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Functional Competence of NK Cells via the KIR/MHC Class I Interaction Correlates with DNAM-1 Expression

NKG2D公司 MHC I级 白细胞介素21 德纳姆 人类白细胞抗原 生物 免疫学 淋巴因子激活杀伤细胞 细胞生物学 主要组织相容性复合体 白细胞介素12 受体 体外 细胞毒性T细胞 T细胞 抗原 免疫系统 基因表达 生物化学 DNA甲基化 基因
作者
Qian‐Nan Shang,Xingxing Yu,Zhengli Xu,Xunhong Cao,Xuefei Liu,Xiaosu Zhao,Ying‐Jun Chang,Yu Wang,Xiaohui Zhang,Lan‐Ping Xu,Kai‐Yan Liu,Xiao‐Jun Huang,Xiaosu Zhao
出处
期刊:Journal of Immunology [American Association of Immunologists]
卷期号:208 (2): 492-500 被引量:13
标识
DOI:10.4049/jimmunol.2100487
摘要

Abstract The interaction of inhibitory receptors with self–MHC class I (MHC-I) molecules is responsible for NK cell education. The intensity of DNAM-1 expression correlates with NK cell education. However, whether DNAM-1 expression directly influences the functional competence of NK cells via the KIR/MHC-I interaction remains unclear. Based on allogeneic haploidentical hematopoietic stem cell transplantation, we investigated the intensity of DNAM-1 expression on reconstituted NK cells via the interaction of KIR with both donor HLA and recipient HLA at days 30, 90, and 180 after hematopoietic stem cell transplantation. The reconstituted NK cells educated by donor and recipient HLA molecules showed the highest DNAM-1 expression, whereas DNAM-1 expression on educated NK cells with only recipient HLA molecules was higher than that on educated NK cells with only donor HLA molecules, indicating that NK cells with donor or recipient HLA molecules regulate DNAM-1 expression and thereby affect NK cell education. Additionally, the effects of recipient cells on NK cell education were greater than those of donor cells. However, only when the DNAM-1, NKP30, and NKG2D receptors were blocked simultaneously was the function of educated and uneducated NK cells similar. Therefore, activating receptors may collaborate with DNAM-1 to induce educated NK cell hyperresponsiveness. Our data, based on in vitro and in vivo studies, demonstrate that the functional competence of NK cells via the KIR/MHC-I interaction correlates with DNAM-1 expression in human NK cells.
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