ASIA unversity:Item 310904400/16936
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    Please use this identifier to cite or link to this item: http://asiair.asia.edu.tw/ir/handle/310904400/16936


    Title: Correlation between TGF beta-1 expression and proteomic profiling induced by SARS coronavirus papain like-protease
    Authors: 林振文;LIN, CHENG-WEN
    Contributors: 生物科技學系
    Date: 2012-09
    Issue Date: 2012-11-23 17:18:37 (UTC+8)
    Abstract: Severe acute respiratory syndrome (SARS) coronavirus (SARS-CoV) papain-like protease (PLpro), a deubiquitinating enzyme, demonstrates inactivation of interferon (IFN) regulatory factor 3 and NF-κB, reduction of IFN induction, and suppression of type I IFN signaling pathway. This study investigates cytokine expression and proteomic change induced by SARS-CoV PLpro in human promonocyte cells. PLpro significantly increased TGF-β1 mRNA expression (greater than fourfold) and protein production (greater than threefold). Proteomic analysis, Western blot, and quantitative real-time PCR assays indicated PLpro upregulating TGF-β1-associated genes: HSP27, protein disulfide isomerase A3 precursor, glial fibrillary acidic protein, vimentin, retinal dehydrogenase 2, and glutathione transferase omega-1. PLpro-activated ubiquitin proteasome pathway via upregulation of ubiquitin-conjugating enzyme E2-25k and proteasome subunit alpha type 5. Proteasome inhibitor MG-132 significantly reduced expression of TGF-β1 and vimentin. PLpro upregulated HSP27, linking with activation of p38 MAPK and ERK1/2 signaling. Treatment with SB203580 and U0126 reduced PLpro-induced expression of TGF-β1, vimentin, and type I collagen. Results point to SARS-CoV PLpro triggering TGF-β1 production via ubiquitin proteasome, p38 MAPK, and ERK1/2-mediated signaling.
    © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
    Relation: PROTEOMICS;12(21):3193-205.
    Appears in Collections:[Department of Biotechnology] Journal Article

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