Hydroxychloroquine inhibiting neutrophil extracellular trap formation alleviates hepatic ischemia/reperfusion injury by blocking TLR9 in mice

被引:58
作者
Zhang, Sigong [1 ]
Zhang, Qiuyue [2 ]
Wang, Furong [3 ]
Guo, Xuehui [4 ]
Liu, Tao [5 ]
Zhao, Yang [5 ]
Gu, Baohong [2 ]
Chen, Hao [5 ]
Li, Yumin [5 ]
机构
[1] Lanzhou Univ, Dept Rheumatol, Key Lab Digest Syst Tumors Gansu Prov, Hosp 2, Lanzhou, Gansu, Peoples R China
[2] Lanzhou Univ, Clin Med Coll 2, Lanzhou, Gansu, Peoples R China
[3] Lanzhou Univ, Dept Pathol, Hosp 2, Lanzhou, Gansu, Peoples R China
[4] Gansu Emergency Med Aid Ctr, Lanzhou, Gansu, Peoples R China
[5] Lanzhou Univ, Key Lab Digest Syst Tumors Gansu Prov, Hosp 2, Lanzhou, Gansu, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
REPERFUSION INJURY; LIVER; RECEPTOR; MECHANISM; ISCHEMIA;
D O I
10.1016/j.clim.2020.108461
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Hepatic ischemia/reperfusion (I/R) injury may arise after partial hepatectomy and liver transplantation. Neutrophil extracellular traps (NETs) were involved in hepatic I/R injury. This study tested the hypothesis that blocking NETs formation could be a potential therapeutic target against hepatic I/R injury. NETs were excessively formed within liver and in serum of I/R mice models and were testified to be an independent contributor to hepatic I/R injury. Hydroxychloroquine (HCQ) alleviated hepatic I/R injury by inhibiting NETs formation in SCID and c57BL/6 mice models. In vitro, HCQ inhibited neutrophils to form NETs at a concentration of 100 mu g/ml. CpG-ODN reversed the effect of HCQ inhibiting NETs formation. HCQ inhibited PAD4 and Rac2 expressions by blocking TLR9. NETs are essential contributors to hepatic I/R injury. HCQ blocking TLR9 protects against hepatic I/R injury by inhibiting NETs formation, which may suggest utility of HCQ or other TLR9 agonists for preventing hepatic I/R injury in clinical practices.
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页数:10
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