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Molecular Cell:中山大学崔隽、黄军就发表天然免疫的调控机理新研究

2016-10-01 王英 生物通

近期,中山大学的两位80后教授崔隽(Jun Cui)、黄军就(Jun-Jiu Huang)联手美国康奈尔威尔医学院“微生物学和免疫学”教授、休斯顿卫理公会医院研究所炎症和表观遗传学中心主任王荣福(Rong-Fu Wang)教授,在国际学术期刊《Molecular Cell》在线发表了题为“TRIM14 Inhibits cGAS Degradation Mediated by Selective


近期,中山大学的两位80后教授崔隽(Jun Cui)、黄军就(Jun-Jiu Huang)联手美国康奈尔威尔医学院“微生物学和免疫学”教授、休斯顿卫理公会医院研究所炎症和表观遗传学中心主任王荣福(Rong-Fu Wang)教授,在国际学术期刊《Molecular Cell》在线发表了题为“TRIM14 Inhibits cGAS Degradation Mediated by Selective Autophagy Receptor p62 to Promote Innate Immune Responses”的学术成果,这篇论文主要讲述了有关天然免疫的调控机理。

崔隽教授长期从事固有免疫系统识别和调控、信号转导机制与疾病相关性研究,在Cell, Immunity, Nature immunology等顶级杂志发表了多项重要的研究论文。王荣福教授的主要研究方向包括肿瘤抗原鉴定、先天免疫、肿瘤免疫治疗,以及干细胞和肿瘤的表观遗传调节。王荣福教授目前担任炎症和表观遗传学中心主任及教授、糖尿病研究中心主任。他在肿瘤抗原鉴定、先天免疫、肿瘤免疫治疗,以及干细胞和肿瘤的表观遗传调节方面有着长期稳定的研究兴趣。

环GMP-AMP合成酶(cGAS)是一种重要的DNA病毒传感器,可通过触发I型干扰素(IFN)信号产生cGAMP,而启动病毒免疫反应。然而,cGAS的转录后调控仍是未知的。在这项新的研究中,研究人员报道称,cGAS的K48-连接泛素化是依赖于p62的选择性自噬降解的一种识别信号。I型干扰素能够诱导TRIM14的生产,进而通过招募USP14来切割赖氨酸(K)414上的cGAS泛素链,而促进cGAS的稳定性。

敲除TRIM14可以一种cGAS依赖性的方式,损害单纯疱疹病毒1型(HSV-1)引发的抗病毒反应。由于产生I型IFN的能力显著削弱,Trim14−/−小鼠对于致死性HSV-1感染是高度敏感的。总之,这些研究结果揭示了TRIM14-USP14产生的一种cGAS信号正反馈回路,并对天然免疫中自噬与I型IFN信号之间的串扰,提供了新的见解。

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    2017-01-07 维他命
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    2016-10-15 inter158

    80后教授很厉害

    0

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    2016-10-02 医路开来

    谢谢分享,,,

    0

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    2016-10-02 医路开来

    学习啦,,,

    0

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    2016-10-02 萌面超人

    ?

    0

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    2016-10-02 刘煜

    学习了谢谢。

    0

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