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10.1021/pr3001332

http://scihub22266oqcxt.onion/10.1021/pr3001332
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C3412919!3412919!22709384
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suck abstract from ncbi


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pmid22709384      J+Proteome+Res 2012 ; 11 (8): 4091-101
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  • Proteome Alterations in Primary Human Alveolar Macrophages in Response to Influenza A Virus Infection #MMPMID22709384
  • Liu L; Zhou J; Wang Y; Mason RJ; Funk CJ; Du Y
  • J Proteome Res 2012[Aug]; 11 (8): 4091-101 PMID22709384show ga
  • In order to obtain a global picture of how alveolar macrophages respond to influenza A virus (IAV) infection, we used a quantitative proteomics method to systematically examine protein expression in the IAV-infected primary human alveolar macrophages. Of the 1214 proteins identified, 43 were significantly up-regulated and 63 significantly down-regulated at > 95% confidence. The expression of an array of interferon (IFN)-induced proteins was significantly increased in the IAV-infected macrophages. The protein with the greatest expression increase was ISG15, an IFN-induced protein that has been shown to play an important role in antiviral defense. Concomitantly, quantitative real time PCR analysis revealed that the gene expression of type I IFNs increased substantially following virus infection. Our results are consistent with the notion that type I IFNs play a vital role in the response of human alveolar macrophages to IAV infection. In addition to the IFN-mediated responses, inflammatory response, apoptosis and redox state rebalancing appeared also to be major pathways that were affected by IAV infection. Furthermore, our data suggest that alveolar macrophages may play a crucial role in regenerating alveolar epithelium during IAV infection.
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