首页> 美国卫生研究院文献>The Journal of Experimental Medicine >LMP-associated proteolytic activities and TAP-dependent peptide transport for class 1 MHC molecules are suppressed in cell lines transformed by the highly oncogenic adenovirus 12
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LMP-associated proteolytic activities and TAP-dependent peptide transport for class 1 MHC molecules are suppressed in cell lines transformed by the highly oncogenic adenovirus 12

机译:LMP相关的蛋白水解活性和1类MHC分子的TAP依赖性肽运输在高致癌性腺病毒转化的细胞系中受到抑制12

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摘要

Expression of class I major histocompatibility complex antigens on the surface of cells transformed by adenovirus 12 (Ad12) is generally very low, and correlates with the in vivo oncogenicity of this virus. In primary embryonal fibroblasts (H-2b) that express transgenic swine class I antigen (PD1), Ad12-mediated transformation results in inhibition in transport of newly synthesized class I molecules, as well as significant reduction in transporter associated with antigen presentation (TAP) gene expression. In this report we show that reexpression of TAP molecules either by stable transfection of mouse TAP genes or by infection with recombinant vaccinia viruses expressing human TAP genes, only partially reconstitutes the expression and transport of the class I molecules. Further analysis of Ad12- transformed cells revealed that the expression of both LMP2 and LMP7, but not of other proteasome complex components, was downregulated, resulting in altered proteolytic activities of the 20S proteasomes. Reconstitution of both TAP and LMP expression resulted in complete restoration of PD1 cell surface expression and enhanced expression of the endogenous H-2D(b) molecules encoded by recombinant vaccinia viruses, in reconstituted Ad12-transformed cells, efficient transport of H-2 class I molecules could only be achieved by treatment of the cells with gamma-interferon. These data suggest that an additional factor(s) that is interferon-regulated plays a role in the biosynthetic pathway of the class I complex, and that its function is deficient in this cell system. Thus, Ad12 viral transformation appears to suppress the expression of multiple genes that are important for antigen processing and presentation, which allows such transformed cells to escape immune surveillance. This coordinate downregulation of immune response genes must likely occur through their use of common regulatory elements.
机译:I类主要组织相容性复合抗原在腺病毒12(Ad12)转化的细胞表面上的表达通常很低,并且与这种病毒的体内致癌性相关。在表达转基因猪I类抗原(PD1)的初级胚胎成纤维细胞(H-2b)中,Ad12介导的转化可抑制新合成的I类分子的转运,并显着减少与抗原呈递相关的转运蛋白(TAP)基因表达。在本报告中,我们表明,通过稳定转染小鼠TAP基因或感染表达人TAP基因的重组痘苗病毒,TAP分子的重新表达只能部分重构I类分子的表达和运输。对Ad12转化的细胞的进一步分析表明,LMP2和LMP7的表达均被下调,而其他蛋白酶体复合物的表达均未下调,从而导致20S蛋白酶体的蛋白水解活性改变。 TAP和LMP表达的重建导致PD1细胞表面表达的完全恢复,重组痘苗病毒编码的内源性H-2D(b)分子在重组的Ad12转化细胞中的表达增强,H-2 I类的有效转运分子只能通过用γ-干扰素处理细胞来实现。这些数据表明,受干扰素调节的其他因子在I类复合物的生物合成途径中起作用,并且其功能在该细胞系统中不足。因此,Ad12病毒转化似乎抑制了对抗原加工和呈递很重要的多个基因的表达,这使得这种转化的细胞能够逃脱免疫监视。免疫应答基因的这种协调下调可能必须通过使用共同的调节元件而发生。

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