TY - JOUR
T1 - NF-κB is activated in cholestasis and functions to reduce liver injury
AU - Miyoshi, Hideyuki
AU - Rust, Christian
AU - Guicciardi, M. Eugenia
AU - Gores, Gregory J.
PY - 2001
Y1 - 2001
N2 - Selected bile acids activate a nuclear factor-kappa B (NF-κB)-dependent survival signaling cascade in cultured hepatocytes. These data suggest that in cholestasis where liver tissue bile acid concentrations are increased, NF-κB should be activated and inhibition of NF-κB should potentiate liver injury. Our aims were to test these two predictions. Cholestasis was obtained by common bile duct ligation in mice. NF-κB activation was demonstrated in nuclear extracts by the electrophoretic mobility gel shift assay from 3-day bile duct-ligated (BDL) mice but not in controls. Immunohistochemistry for NF-κB demonstrated nuclear localization in hepatocytes of BDL mice consistent with its activation in this liver cell type. Electrophoretic mobility gel shift assay and immunohistochemistry for NF-κB in BDL tumor necrosis factor-receptor I knockout mice demonstrated hepatocyte NF-κB activation, suggesting that tumor necrosis factor-α was not responsible for the activation of this transcription factor. Liver injury was assessed in BDL mice after administration of the adenovirus 5 inhibitor of kappa B superrepressor (Ad5IκBsr) to inhibit NF-κB. TUNEL-positive cells and serum alanine aminotransferase values were increased at least threefold in mice treated with the Ad5IκBsr versus the empty virus. Liver histology also demonstrated increased liver injury in the BDL mice treated with the Ad5IκBsr. In conclusion, NF-κB is activated in hepatocytes during obstructive cholestasis and functions to reduce liver injury.
AB - Selected bile acids activate a nuclear factor-kappa B (NF-κB)-dependent survival signaling cascade in cultured hepatocytes. These data suggest that in cholestasis where liver tissue bile acid concentrations are increased, NF-κB should be activated and inhibition of NF-κB should potentiate liver injury. Our aims were to test these two predictions. Cholestasis was obtained by common bile duct ligation in mice. NF-κB activation was demonstrated in nuclear extracts by the electrophoretic mobility gel shift assay from 3-day bile duct-ligated (BDL) mice but not in controls. Immunohistochemistry for NF-κB demonstrated nuclear localization in hepatocytes of BDL mice consistent with its activation in this liver cell type. Electrophoretic mobility gel shift assay and immunohistochemistry for NF-κB in BDL tumor necrosis factor-receptor I knockout mice demonstrated hepatocyte NF-κB activation, suggesting that tumor necrosis factor-α was not responsible for the activation of this transcription factor. Liver injury was assessed in BDL mice after administration of the adenovirus 5 inhibitor of kappa B superrepressor (Ad5IκBsr) to inhibit NF-κB. TUNEL-positive cells and serum alanine aminotransferase values were increased at least threefold in mice treated with the Ad5IκBsr versus the empty virus. Liver histology also demonstrated increased liver injury in the BDL mice treated with the Ad5IκBsr. In conclusion, NF-κB is activated in hepatocytes during obstructive cholestasis and functions to reduce liver injury.
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U2 - 10.1016/S0002-9440(10)64043-6
DO - 10.1016/S0002-9440(10)64043-6
M3 - Article
C2 - 11238044
AN - SCOPUS:0034745492
SN - 0002-9440
VL - 158
SP - 967
EP - 975
JO - American Journal of Pathology
JF - American Journal of Pathology
IS - 3
ER -