Department of Hematology, The First Affiliated Hospital of University of Science and Technology of China (USTC), The Chinese Academy of Science (CAS) Key Laboratory of Innate Immunity and Chronic Disease, School of Basic Medical Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Institute of Immunology, University of Science and Technology of China, Hefei, China.
Front Immunol. 2023 Mar 3;14:1136652. doi: 10.3389/fimmu.2023.1136652. eCollection 2023.
Human decidual natural killer (dNK) cells are a unique type of tissue-resident NK cells at the maternal-fetal interface. dNK cells are likely to have pivotal roles during pregnancy, including in maternal-fetal immune tolerance, trophoblast invasion, and fetal development. However, detailed insights into these cells are still lacking. In this study, we performed metabolomic and proteomic analyses on human NK cells derived from decidua and peripheral blood. We found that 77 metabolites were significantly changed in dNK cells. Notably, compared to peripheral blood NK (pNK) cells, 29 metabolites involved in glycerophospholipid and glutathione metabolism were significantly decreased in dNK cells. Moreover, we found that 394 proteins were differentially expressed in dNK cells. Pathway analyses and network enrichment analyses identified 110 differentially expressed proteins involved in focal adhesion, cytoskeleton remodeling, oxidoreductase activity, and fatty acid metabolism in dNK cells. The integrated proteomic and metabolomic analyses revealed significant downregulation in glutathione metabolism in dNK cells compared to pNK cells. Our data indicate that human dNK cells have unique metabolism and protein-expression features, likely regulating their function in pregnancy and immunity.
人类蜕膜自然杀伤 (dNK) 细胞是母体-胎儿界面上一种独特的组织驻留 NK 细胞。dNK 细胞在妊娠期间可能具有关键作用,包括母体-胎儿免疫耐受、滋养层浸润和胎儿发育。然而,对这些细胞的详细了解仍然缺乏。在这项研究中,我们对来源于蜕膜和外周血的人 NK 细胞进行了代谢组学和蛋白质组学分析。我们发现 77 种代谢物在 dNK 细胞中发生了显著变化。值得注意的是,与外周血 NK(pNK)细胞相比,dNK 细胞中参与甘油磷脂和谷胱甘肽代谢的 29 种代谢物显著减少。此外,我们发现 394 种蛋白质在 dNK 细胞中差异表达。通路分析和网络富集分析确定了 110 种差异表达蛋白,这些蛋白参与 dNK 细胞中的粘着斑、细胞骨架重塑、氧化还原酶活性和脂肪酸代谢。整合的蛋白质组学和代谢组学分析表明,与 pNK 细胞相比,dNK 细胞中的谷胱甘肽代谢显著下调。我们的数据表明,人类 dNK 细胞具有独特的代谢和蛋白表达特征,可能调节其在妊娠和免疫中的功能。