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一种用于测定携带C1q受体细胞的玫瑰花结试验。

A rosette assay for the determination of C 1 q receptor-bearing cells.

作者信息

Gabay Y, Perlmann H, Perlmann P, Sobel A T

出版信息

Eur J Immunol. 1979 Oct;9(10):797-801. doi: 10.1002/eji.1830091010.

Abstract

A rosette assay for the identification of cells with receptors for C 1 q is described. Glutaraldehyde-treated bovine erythrocytes bound C 1 q specifically, and the reagent thus prepared provided a valid indicator for rosette formation mediated by C 1 q receptors. The presence of these receptors on the membrane of a subset of human peripheral lymphocytes (mainly non-G cells) and on B-derived lymphoblastoid cells was confirmed. Rosette formation was dependent on the number of C 1 q molecules bound per indicator cell and was specifically inhibited by soluble native C 1 q and pepsin-resistant C 1 q fragments. These data, together with the reduced binding activity of C 1 r-C 1 s-associated C 1 q, indicated that the C 1 q binding sites for lymphoid membranes are expressed on the collagen-like moiety, C 1 q rosette formation provided a simple new procedure for fractionation of human lymphocyte populations and separation from phagocytes that do not express receptors for C 1 q.

摘要

本文描述了一种用于鉴定具有C1q受体的细胞的玫瑰花结试验。经戊二醛处理的牛红细胞可特异性结合C1q,由此制备的试剂为C1q受体介导的玫瑰花结形成提供了有效的指示物。已证实人外周淋巴细胞亚群(主要是非G细胞)和B衍生的淋巴母细胞的膜上存在这些受体。玫瑰花结的形成取决于每个指示细胞结合的C1q分子数量,并受到可溶性天然C1q和胃蛋白酶抗性C1q片段的特异性抑制。这些数据,连同C1r-C1s相关C1q的结合活性降低,表明淋巴细胞膜的C1q结合位点在胶原样部分表达,C1q玫瑰花结形成提供了一种简单的新方法,用于分离人淋巴细胞群体并与不表达C1q受体的吞噬细胞分离。

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