To clone genes associated with the activation of hepatic stellate cells, su
ppression subtractive hybridization was employed and thirteen genes were fo
und to be dominantly expressed in activated stellate cells. Among them, one
was 100% identical to the 421-837th base pairs of cDNA sequence reported f
or rat prion-related protein (PrP). Northern blot analysis demonstrated tha
t PrP mRNA expression increased in cultured stellate cells in a time-depend
ent manner, while it was hardly detected in freshly isolated ones. As demon
strated by in situ hybridization, PrP mRNA was localized in and around the
fibrous septa of carbon tetrachloride (CCl4)-treated liver. Western blot an
alysis confirmed the expression of PrP in cultured stellate cells and furth
er demonstrated that expression of PrP as well as that of smooth muscle alp
ha-actin increased in cultured stellate cells in a rime-dependent manner. M
oreover, PrP was detected immunohistochemically in the fibrous septa of CCl
4-damaged liver and sinusoidal linings of common bile duct-ligated liver. T
hese results indicate that PrP gene and protein are dominantly expressed in
activated stellate cells.