While the fas/fas ligand system has been extensively investigated in immuno
-competent cells, the place of this system in the physiology and pathophysi
ology of liver cells remains to be clarified. Although we know that fas is
present at the surface of hepatocytes - the main hepatic cells - the role o
f this membranous protein in physiological conditions is not yet elucidated
. However it is the localization of fas on the plasma membrane of hepatocyt
es which explains why these cells are mainly destroyed by apoptosis - in a
picture resembling human fulminant hepatitis - when mice are administered w
ith anti-fas antibodies or fas ligand. It is also established that fas is s
urexpressed in some human chronic liver diseases, such as those induced by
hepatitis B or C virus, a situation which could explain the pathogenesis of
some liver lesions occurring during these diseases, such as the apoptosis
of hepatocytes in piecemeal necrosis. Finally the fact that caspases, a gro
up of cysteine proteases activated in fas-induced apoptosis, opens the way
to inhibition of these enzymes by synthetic peptides and to prevent and tre
at hepatocyte apoptosis. Demonstration of this possibility has been recentl
y reported in animals presenting fulminant hepatitis induced by anti-fas an
tibodies. (C) 1998 Elsevier, Paris.