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在循环的人类正常白细胞和白血病白细胞以及与猴红细胞共培养的细胞上检测膜相关补体成分(C3和C4)。

The detection of membrane-associated complement components (C 3 and C 4) on circulating human normal and leukemic leukocytes and on cultured cells with monkey erythrocytes.

作者信息

Burns G F, Cawley J C

出版信息

Eur J Immunol. 1979 Oct;9(10):791-6. doi: 10.1002/eji.1830091009.

Abstract

Monkey erythrocyte (Mk) rosette formation is described as an exquisitely sensitive method for the detection of complement (C) components on the membrane of human leukocytes. Blocking of the immune adherence receptor on Mk blocked subsequent rosette formation as did pretreatment of leukocytes with antiserum to the C components C 3 and C 4. In vitro C deposition by immune complex formation with normal human lymphocytes enhanced Mk rosette formation, and this could be inhibited with antiserum to C 3. The use of Mk rosette formation revealed that cells from a wide variety of human lymphoid and myeloid leukemias carry membrane-bound C. It was also shown that several lymphoblastoid cell lines, including a T cell line, probably synthesize both C 3 and C 4. Mk rosette formation is not dependent on metabolic activity of the rosetting leukocyte, and it is suggested that this technique will be of value in detecting C deposition in a variety of situations.

摘要

猴红细胞(Mk)花环形成被描述为一种检测人白细胞膜上补体(C)成分的极其灵敏的方法。Mk上免疫黏附受体的阻断以及用针对补体成分C3和C4的抗血清对白细胞进行预处理,均会阻断随后的花环形成。与正常人淋巴细胞通过免疫复合物形成在体外沉积补体,增强了Mk花环形成,而这可用针对C3的抗血清加以抑制。利用Mk花环形成发现,多种人类淋巴样和髓样白血病细胞带有膜结合补体。还表明,包括一个T细胞系在内的几种淋巴母细胞系可能合成C3和C4。Mk花环形成不依赖于形成花环的白细胞的代谢活性,并且提示该技术在检测多种情况下的补体沉积中将具有价值。

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