TY - JOUR
T1 - STAT4 knockout mice are more susceptible to concanavalin A-induced T-cell hepatitis
AU - Wang, Yan
AU - Feng, Dechun
AU - Wang, Hua
AU - Xu, Ming Jiang
AU - Park, Ogyi
AU - Li, Yongmei
AU - Gao, Bin
N1 - Funding Information:
Supported by the intramural program of the NIH–National Institute on Alcohol Abuse and Alcoholism (B.G.), the China Scholarship Council (Y.W.), the Wu Mengchao Medical Science Foundation (Y.W.), and National Natural Science Foundation of China grant 81300312 (Y.W.). The Liver Tissue Cell Distribution System, University of Minnesota, Minneapolis, MN, is supported by NIH contract N01-DK-7-0004/HHSN267200700004C .
PY - 2014/6
Y1 - 2014/6
N2 - STAT4, which is activated mainly by IL-12, promotes inflammatory responses by inducing Th1 and Th2 cytokines. Recent genome-wide association studies indicate that STAT4 gene variants are associated with risk of various types of liver diseases, but how STAT4 contributes to liver disease pathogenesis remains obscure. In this study, STAT4 activation was detected in liver immune cells from patients with viral hepatitis and autoimmune hepatitis, as well as in a mouse model of concanavalin A (Con A)-induced hepatitis. Such STAT4 activation was detected mainly in T cells, natural killer T cells, and macrophages and Kupffer cells, and was diminished in Il12a-/- and Il12b-/- mice. As expected, disruption of the Stat4 gene reduced production of Th1 and Th2 cytokines, but surprisingly exacerbated Con A-induced liver injury. Similarly, disruption of Il12a or Il12b also augmented Con A-induced hepatocellular damage. Further studies showed that hepatic natural killer T (NKT) cells from Con A-treated Stat4-/- mice had higher levels of FasL expression and increased cytotoxicity against hepatocytes than those from Con A-treated WT mice. In vitro, blocking FasL attenuated Stat4-/- NKT cytotoxicity against hepatocytes. In conclusion, despite up-regulation of proinflammatory cytokines, STAT4 protects against acute T-cell hepatitis, which is mediated by direct or indirect down-regulation of FasL expression on NKT cells.
AB - STAT4, which is activated mainly by IL-12, promotes inflammatory responses by inducing Th1 and Th2 cytokines. Recent genome-wide association studies indicate that STAT4 gene variants are associated with risk of various types of liver diseases, but how STAT4 contributes to liver disease pathogenesis remains obscure. In this study, STAT4 activation was detected in liver immune cells from patients with viral hepatitis and autoimmune hepatitis, as well as in a mouse model of concanavalin A (Con A)-induced hepatitis. Such STAT4 activation was detected mainly in T cells, natural killer T cells, and macrophages and Kupffer cells, and was diminished in Il12a-/- and Il12b-/- mice. As expected, disruption of the Stat4 gene reduced production of Th1 and Th2 cytokines, but surprisingly exacerbated Con A-induced liver injury. Similarly, disruption of Il12a or Il12b also augmented Con A-induced hepatocellular damage. Further studies showed that hepatic natural killer T (NKT) cells from Con A-treated Stat4-/- mice had higher levels of FasL expression and increased cytotoxicity against hepatocytes than those from Con A-treated WT mice. In vitro, blocking FasL attenuated Stat4-/- NKT cytotoxicity against hepatocytes. In conclusion, despite up-regulation of proinflammatory cytokines, STAT4 protects against acute T-cell hepatitis, which is mediated by direct or indirect down-regulation of FasL expression on NKT cells.
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U2 - 10.1016/j.ajpath.2014.02.023
DO - 10.1016/j.ajpath.2014.02.023
M3 - Article
C2 - 24731448
AN - SCOPUS:84901033141
SN - 0002-9440
VL - 184
SP - 1785
EP - 1794
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 6
ER -