Suppr超能文献

F1 杂交小鼠中 H-2 抗原表达的变异:使用单克隆抗体进行分析

Variation in H-2 antigen expression in F1 hybrid mice: analysis using monoclonal antibodies.

作者信息

O'Neill H C, Blanden R V

出版信息

Aust J Exp Biol Med Sci. 1979 Dec;57(6):627-35. doi: 10.1038/icb.1979.66.

Abstract

Cells of (CBA/H X BALB/c)F1 hybrid mice express CBA/H-derived H-2k antigens more weakly than do CBA/H cells, but H-2d antigens are similarly expressed by F1 and BALB/c cells. This was evident when F1 hybrid macrophages were compared with CBA/H and BALB/c macrophages as targets for both alloreactive and H-2 restricted anti-viral TC cells. Quantitative absorption of anti-H-2Kk serum by spleen cells of F1 or CBA/H mice also suggested about 3-fold less H-2Kk antigen on F1 cells. With the use of two anti-H-2Kk monoclonal antibodies, 30R3 and 27R9, the reduced expression of H-2Kk in this F1 hybrid was further analysed in a two-stage radio-immunoassay employing the uptake of 125I-protein A to measure antibody binding. By a thermodynamic approach, estimates were made of the dissociation constant for antibody binding, and of the relative numbers of H-2 molecules expressed by both F1 hybrid and CBA/H spleen cells. The results indicate that there is a two-fold reduction in the number of H-2Kk molecules expressed on the surface of F1 cells. Similar dissociation constants for F1 and CBA/H cells indicated no detectable qualitative difference in their H-2Kk antigens with respect to sites recognized by 30R3 and 27R9.

摘要

(CBA/H×BALB/c)F1杂交小鼠的细胞表达源自CBA/H的H-2k抗原的程度比CBA/H细胞弱,但F1细胞和BALB/c细胞对H-2d抗原的表达相似。当将F1杂交巨噬细胞与CBA/H和BALB/c巨噬细胞作为同种异体反应性和H-2限制性抗病毒TC细胞的靶细胞进行比较时,这一点很明显。用F1或CBA/H小鼠的脾细胞对抗H-2Kk血清进行定量吸收,也表明F1细胞上的H-2Kk抗原减少了约3倍。使用两种抗H-2Kk单克隆抗体30R3和27R9,在采用125I-蛋白A摄取来测量抗体结合的两阶段放射免疫分析中,进一步分析了该F1杂交体中H-2Kk表达的降低情况。通过热力学方法,估算了抗体结合的解离常数以及F1杂交体和CBA/H脾细胞表达的H-2分子的相对数量。结果表明,F1细胞表面表达的H-2Kk分子数量减少了两倍。F1细胞和CBA/H细胞相似的解离常数表明,就30R3和27R9识别的位点而言,它们的H-2Kk抗原在质量上没有可检测到的差异。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验