Endoplasmic reticulum stress induced LOX‐1+ CD 15+ polymorphonuclear myeloid‐derived suppressor cells in hepatocellular carcinoma

作者：Jiang Nan, Yan‐Fang Xing, Bo Hu, Jianxin Tang, Huimin Dong, Yu‐Mei He, Dan‐Yun Ruan, Qing‐Jian Ye, Jia‐Rong Cai, Xiaokun Ma, Jie Chen, Xiurong Cai, Ze‐Xiao Lin, Xiangyuan Wu, Xing Li · 发表于：Immunology · 年份：2017 · DOI：10.1111/imm.12876 · 被引用次数：114 · 研究领域：Immune cells in cancer、Immune Cell Function and Interaction、Sphingolipid Metabolism and Signaling

Summary A recent study indicated that Lectin‐type oxidized LDL receptor‐1 (LOX‐1) was a distinct surface marker for human polymorphisms myeloid‐derived suppressor cells (PMN‐MDSC). The present study was aimed to investigate the existence LOX‐1 PMN‐MDSC in hepatocellular carcinoma (HCC) patients. One hundred and twenty‐seven HCC patients, 10 patients with mild active chronic hepatitis B, 10 liver cirrhosis due to hepatitis B, 10 liver dysplastic node with hepatitis B and 50 health control were included. LOX‐1 + CD15 + PMN‐MDSC were significantly elevated in HCC patients compared with healthy control and patients with benign diseases. LOX‐1 + CD15 + PMN‐MDSC in circulation were positively associated with those in HCC tissues. LOX‐1 + CD15 + PMN‐MDSCs significantly reduced proliferation and IFN‐ γ production of T cells with a dosage dependent manner with LOX‐1 − CD15 + PMNs reached negative results. The suppression on T cell proliferation and IFN‐ γ production was reversed by ROS inhibitor and Arginase inhibitor. ROS level and activity of arginase of LOX‐1 + CD15 + PMN were higher in LOX‐1 + CD15 + PMN‐MDSCs than LOX‐1 − CD15 + PMNs, as well as the expression of the NADPH oxidase NOX2 and arginase I. RNA sequence revealed that LOX‐1 + CD15 + PMN‐MDSCs displayed significantly higher expression of spliced X‐box ‐binding protein 1 (sXBP1), an endoplasmic reticulum (ER) stress marker. ER stress inducer induced LOX‐1 expression and suppressive function for CD15 + PMN from health dono...