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HIV-1 gp41结合蛋白和针对gp41的抗体可抑制gp41对人Raji细胞MHC I类和II类分子表达的增强作用。

HIV-1 gp41 binding proteins and antibodies to gp41 could inhibit enhancement of human Raji cell MHC class I and II expression by gp41.

作者信息

Chen Y H, Böck G, Vornhagen R, Steindl F, Katinger H, Dierich M P

机构信息

Ludwig-Boltzmann Institute of AIDS Research, Innsbruck, Austria.

出版信息

Mol Immunol. 1994 Sep;31(13):977-82. doi: 10.1016/0161-5890(94)90092-2.

Abstract

Based on our findings, that HIV-1 soluble gp41 could bind to several proteins on the human, T, B and monocyte cells independently of CD4, we examined the effect of HIV-1 soluble gp41 (sgp41;Env amino acids 539-684) on surface expression of MHC I and II, ICAM-1 and CD21 molecules on human Raji cells. Flow cytometry (FACS) analysis demonstrated that sgp41 could selectively enhance MHC class I and II expression on Raji cells, but did not increase expression of other cell surface antigens, such as, CD21 and CD54 (ICAM-1). Soluble gp41 could also enhance MHC class I and II expression on another human B cell line, Bjab. The sgp41-dependent enhancement of the MHC class I and II expression on Raji cells is time- and dose-dependent. The sgp41 enhancement effect on the MHC antigen expression could be inhibited by the sgp41-binding proteins of 45, 49 and 62 kD (isolated from Raji-lysate) which could inhibit the spg41-binding to Raji cells. Interestingly, this sgp41-dependent enhancement of the MHC class I and II expression could also be inhibited by two mAbs to HIV-1 gp41, but not by a third mAb binding to a different site on gp41. These results demonstrate that HIV-1 sgp41 can selectively enhance the human Raji cell MHC class I and II antigen expression and this enhancement effect could be inhibited by the sgp41-binding proteins and anti-gp41 antibodies, and suggest that the sgp41-dependent enhancement is mediated by its binding to Raji membrane proteins of 45, 49 and 62 kD.

摘要

基于我们的研究发现,即HIV-1可溶性糖蛋白41(gp41)可独立于CD4与人类T细胞、B细胞和单核细胞上的多种蛋白质结合,我们检测了HIV-1可溶性糖蛋白41(sgp41;Env氨基酸539 - 684)对人Raji细胞表面MHC I和II、细胞间黏附分子-1(ICAM-1)及CD21分子表达的影响。流式细胞术(FACS)分析表明,sgp41可选择性增强Raji细胞上MHC I类和II类分子的表达,但不会增加其他细胞表面抗原如CD21和CD54(ICAM-1)的表达。可溶性gp41还可增强另一人B细胞系Bjab上MHC I类和II类分子的表达。sgp41对Raji细胞上MHC I类和II类分子表达的增强作用具有时间和剂量依赖性。sgp41对MHC抗原表达的增强作用可被45、49和62 kD的sgp41结合蛋白(从Raji裂解物中分离)抑制,这些蛋白可抑制spg41与Raji细胞的结合。有趣的是,sgp41对MHC I类和II类分子表达的这种增强作用也可被两种抗HIV-1 gp41单克隆抗体抑制,但不能被结合gp41上不同位点的第三种单克隆抗体抑制。这些结果表明,HIV-1 sgp41可选择性增强人Raji细胞MHC I类和II类抗原的表达,且这种增强作用可被sgp41结合蛋白和抗gp41抗体抑制,提示sgp41依赖性增强作用是由其与45、49和62 kD的Raji膜蛋白结合介导的。

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