Suppr超能文献

小鼠浆膜肥大细胞、培养来源的肥大细胞和病毒转化的肥大细胞共有的肥大细胞质膜抗原的生化特性

Biochemical characterization of a mast cell plasma membrane antigen shared by mouse serosal, culture-derived, and virally transformed mast cells.

作者信息

Katz H R, Austen K F

出版信息

J Immunol. 1987 Feb 15;138(4):1196-200.

PMID:2433344
Abstract

The expression of the antigenic determinant identified by the B54.2 rat monoclonal antibody on four populations of mouse mast cells has been quantified, and the epitope-bearing surface antigen and its biosynthesis have been characterized. As assessed by indirect immunofluorescence staining and flow cytometric analysis, B54.2 antibody bound to serosal mast cells (S-MC), bone marrow culture-derived mast cells (BM-MC), fetal liver culture-derived mast cells (FTL-MC), and Abelson murine leukemia virus-transformed FTL-MC (ABFTL-MC). However, the intensity of cell surface fluorescence exhibited by ABFTL-MC was approximately eightfold less per cell compared with nontransformed, culture-derived mast cells. Immunoprecipitation of B54.2 antibody-binding molecules from each population of mast cells labeled intrinsically with [35S]methionine and analysis by SDS-PAGE demonstrated that the B54.2 epitope was expressed in each case on two noncovalently associated proteins of 110,000 Mr and approximately 130,000 Mr, but that the percentage of radiolabel in the latter species was approximately threefold less in ABFTL-MC than in BM-MC. As assessed by pulse-chase analysis with [35S]methionine, the 110,000 Mr protein was a precursor of the 130,000 Mr molecule ("B54.2 antigen") synthesized by BM-MC. Labeling of BM-MC with [35S]methionine in the presence of tunicamycin followed by immunoprecipitation and SDS-PAGE of B54.2 antibody-binding material revealed a single species of 93,000 Mr, indicating that the native molecules contained N-linked carbohydrate. Endoglycosidase H treatment of the glycoproteins precipitated by B54.2 antibody from BM-MC reduced the Mr of the 110,000-Mr molecule to 93,000 Mr without an appreciable change in the 130,000-Mr species. These data indicate that the 110,000-Mr precursor form is a "high mannose" type glycoprotein and the 130,000-Mr membrane surface B54.2 antigen is a "complex" type glycoprotein, and that the epitope recognized by the B54.2 antibody on the surface of the mouse mast cell populations is located on the 93,000-Mr peptide core.

摘要

已对由B54.2大鼠单克隆抗体识别的抗原决定簇在四群小鼠肥大细胞上的表达进行了定量,并对携带该表位的表面抗原及其生物合成进行了表征。通过间接免疫荧光染色和流式细胞术分析评估,B54.2抗体与浆膜肥大细胞(S-MC)、骨髓培养来源的肥大细胞(BM-MC)、胎肝培养来源的肥大细胞(FTL-MC)以及阿伯尔逊鼠白血病病毒转化的FTL-MC(ABFTL-MC)结合。然而,与未转化的培养来源肥大细胞相比,ABFTL-MC每个细胞呈现的细胞表面荧光强度约低八倍。从用[35S]甲硫氨酸进行内在标记的各群肥大细胞中免疫沉淀B54.2抗体结合分子,并通过SDS-PAGE分析表明,在每种情况下,B54.2表位均在110,000 Mr和大约130,000 Mr的两种非共价结合蛋白上表达,但在ABFTL-MC中,后一种蛋白中的放射性标记百分比比在BM-MC中约低三倍。通过用[35S]甲硫氨酸进行脉冲追踪分析评估,110,000 Mr蛋白是BM-MC合成的130,000 Mr分子(“B54.2抗原”)的前体。在衣霉素存在下用[35S]甲硫氨酸标记BM-MC,随后对B54.2抗体结合物质进行免疫沉淀和SDS-PAGE,结果显示有单一的93,000 Mr条带,表明天然分子含有N-连接的碳水化合物。用内切糖苷酶H处理由B54.2抗体从BM-MC沉淀的糖蛋白,使110,000-Mr分子的Mr降至93,000 Mr,而130,000-Mr条带没有明显变化。这些数据表明,110,000-Mr前体形式是一种“高甘露糖”型糖蛋白,130,000-Mr膜表面B54.2抗原是一种“复杂”型糖蛋白,并且小鼠肥大细胞群体表面上被B54.2抗体识别的表位位于93,000-Mr肽核心上。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验