國家衛生研究院 NHRI:Item 3990099045/5202
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    Please use this identifier to cite or link to this item: http://ir.nhri.org.tw/handle/3990099045/5202


    Title: The adaptor protein SH2B1Beta reduces hydrogen peroxide-induced cell death in PC12 cells and hippocampal neurons
    Other Titles: The adaptor protein SH2B1β reduces hydrogen peroxide-induced cell death in PC12 cells and hippocampal neurons
    Authors: Lu, WC;Chen, CJ;Hsu, HC;Hsu, HL;Chen, L
    Contributors: Division of Molecular and Genomic Medicine
    Abstract: Background: SH2B1β is a signaling adaptor protein that has been shown to promote neuronal differentiation in PC12 cells and is necessary for the survival of sympathetic neurons. However, the mechanism by which SH2B1β may influence cell survival is not known.Results: In this study, we investigated the role of SH2B1β in oxidative stress-induced cell death. Our results suggest that overexpressing SH2B1β reduced H2O2-induced, caspase 3-dependent apoptosis in PC12 cells and hippocampal neurons. In response to H2O2, overexpressing SH2B1β enhanced PI3K (phosphatidylinositol 3-kinas)- AKT (protein kinase B) and MEK (MAPK/ERK kinase)-extracellular-signal regulated kinases 1 and 2 (ERK1/2) signaling pathways. We further demonstrated that SH2B1β was able to reduce H2O2-induced nuclear localization of FoxO1 and 3a transcription factors, which lie downstream of PI3K-AKT and MEK-ERK1/2 pathways. Moreover, overexpressing SH2B1β reduced the expression of Fas ligand (FasL), one of the target genes of FoxOs. Conclusions: Overexpressing the adaptor protein SH2B1β enhanced H2O2-induced PI3K-AKT and MEK-ERK1/2 signaling, reduced nucleus-localized FoxOs and the expression of a pro-apoptotic gene, FasL.
    Date: 2010-09-27
    Relation: Journal of Molecular Signaling. 2010 Sep;5:Article number 17.
    Link to: http://dx.doi.org/10.1186/1750-2187-5-17
    Cited Times(Scopus): http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=77957118047
    Appears in Collections:[Hsin-Ling Hsu] Periodical Articles

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