Involvement of natural killer cells in PolyI:C-induced liver injury

被引:88
作者
Dong, ZJ
Wei, HM
Sun, R
Hu, ZQ
Gao, B
Tian, ZG
机构
[1] Univ Sci & Technol China, Sch Life Sci, Hefei 230027, Anhui, Peoples R China
[2] Shandong Univ, Sch Pharm, Shandong 250012, Peoples R China
[3] Showa Univ, Sch Med, Dept Microbiol & Immunol, Shinagawa Ku, Tokyo 1428555, Japan
[4] NIAAA, Sect Liver Biol, Lab Physiol Studies, NIH, Bethesda, MD 20892 USA
关键词
liver injury; inflammation; VCAM-1; interleukin; 12; natural killer cells;
D O I
10.1016/j.jhep.2004.08.021
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: The roles of T cells, natural killer T cells (NKT) and macrophages in autoimmune hepatitis have been well documented. However, the roles of natural killer (NK) cells in liver injury remain obscure. Here we examined the effect of Polyinosinic: polycytidylic acid (PolyI:C)-activated NK cells on liver injury. Methods: Mice were intraperitoneally injected with PolyI:C at a dose of 20 mug/g body wt. The percentage and absolute number of NK cells in the liver were analyzed with flow cytometry. Serum alanine transaminase (ALT) and aspartate aminotransferase (AST) assay and H-E staining were used to evaluate the liver injury. Results: Following PolyI:C injection, NK cells accumulation and activation occurred in the liver. Meanwhile, slight elevation of ALT/AST in the serum, mild inflammation and focal necrosis in the liver were also observed. Depletion of NK cells markedly attenuated PolyI:C-induced liver injury. Neutralization of endogenous Interleukin-12 produced by Kupffer cells abrogated the accumulation of NK cells in the liver and subsequent liver injury. The liver injury was also alleviated by neutralization of vascular cell adhesive molecule-1. Conclusions: These findings suggest that PolyI:C preferentially recruits and activates hepatic NK cells, which may be responsible for the mild hepatitis. (C) 2004 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
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页码:966 / 973
页数:8
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