國家衛生研究院 NHRI:Item 3990099045/10426
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    题名: Functional and biochemical characterization of a T cell-associated anti-apoptotic protein, GIMAP6
    作者: Ho, CH;Tsai, SF
    贡献者: Institute of Molecular and Genomic Medicine
    摘要: GTPases of immunity-associated proteins (GIMAPs) are expressed in lymphocytes and regulate survival/death signaling and cell development within the immune system. We found that human GIMAP6 is expressed primarily in T cell lines. By sorting human peripheral blood mononuclear cells and performing quantitative RT-PCR, GIMAP6 was found to be expressed in CD3+ cells. In Jurkat cells that had been knocked down for GIMAP6, treatment with hydrogen peroxide, FasL or okadaic acid significantly increased cell death/apoptosis. Exogenous expression of GMAP6 protected Huh-7 cells from apoptosis, suggesting that GIMAP6 is an anti-apoptotic protein. Furthermore, knockdown of GIMAP6 not only rendered Jurkat cells sensitive to apoptosis, but also accelerated T cell activation under PMA/ionomycin treatment conditions. Using this experimental system, we also observed a down-regulation of p65 phosphorylation (ser536) in GIMAP6 knockdown cells, indicating that GIMAP6 might display anti-apoptotic function through NF-kappaB activation. The conclusion from the study on cultured T cells was corroborated by the analysis on primary CD3+ T cells showing that specific knockdown of GIMAP6 led to enhancement of PMA/ionomycin-mediated activation signals. To characterize the biochemical properties of GIMAP6, we purified the recombinant GIMAP6 to homogeneity and revealed that GIMAP6 had ATPase as well as GTPase activity. We further demonstrated that the hydrolysis activity of GIMAP6 was not essential for its anti-apoptotic function in Huh-7 cells. Combining the expression data, biochemical properties and cellular features, it is concluded that GIMAP6 plays a role in modulating immune function and does this by controlling cell death and the activation of the T cells.
    日期: 2017-06
    關聯: Journal of Biological Chemistry. 2017 Jun;292(22):9305-9319.
    Link to: http://dx.doi.org/10.1074/jbc.M116.768689
    JIF/Ranking 2023: http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=NHRI&SrcApp=NHRI_IR&KeyISSN=1083-351X&DestApp=IC2JCR
    Cited Times(WOS): https://www.webofscience.com/wos/woscc/full-record/WOS:000402538900025
    Cited Times(Scopus): https://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=85020275403
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