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    Please use this identifier to cite or link to this item: https://ir.csmu.edu.tw:8080/ir/handle/310902500/10819


    Title: Gaseous nitrogen oxides stimulate cell cycle progression by retinoblastoma phosphorylation via activation of cyclins/Cdks [correction].
    Authors: Chen, JH
    Tseng, TH
    Ho, YC
    Lin, HH
    Lin, WL
    Wang, CJ
    Contributors: 中山醫學大學
    Keywords: gaseous nitrogen oxides;proliferation;cdk inhibitor (CKI);Rb phosphorylation;cell cycle progression
    Date: 2003
    Issue Date: 2015-05-15T05:31:07Z (UTC)
    ISSN: 1096-6080
    Abstract: Nitrogen oxides (NOx) are important indoor and outdoor air pollutants. Many studies have indicated that NOx gas causes lung tissue damage by its oxidation properties and its free radicals. In a previous study we demonstrated that NOx gas induced proliferation of human lung fibroblast MRC-5 cells. In this study we show that NOx gas stimulates MRC-5 cell proliferation by retinoblastoma (Rb) phosphorylation via activation of cyclin-cell division protein kinase (cdk) complexes [correction]. Western blot and immunoprecipitation data showed that NOx gas increased the expressions of cyclinA/cdk2, cyclinD1/cdk4, and cyclinE/cdk2 complexes in the cells at 9 h after treatment. The levels of phospho-Rb were also increased and cdk inhibitors (CKIs) p27 and p16 were apparently decreased. These data suggested that NOx gas stimulates cell-cycle progression by Rb phosphorylation via activation of cyclin-cdk complexes and inhibition of CKIs. In conclusion, the NOx-gas that induced lung fibroblast cell proliferation by stimulation of cell-cycle progression may contribute to lung fibrosis by NOx pollutants.
    URI: https://ir.csmu.edu.tw:8080/ir/handle/310902500/10819
    http://dx.doi.org/10.1093/toxsci/kfg221
    Relation: Toxicol Sci. 2003 Nov;76(1):83-90. Epub 2003 Sep 11.
    Appears in Collections:[生化微生物免疫研究所] 期刊論文

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