The oval cells of the liver have been identified as target cells of ch
emical carcinogens during rat hepatocarcinogenesis and are believed to
act as liver stem cells. In this study mice (strains C3H/EJ (C3H), C5
7/BL6J (C57) and hybrid B6C3F1 (F1)) were sacrified at 1, 3 and 7 days
after administration of a single dose of the carcinogen diethylnitros
amine (DEN), and histopathological studies of oval cells were evaluate
d using Haematoxylin and Eosin (H&E), Picro-Mallory (P-M), alpha-fetop
rotein (A-FP) and glutathione S-transferase placental form (GST-pi) st
aining techniques and electron microscopy (EM). Increased oval cell pr
oliferation was observed as soon as one day following exposure of the
mice to DEN, in a manner consistent with C3H and C57 mice exhibiting h
igh and low susceptibility to DEN respectively, with hybrid F1 mice be
ing intermediate in DEN sensitivity. This analysis indicates that, in
mice, oval cells are target cells at very early stages of liver carcin
ogenesis and supports the notion that oval cells are potential liver s
tem cells.