F. Kuhnel et al., NF kappa B mediates apoptosis through transcriptional activation of Fas (CD95) in adenoviral hepatitis, J BIOL CHEM, 275(9), 2000, pp. 6421-6427
NF kappa B is an essential survival factor in several physiological conditi
ons such as embryonal liver development and liver regeneration. However, NF
kappa B is also a main mediator of the cellular response to a variety of e
xtracellular stress stimuli, and it has been shown that some viral-induced
host cell apoptosis appears to be dependent on NF kappa B activation, The a
ctivation of NF kappa B upon viral infection may be a rapid way of initiati
ng an innate immune response against the viral particles, We have assessed
the role of NFkB during the early phase of adenoviral hepatitis in a nude m
ouse model using an adenoviral vector expressing a mutant form of I kappa B
alpha. Administration of a LacZ-expressing adenoviral vector induces NFkB
DNA and correlates with the up-regulation of Fas (CD95) mRNA, but not Fast
(CD95L) mRNA, during the early phase of adenoviral hepatitis. The rapid inc
rease in NF kappa B DNA binding after adenoviral infection of the liver cou
ld be very effectively inhibited by I kappa B alpha. Compared with the LacZ
control virus, the I kappa B alpha-expressing adenoviral vector inhibits t
he increase of Fas (CD95) mRNA expression, in particular in the very early
phase of the hepatitis. Reporter gene experiments in hepatoma cell Lines wi
th a Fas promoter-luciferase construct indicated that the repression of Fas
(CD95) mRNA by I kappa B alpha was transcriptionally mediated. The functio
nal relevance of the NF kappa B-dependent increase in Fas (CD95) transcript
ion was assessed by caspase 3 assays and terminal dUTP nick-end labeling te
sts. Compared with the control, I kappa B alpha adenoviral infection result
ed in reduced caspase 3 activity during the early phase of viral hepatitis
and in a prevention of Liver cell apoptosis 24 h after adenoviral administr
ation. Therefore our study demonstrates a new pro-apoptotic function of NF
kappa B in Fas (CD95)-mediated apoptosis of hepatocytes. Interestingly, NF
kappa B mediates liver cell apoptosis upon viral infection even in a phase
where tumor necrosis factor-alpha is already induced, as shown by the time
curves of tumor necrosis factor-alpha serum levels, Therefore, the pro- or
anti-apoptotic role of NF kappa B appears to be more determined by the natu
re of the death stimulus than by the origin of the tissue.