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首页> 外文期刊>Virology >Endogenously expressed HIV-1 nef down-regulates antigen-presenting molecules, not only class I MHC but also CD1a, in immature dendritic cells.
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Endogenously expressed HIV-1 nef down-regulates antigen-presenting molecules, not only class I MHC but also CD1a, in immature dendritic cells.

机译:内源性表达的HIV-1 nef下调了未成熟树突状细胞中的抗原呈递分子,不仅是I类MHC,而且还下调了CD1a。

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摘要

The effects of Nef molecules on immature dendritic cells (iDCs) were analyzed using recombinant human immunodeficiency virus type 1 (HIV-1) with intact nef gene, pseudotyped with vesicular stomatitis virus glycoprotein, HIV/VSV-G/+Nef. When iDCs were infected with HIV/VSV-G/+Nef, the surface expression of CD1a, a molecule for presenting glycolipid/lipid antigens, was selectively down-regulated among CD1 molecules (CD1a, -b, -c, and -d) as well as class I MHC. Moreover, the CD1a molecules were also down-modulated and co-localized with DsRed2-tagged-Nef in CD1a-transfected cells. Their co-localization was dependent upon CD1a cytoplasmic tail and the CD1a was redistributed from cell surface to LAMP-1+ late endosomal/lysosomal compartment. These findings reveal that the HIV-1-Nef interferes with the intracellular trafficking of CD1a, and suggest the involvement of CD1a-restricted immune effectors in the protective immunity against HIV-1 infection, which implicates the feasibility of virus-derived glycolipid/lipid antigens together with epitope peptides for the vaccine development.
机译:使用具有完整nef基因的重组人免疫缺陷病毒1型(HIV-1)(用水泡性口炎病毒糖蛋白HIV / VSV-G / + Nef假型)重组Nef分子对未成熟树突状细胞(iDC)的作用进行了分析。当iDC感染HIV / VSV-G / + Nef时,在CD1分子(CD1a,-b,-c和-d)中选择性下调了呈递糖脂/脂抗原的分子CD1a的表面表达。以及I类MHC。此外,在CD1a转染的细胞中,CD1a分子也被下调并与DsRed2-tagged-Nef共定位。它们的共定位取决于CD1a胞质尾巴,并且CD1a从细胞表面重新分布到LAMP-1 +内体/溶酶体晚期区室。这些发现表明,HIV-1-Nef干扰了CD1a的细胞内运输,并暗示了受CD1a限制的免疫效应子参与了针对HIV-1感染的保护性免疫,这暗示了病毒衍生的糖脂/脂质抗原的可行性与表位肽一起用于疫苗开发。

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