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p53 increases MHC class I expression by upregulating the endoplasmic reticulum aminopeptidase ERAP1

机译:p53通过上调内质网氨基肽酶ERAP1增加MHC I类表达

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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.
机译:p53抑癌药在癌细胞中具有重要作用。在这里,我们显示p53调节细胞表面主要组织相容性复合体I的表达。我们显示,缺乏p53的肿瘤细胞系HCT116表现出比其野生型对应物低得多的主要组织相容性复合物I表达。使用染色质免疫沉淀测序和基因表达分析的组合,我们证明p53通过与ERAP1基因中的同源应答元件结合来上调内质网氨基肽酶1的表达。 p53沉默会降低内质网氨基肽酶1的蛋白质水平,从而降低主要的组织相容性复合体I的表达。我们进一步表明,这种机制在感染H1N1流感病毒的A549细胞中起作用,其中H1N1激活p53,导致内质网氨基肽酶1上调并在主要组织相容性复合体I表达上相应增加。我们的研究表明,p53功能与癌症和感染的免疫监视之间以前没有被认识的联系。

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