T cells in terms of their growth response. The results show that 1F5 induces T-cell proliferation when cells are stimulated with interleukin-2 (IL-2). In addition, induction of proliferation is facilitated by cross-linking 1F5 with a second antibody. These results suggest that HRF20 expressed on T cells not only protects them from cytotoxic attack by homologous complement, but also may initiate intracellular signals leading to cell activation when they happen to be cross-linked.

摘要

HRF20是一种分子量为20000的同源限制因子,可防止细胞受到同源补体的膜攻击。HRF20已通过单克隆抗体(mAb)1F5鉴定,是磷脂酰肌醇(PI)锚定的细胞表面糖蛋白之一。我们使用1F5分析了外周血淋巴细胞亚群上表达的HRF20的分布。HRF20在T细胞上大量表达。相比之下,贴壁细胞的HRF20含量较少,而衰变加速因子(DAF)含量较高。尽管已证明NK细胞上的DAF缺乏或含量相当低,但如流式细胞术分析所述,在95%的大颗粒淋巴细胞(LGL)中检测到了HRF20。我们还根据生长反应确定了1F5对单核白细胞和T细胞的影响。结果表明,当细胞用白细胞介素-2(IL-2)刺激时,1F5可诱导T细胞增殖。此外,通过将1F5与第二抗体交联可促进增殖的诱导。这些结果表明,T细胞上表达的HRF20不仅能保护它们免受同源补体的细胞毒性攻击,而且当它们偶然交联时,还可能启动导致细胞活化的细胞内信号。

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