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单克隆抗体对人体组织和细胞系中HLA - G的反应模式:一项比较研究。

Reaction patterns of monoclonal antibodies to HLA-G in human tissues and on cell lines: a comparative study.

作者信息

Blaschitz A, Hutter H, Leitner V, Pilz S, Wintersteiger R, Dohr G, Sedlmayr P

机构信息

Institut für Histologie und Embryologie, Graz, Austria.

出版信息

Hum Immunol. 2000 Nov;61(11):1074-85. doi: 10.1016/s0198-8859(00)00207-x.

Abstract

We compared the immunohistochemical reaction patterns of HLA-G-specific antibodies 87G, 4H84, G233, 16G1, and BFL.1 on human placentas under three different preparative conditions and on cryosections of other human tissues. Human and murine cell lines, either naturally expressing or transfected with HLA-G, were analyzed for their reaction patterns by immunocytochemistry and flow cytometry. Antibodies HCA2, TP25.99, W6/32 to classical HLA class I, anti-beta(2)-m and various non-HLA-G expressing cell lines were used as controls. The binding ability of the antibodies depends on the histotechnical procedure used. 4H84 and HCA2 bind to HLA-G despite aldehyde fixation and also paraffin embedding. 87G does not bind HLA-G in studies involving fixation with aldehydes. G233 labels HLA-G in aldehyde fixed but not paraffin embedded tissues. By immunocytochemistry HLA-G2 is merely detected with antibodies 4H84 and HCA2. MAb 16G1 binds to HLA-Gsol transfected cell lines only. The HLA-G specificity of mAb BFL.1 was considered as doubtful because it failed to react with most of the HLA-G transfected cell lines. Binding of 87G to the surface of monocytes or U-937 cells stimulated with IFN-gamma and GM-CSF is an Fc-receptor mediated phenomenon.

摘要

我们比较了HLA-G特异性抗体87G、4H84、G233、16G1和BFL.1在三种不同制备条件下对人胎盘以及其他人体组织冰冻切片的免疫组化反应模式。通过免疫细胞化学和流式细胞术分析了天然表达或转染了HLA-G的人和鼠细胞系的反应模式。使用抗经典HLA I类的抗体HCA2、TP25.99、W6/32、抗β2微球蛋白以及各种不表达HLA-G的细胞系作为对照。抗体的结合能力取决于所采用的组织技术程序。尽管经过醛固定和石蜡包埋,4H84和HCA2仍能与HLA-G结合。在涉及醛固定的研究中,87G不与HLA-G结合。G233在醛固定但未石蜡包埋的组织中标记HLA-G。通过免疫细胞化学仅用抗体4H84和HCA2检测到HLA-G2。单克隆抗体16G1仅与转染了HLA-Gsol的细胞系结合。单克隆抗体BFL.1的HLA-G特异性被认为存在疑问,因为它未能与大多数转染了HLA-G的细胞系发生反应。87G与经IFN-γ和GM-CSF刺激的单核细胞或U-937细胞表面的结合是一种Fc受体介导的现象。

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