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대한생화학·분자생물학회 Experimental and Molecular Medicine Experimental and Molecular Medicine 제46권
발행연도
2014.1
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1 - 9 (9page)

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Redox-regulating molecule, recombinant human thioredoxin (rhTRX) which shows anti-inflammatory, and anti-oxidative effectsagainst lipopolysaccharide (LPS)-stimulated inflammation and regulate protein expression levels. LPS-induced reactive oxygenintermediates (ROI) and NO production were inhibited by exogenous rhTRX. We identified up/downregulated intracellularproteins under the LPS-treated condition in exogenous rhTRX-treated A375 cells compared with non-LPS-treated cells via 2-DEproteomic analysis. Also, we quantitatively measured cytokines of in vivo mouse inflammation models using cytometry beadarray. Exogenous rhTRX inhibited LPS-stimulated production of ROI and NO levels. TIP47 and ATP synthase may influencethe inflammation-related lipid accumulation by affecting lipid metabolism. The modulation of skin redox environments duringinflammation is most likely to prevent alterations in lipid metabolism through upregulation of TIP47 and ATP synthase anddownregulation of inflammatory cytokines. Our results demonstrate that exogenous rhTRX has anti-inflammatory propertiesand intracellular regulatory activity in vivo and in vitro. Monitoring of LPS-stimulated pro-inflammatory conditions treated withrhTRX in A375 cells could be useful for diagnosis and follow-up of inflammation reduction related with candidate proteins. These results have a therapeutic role in skin inflammation therapy.

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