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人红细胞的C8结合蛋白:与补体攻击阶段各成分的相互作用。

The C8-binding protein of human erythrocytes: interaction with the components of the complement-attack phase.

作者信息

Schönermark S, Filsinger S, Berger B, Hänsch G M

机构信息

Institut für Immunologie, Universität Heidelberg, FRG.

出版信息

Immunology. 1988 Apr;63(4):585-90.

PMID:3366469
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1454802/
Abstract

C8-binding protein is an intrinsic membrane protein of the human erythrocyte. It inhibits the complement (C5b-9)-mediated lysis in a species-restricting manner. In the present study we incorporated C8bp, isolated from human erythrocytes, into sheep erythrocytes (SRBC). SRBC, normally sensitive to lysis by human C5b-9, became insensitive to lysis. Furthermore, we found that C8bp is incorporated into the membrane-attack complex C5b-9, most probably by interacting with C8, since C8bp has an affinity for C8, particularly for the C8 alpha-gamma-subunit. Antibodies to C8bp react with the C8 alpha-subunits and with C9, pointing to the possibility of a partial homology between these proteins.

摘要

C8结合蛋白是人类红细胞的一种内在膜蛋白。它以物种限制的方式抑制补体(C5b-9)介导的细胞溶解。在本研究中,我们将从人类红细胞中分离出的C8结合蛋白(C8bp)整合到绵羊红细胞(SRBC)中。通常对人类C5b-9介导的细胞溶解敏感的SRBC变得对细胞溶解不敏感。此外,我们发现C8bp整合到膜攻击复合物C5b-9中,很可能是通过与C8相互作用,因为C8bp对C8有亲和力,特别是对C8α-γ亚基。针对C8bp的抗体与C8α亚基和C9发生反应,表明这些蛋白之间可能存在部分同源性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/191d/1454802/e5a81a210bbd/immunology00161-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/191d/1454802/6d3acd57f0b9/immunology00161-0026-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/191d/1454802/b03692640fb5/immunology00161-0026-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/191d/1454802/e5a81a210bbd/immunology00161-0027-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/191d/1454802/6d3acd57f0b9/immunology00161-0026-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/191d/1454802/b03692640fb5/immunology00161-0026-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/191d/1454802/e5a81a210bbd/immunology00161-0027-a.jpg

相似文献

1
The C8-binding protein of human erythrocytes: interaction with the components of the complement-attack phase.人红细胞的C8结合蛋白:与补体攻击阶段各成分的相互作用。
Immunology. 1988 Apr;63(4):585-90.
2
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3
Paroxysmal nocturnal hemoglobinuria. Enhanced stimulation of platelets by the terminal complement components is related to the lack of C8bp in the membrane.阵发性夜间血红蛋白尿。终末补体成分对血小板的刺激增强与膜中缺乏C8结合蛋白有关。
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5
Regulation of the membrane attack complex of complement. Evidence that C8 gamma is not the target of homologous restriction factors.补体膜攻击复合物的调节。有证据表明C8γ不是同源限制因子的作用靶点。
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6
Homologous species restriction in lysis of human erythrocytes: a membrane-derived protein with C8-binding capacity functions as an inhibitor.人红细胞裂解中的同源物种限制:一种具有C8结合能力的膜衍生蛋白发挥抑制剂作用。
J Immunol. 1986 Mar 1;136(5):1772-6.
7
Enhanced expression of the complement-regulatory factor C8 binding protein (C8bp) on U937 cells after stimulation with IL-1 beta, endotoxin, IFN-gamma, or phorbol ester.在用白细胞介素-1β、内毒素、γ干扰素或佛波酯刺激后,U937细胞上补体调节因子C8结合蛋白(C8bp)的表达增强。
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Incorporation of human complement C8 into the membrane attack complex is mediated by a binding site located within the C8beta MACPF domain.人补体C8整合到膜攻击复合物中是由位于C8βMACPF结构域内的一个结合位点介导的。
Mol Immunol. 2007 Feb;44(5):960-5. doi: 10.1016/j.molimm.2006.03.012. Epub 2006 Apr 19.
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A synthetic peptide from complement protein C9 binds to CD59 and enhances lysis of human erythrocytes by C5b-9.一种来自补体蛋白C9的合成肽与CD59结合,并增强C5b-9对人红细胞的裂解作用。
J Immunol. 1994 Feb 15;152(4):1927-34.

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本文引用的文献

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The eighth component of human complement. Purification and physicochemical characterization of its unusual subunit structure.人类补体的第八个成分。其异常亚基结构的纯化及理化特性
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Binding of the eighth component of human complement to the soluble cytolytic complex is mediated by its beta subunit.人补体第八成分与可溶性溶细胞复合物的结合是由其β亚基介导的。
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Inhibition of immune haemolysis by a serum factor found in C3-deficient subjects.在C3缺陷患者血清中发现的一种血清因子对免疫性溶血的抑制作用。
Immunology. 1989 Feb;66(2):264-9.
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Complement membrane attack on nucleated cells: resistance, recovery and non-lethal effects.补体对有核细胞的膜攻击:抗性、恢复及非致死效应。
Biochem J. 1989 Nov 15;264(1):1-14. doi: 10.1042/bj2640001.
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CD59, an LY-6-like protein expressed in human lymphoid cells, regulates the action of the complement membrane attack complex on homologous cells.CD59是一种在人类淋巴细胞中表达的类LY-6蛋白,可调节补体膜攻击复合物对同源细胞的作用。
J Exp Med. 1989 Sep 1;170(3):637-54. doi: 10.1084/jem.170.3.637.
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Isolation and characterization of a membrane-attack-complex-inhibiting protein present in human serum and other biological fluids.人血清及其他生物体液中存在的膜攻击复合物抑制蛋白的分离与特性鉴定。
Biochem J. 1990 Jan 15;265(2):471-7. doi: 10.1042/bj2650471.
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C8 binding protein bears I antigenic determinants.C8结合蛋白带有I抗原决定簇。
Ann Hematol. 1991 Feb-Mar;62(2-3):64-7. doi: 10.1007/BF01714902.
补体第九成分的环状聚合。管状复合物的环化赋予其对去污剂解离和蛋白水解降解的抗性。
J Biol Chem. 1982 Dec 25;257(24):15204-12.
4
Homologous species restriction in lysis of erythrocytes by terminal complement proteins.终末补体蛋白对红细胞溶解的同源物种限制
Proc Natl Acad Sci U S A. 1981 Aug;78(8):5118-21. doi: 10.1073/pnas.78.8.5118.
5
Evidence of direct insertion of terminal complement proteins into cell membrane bilayers during cytolysis. Labeling by a photosensitive membrane probe reveals a major role for the eighth and ninth components.细胞溶解过程中末端补体蛋白直接插入细胞膜双层结构的证据。用光敏膜探针标记显示第八和第九成分起主要作用。
J Biol Chem. 1983 Apr 10;258(7):4318-24.
6
Affected erythrocytes of patients with paroxysmal nocturnal hemoglobinuria are deficient in the complement regulatory protein, decay accelerating factor.阵发性夜间血红蛋白尿患者的受累红细胞缺乏补体调节蛋白衰变加速因子。
Proc Natl Acad Sci U S A. 1983 Aug;80(16):5066-70. doi: 10.1073/pnas.80.16.5066.
7
Species-restricted target cell lysis by human complement: complement-lysed erythrocytes from heterologous and homologous species differ in their ratio of bound to inserted C9.人类补体介导的物种特异性靶细胞裂解:来自异源和同源物种的补体裂解红细胞在结合C9与插入C9的比例上存在差异。
J Immunol. 1984 Oct;133(4):2133-7.
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Membrane attack by complement.补体介导的膜攻击。
Mol Immunol. 1984 Jul;21(7):589-603. doi: 10.1016/0161-5890(84)90044-0.
9
Inhibition of complement activation on the surface of cells after incorporation of decay-accelerating factor (DAF) into their membranes.衰变加速因子(DAF)整合到细胞膜后对细胞表面补体激活的抑制作用。
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Paroxysmal nocturnal hemoglobinuria: deficiency in factor H-like functions of the abnormal erythrocytes.阵发性夜间血红蛋白尿:异常红细胞中类似补体因子H功能的缺陷。
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