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鉴定C3β链为人血清嗜酸性粒细胞细胞毒性抑制剂。

Identification of C3 beta chain as the human serum eosinophil cytotoxicity inhibitor.

作者信息

Minkoff M S, Wong W W, Silberstein D S

机构信息

Department of Rheumatology and Immunology, Brigham and Women's Hospital, Boston, Massachusetts.

出版信息

J Exp Med. 1991 Nov 1;174(5):1267-70. doi: 10.1084/jem.174.5.1267.

Abstract

An eosinophil cytotoxicity inhibitor (ECI) was purified from serum of a human subject with severe allergic dermatitis. Molecular weight of the isolated polypeptide (75,000) and its NH2-terminal amino acid sequence identified it as the beta chain of the C3 complement component (apparently free, but perhaps attached to very small fragments of the alpha chain). Free beta chain, prepared from normal plasma by reduction of C3, inhibited both eosinophil cytotoxicity and neutrophil adherence functions, with half-maximal activity at approximately 250 ng/ml. Apparently free C3 beta chain was detected in certain human biological fluids associated with inflammation; the presence of C3 beta chain correlated with ECI activity. This evidence demonstrates a potential role for free C3 beta chain as a suppressor of eosinophil and neutrophil functions in inflammation.

摘要

从一名患有严重过敏性皮炎的人类受试者血清中纯化出一种嗜酸性粒细胞细胞毒性抑制剂(ECI)。分离出的多肽分子量为75,000,其氨基末端氨基酸序列表明它是C3补体成分的β链(显然是游离的,但可能与α链的非常小的片段相连)。通过还原C3从正常血浆中制备的游离β链,抑制嗜酸性粒细胞细胞毒性和中性粒细胞黏附功能,在约250 ng/ml时具有半数最大活性。在某些与炎症相关的人类生物体液中检测到明显游离的C3β链;C3β链的存在与ECI活性相关。这一证据表明游离C3β链作为炎症中嗜酸性粒细胞和中性粒细胞功能抑制剂的潜在作用。

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本文引用的文献

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Membrane complement receptors specific for bound fragments of C3.
Adv Immunol. 1985;37:217-67. doi: 10.1016/s0065-2776(08)60341-7.

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