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首页> 外文期刊>Virus Research: An International Journal of Molecular and Cellular Virology >Differences in Env and Gag protein expression patterns and epitope availability in feline immunodeficiency virus infected PBMC compared to infected and transfected feline model cell lines
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Differences in Env and Gag protein expression patterns and epitope availability in feline immunodeficiency virus infected PBMC compared to infected and transfected feline model cell lines

机译:与感染和转染的猫培养基细胞系相比,猫免疫缺陷病毒感染PBMC的Env和Gag蛋白表达模式和表位可用性的差异

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摘要

Env and Gag are key components of the FIV virion that are targeted to the plasma membrane for virion assembly. They are both important stimulators and targets of anti-FIV immunity. To investigate and compare the expression pattern and antigenic changes of Gag and Env in various research models, infected PBMC (the natural FIV host cells) and GFox, and transfected CrFK were stained over time with various Env and Gag specific MAbs. In FIV infected GFox and PBMC, Env showed changes in epitope availability for antibody binding during processing and trafficking, which was not seen in transfected CrFK. Interestingly, epitopes exposed on intracellular Env and Env present on the plasma membrane of CrFK and GFox seem to be hidden on plasma membrane expressed Env of FIV infected PBMC. A kinetic follow up of Gag and Env expression showed a polarization of both Gag and Env expression to specific sites at the plasma membrane of PBMC, but not in other cell lines. In conclusion, mature trimeric cell surface expressed Env might be antigenically distinct from intracellular monomeric Env in PBMC and might possibly be unrecognizable by feline humoral immunity. In addition, Env expression is restricted to a small area on the plasma membrane and co-localizes with a large moiety of Gag, which may represent a preferred FIV budding site, or initiation of virological synapses with direct cell-to-cell virus transmission. (C) 2016 Published by Elsevier B.V.
机译:ENV和GAG是FIV病毒粒子的关键组分,其靶向VAIRION组装的质膜。它们都是重要的刺激者和抗FIV免疫的目标。为了调查和比较GAG和ENV在各种研究模型中的表达模式和抗原变化,感染PBMC(天然FIV宿主细胞)和GFOX,并随着各种env和GAG特异性mAb染色随时间染色的转染的CRFK。在FIV感染的GFOX和PBMC中,ENV显示出在处理和贩运过程中抗体结合的表位可用性的变化,在转染的CRFK中未见。有趣的是,暴露于CRFK和GFOX的质膜细胞内ENV和ENV的表位似乎隐藏在FIV感染PBMC的血浆膜上。 Gag和Env表达的动力学跟随显示出Gag和Env表达的偏振,在PBMC的质膜上的特定位点,但不在其他细胞系中。总之,成熟三聚体细胞表面表达的ENV可能与PBMC中细胞内单体engerbellulic eng中的抗原性不同,并且可能因猫的体液免疫而无法辨认。此外,Env表达限于血浆膜上的一小部分,并用大量的GAG共定位,其可以代表优选的FIV萌芽位点,或者具有直接细胞对细胞病毒透射的病毒学突触的开始。 (c)2016年由Elsevier B.V发布。

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