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肠道上皮内T细胞上HML-1抗原以及毛细胞白血病中B-ly7抗原的特性

Identity of HML-1 antigen on intestinal intraepithelial T cells and of B-ly7 antigen on hairy cell leukaemia.

作者信息

Moldenhauer G, Mielke B, Dörken B, Schwartz-Albiez R, Möller P

机构信息

Institute of Immunology and Genetics, German Cancer Research Centre, University of Heidelburg.

出版信息

Scand J Immunol. 1990 Aug;32(2):77-82. doi: 10.1111/j.1365-3083.1990.tb02896.x.

Abstract

Immunoprecipitation of radioiodinated hairy cell leukaemia (HCL) cell lysates with monoclonal antibody (MoAb) HML-1, originally reported to recognize intraepithelial T cells, and with MoAb B-ly7, originally reported to react with HCL, led to identical biochemical characteristics. In SDS-PAGE under reducing conditions, a major band of 143 kDa, a broad band ranging from 112 to 122 kDa, and two additional faint bands of 175 and 100 kDa could be determined. Deglycosylation of N-linked sugar moieties by treatment of immunoprecipitates with endoglycosidases indicated that the two main protein cores of the antigen are predominantly if not exclusively glycosylated by complex and hybrid types of oligosaccharide chains. Competitive binding inhibition demonstrated that both MoAb are directed against different epitopes. Immunohistochemically, the staining patterns obtained with both MoAb in normal tissues, in T- and B-cell lymphomas, and in HCL were identical except for a single case of HCL which was HML-1-/B-ly-7+. We conclude that MoAb HML-1 and B-ly7 recognize the same antigen.

摘要

用单克隆抗体(MoAb)HML - 1(最初报道可识别上皮内T细胞)和MoAb B - ly7(最初报道可与毛细胞白血病(HCL)反应)对放射性碘化的HCL细胞裂解物进行免疫沉淀,得到了相同的生化特征。在还原条件下的SDS - PAGE中,可确定一条143 kDa的主要条带、一条112至122 kDa的宽带以及另外两条175 kDa和100 kDa的微弱条带。用内切糖苷酶处理免疫沉淀物对N - 连接糖基进行去糖基化表明,抗原的两个主要蛋白核心主要(如果不是唯一的话)被复杂型和杂合型寡糖链糖基化。竞争性结合抑制表明两种单克隆抗体针对不同的表位。免疫组织化学分析显示,除了一例HCL为HML - 1阴性/B - ly - 7阳性外,两种单克隆抗体在正常组织、T细胞和B细胞淋巴瘤以及HCL中获得的染色模式相同。我们得出结论,单克隆抗体HML - 1和B - ly7识别相同的抗原。

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