Cell Res.：NLRC5在抗感染免疫研究中起关键作用

李斯特菌(L. monocytogenes)扫描电子显微图片，图片来自维基共享资源。

真核生物的天然免疫是抵抗外界病原体入侵的第一道防线。天然免疫主要是通过模式识别受体来识别病毒或细菌等外来病原体。Nod样受体（NLR）是近年来研究发现的识别胞内菌的模式受体。NLRC5作为Nod样受体家族中最大的一个成员，其生理学功能一直不清楚。

4月10号，Cell Research杂志在线发表中科院上海生命科学研究院/上海交通大学医学院健康科学研究所钱友存研究组关于NLRC5在抗胞内菌感染过程中的作用研究 (NLRC5 regulates MHC class I antigen presentation in host defense against intracellular pathogens)。该工作主要由博士生姚依昆和王亚龙在钱友存研究员的指导下完成。该论文首次利用NLRC5基因敲除小鼠研究发现NLRC5在宿主抵抗胞内菌感染方面发挥重要作用。NLRC5通过调控I类主要组织相容性复合体（MHC class I）的转录表达，进而影响胞内病原菌（李斯特菌，L. monocytogenes）特异性CD8＋ T细胞的激活和增殖，从而有效清除病原菌。该研究阐明了宿主抗胞内菌感染的新机制，为感染性疾病的预防与治疗提供了重要的理论基础。

该课题获得国家自然科学基金委、国家科技部、中国科学院和上海市科委等经费资助。

doi:10.1038/cr.2012.56
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NLRC5 regulates MHC class I antigen presentation in host defense against intracellular pathogens

Yikun Yao, Yalong Wang, Fuxiang Chen, Yin Huang, Shu Zhu, Qibin Leng, Hongyan Wang, Yufang Shi and Youcun Qian

NOD-like receptors (NLRs) are a family of intracellular proteins that play critical roles in innate immunity against microbial infection. NLRC5, the largest member of the NLR family, has recently attracted much attention. However, in vitro studies have reported inconsistent results about the roles of NLRC5 in host defense and in regulating immune signaling pathways. The in vivo function of NLRC5 remains unknown. Here, we report that NLRC5 is a critical regulator of host defense against intracellular pathogens in vivo. NLRC5 was specifically required for the expression of genes involved in MHC class I antigen presentation. NLRC5-deficient mice showed a profound defect in the expression of MHC class I genes and a concomitant failure to activate L. monocytogenes-specific CD8+ T cell responses, including activation, proliferation and cytotoxicity, and the mutant mice were more susceptible to the pathogen infection. NLRP3-mediated inflammasome activation was also partially impaired in NLRC5-deficient mice. However, NLRC5 was dispensable for pathogen-induced expression of NF-κB-dependent pro-inflammatory genes as well as type I interferon genes. Thus, NLRC5 critically regulates MHC class I antigen presentation to control intracellular pathogen infection.