Nikopaschou Martha, Samiotaki Martina, Stylianaki Elli-Anna, Król Kamila, Gragera Paula, Raja Aroosha, Aidinis Vassilis, Chroni Angeliki, Fruci Doriana, Panayotou George, Stratikos Efstratios
National Centre for Scientific Research Demokritos, Agia Paraskevi, Greece; Department of Chemistry, National and Kapodistrian University of Athens, Zografou, Greece.
Biomedical Sciences Research Center "Alexander Fleming", Institute for Bioinnovation, Vari, Greece.
Mol Cell Proteomics. 2025 May;24(5):100964. doi: 10.1016/j.mcpro.2025.100964. Epub 2025 Apr 4.
Endoplasmic reticulum (ER) aminopeptidase 1 (ERAP1) metabolizes peptides inside the ER and shapes the peptide repertoire available for binding to major histocompatibility complex class I molecules (MHC-I). However, it may have additional effects on cellular homeostasis, which have not been explored. To address these questions, we used both genetic silencing of ERAP1 expression as well as treatment with a selective allosteric ERAP1 inhibitor to probe changes in the immunopeptidome and proteome of the A375 melanoma cancer cell line. We observed significant immunopeptidome shifts with both methods of functional ERAP1 disruption, which were distinct for each method. Both methods of inhibition led to an enhancement, albeit slight, in tumor cell killing by stimulated human peripheral blood mononuclear cells and in significant proteomic alterations in pathways related to metabolism and cellular stress. Similar proteomic changes were also observed in the leukemia cell line THP-1. Biochemical analyses suggested that ERAP1 inhibition affected sensitivity to ER stress, reactive oxygen species production, and mitochondrial metabolism. Although the proteomics shifts were significant, their potential in shaping immunopeptidome shifts was limited since only 9.6% of differentially presented peptides belonged to proteins with altered expression and only 4.0% of proteins with altered expression were represented in the immunopeptidome shifts. Taken together, our findings suggest that modulation of ERAP1 activity can generate unique immunopeptidomes, mainly due to altered peptide processing in the ER, but also induce changes in the cellular proteome and metabolic state which may have further effects on tumor cells.
内质网(ER)氨肽酶1(ERAP1)在内质网内代谢肽,并塑造可用于与主要组织相容性复合体I类分子(MHC-I)结合的肽库。然而,它可能对细胞稳态有其他影响,而这尚未得到探索。为了解决这些问题,我们使用了ERAP1表达的基因沉默以及用选择性变构ERAP1抑制剂进行处理,以探究A375黑色素瘤癌细胞系的免疫肽组和蛋白质组的变化。我们观察到,通过这两种功能性ERAP1破坏方法,免疫肽组都发生了显著变化,且每种方法的变化都不同。两种抑制方法都导致受刺激的人外周血单核细胞对肿瘤细胞的杀伤作用略有增强,以及与代谢和细胞应激相关途径中的蛋白质组发生显著改变。在白血病细胞系THP-1中也观察到了类似的蛋白质组变化。生化分析表明,ERAP1抑制影响了对内质网应激的敏感性、活性氧的产生和线粒体代谢。尽管蛋白质组学的变化很显著,但它们在塑造免疫肽组变化方面的潜力有限,因为只有9.6%的差异呈现肽属于表达改变的蛋白质,且免疫肽组变化中仅4.0%的表达改变蛋白质有所体现。综上所述,我们的研究结果表明,ERAP1活性的调节可以产生独特的免疫肽组,这主要是由于内质网中肽加工的改变,但也会诱导细胞蛋白质组和代谢状态的变化,这可能对肿瘤细胞产生进一步影响。