西塔
MHC I级
川东北74
生物
抗原处理
与抗原处理相关的转运体
MHC II级
主要组织相容性复合体
C-C趋化因子受体7型
抗原呈递
染色质免疫沉淀
细胞生物学
分子生物学
发起人
基因表达
遗传学
抗原
T细胞
基因
免疫系统
趋化因子
趋化因子受体
作者
Torsten Meißner,Amy Li,Amlan Biswas,Kyoung‐Hee Lee,Yuen-Joyce Liu,Erkan Bayir,Dimitrios Iliopoulos,Peter J. van den Elsen,Koichi S. Kobayashi
标识
DOI:10.1073/pnas.1008684107
摘要
MHC class I plays a critical role in the immune defense against viruses and tumors by presenting antigens to CD8 T cells. An NLR protein, class II transactivator (CIITA), is a key regulator of MHC class II gene expression that associates and cooperates with transcription factors in the MHC class II promoter. Although CIITA also transactivates MHC class I gene promoters, loss of CIITA in humans and mice results in the severe reduction of only MHC class II expression, suggesting that additional mechanisms regulate the expression of MHC class I. Here, we identify another member of the NLR protein family, NLRC5, as a transcriptional regulator of MHC class I genes. Similar to CIITA, NLRC5 is an IFN-gamma-inducible nuclear protein, and the expression of NLRC5 resulted in enhanced MHC class I expression in lymphoid as well as epithelial cell lines. Using chromatin immunoprecipitation and reporter gene assays, we show that NLRC5 associates with and activates the promoters of MHC class I genes. Furthermore, we show that the IFN-gamma-induced up-regulation of MHC class I requires NLRC5, because knockdown of NLRC5 specifically impaired the expression of MHC class I. In addition to MHC class I genes, NLRC5 also induced the expression of beta2-microglobulin, transporter associated with antigen processing, and large multifunctional protease, which are essential for MHC class I antigen presentation. Our results suggest that NLRC5 is a transcriptional regulator, orchestrating the concerted expression of critical components in the MHC class I pathway.
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