Singapore Immunology Network, A*STAR, 8A Biomedical Grove, Singapore 138648, Singapore.
Nat Commun. 2013;4:2359. doi: 10.1038/ncomms3359.
The p53 tumour suppressor has an important role in cancer cells. Here we show that p53 regulates expression of major histocompatibility complex I on the cell surface. We show that the tumour cell line HCT116, which lacks p53 exhibits significantly lower major histocompatibility complex I expression than its wild-type counterpart. Using a combination of chromatin immunoprecipitation sequencing and gene expression analysis, we demonstrate that p53 upregulates expression of endoplasmic reticulum aminopeptidase 1 by binding to its cognate response element in the ERAP1 gene. Silencing of p53 decreases endoplasmic reticulum aminopeptidase 1 protein levels and therefore major histocompatibility complex I expression. We further show that this mechanism operates in A549 cells infected with H1N1 influenza virus, in which H1N1 activates p53, leading to endoplasmic reticulum aminopeptidase 1 upregulation and a corresponding increase in major histocompatibility complex I expression. Our study suggests a previously unrecognized link between p53 function and the immunosurveillance of cancer and infection.
p53 肿瘤抑制因子在癌细胞中具有重要作用。在这里,我们表明 p53 调节细胞表面主要组织相容性复合体 I 的表达。我们表明,缺乏 p53 的肿瘤细胞系 HCT116 表现出明显低于其野生型对应物的主要组织相容性复合体 I 表达。通过结合染色质免疫沉淀测序和基因表达分析,我们证明 p53 通过结合 ERAP1 基因中其同源反应元件来上调内质网氨肽酶 1 的表达。沉默 p53 会降低内质网氨肽酶 1 蛋白水平,从而降低主要组织相容性复合体 I 的表达。我们进一步表明,在感染 H1N1 流感病毒的 A549 细胞中,该机制起作用,其中 H1N1 激活 p53,导致内质网氨肽酶 1 上调,并相应增加主要组织相容性复合体 I 的表达。我们的研究表明,p53 功能与癌症和感染的免疫监视之间存在以前未被认识到的联系。