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Short Communications |
From the Departments of Anatomy*
and Internal
Medicine,
Osaka City University Medical
School, Osaka, and the Department of Anatomy,
Fukui Medical University, Fukui, Japan
Suppression subtractive hybridization was used to clone genes
associated with the activation of hepatic stellate cells and 13 genes
were found to be dominantly expressed in activated stellate cells.
Among them, one was identical to the 421-837th base pairs of
cDNA sequence reported for rat prion-related protein (PrP). In cultured
stellate cells, PrP mRNA expression increased in a
time-dependent manner in parallel with smooth muscle (SM)
-actin
mRNA expression. In situ hybridization demonstrated that
PrP mRNA was localized in and around the fibrous septa of carbon
tetrachloride (CCl4)-treated liver. Cellular PrP
(PrPc) was produced by culture-activated stellate
cells, and immunohistochemically detected in the fibrous septa
of CCl4-damaged liver and sinusoidal linings of common bile
duct-ligated liver, consistent with the localization of SM
-actin. Immunoelectron microscopy revealed that PrPc
resided on the plasma membrane of stellate cells. These results
indicate that PrP expression is closely related to stellate cell
activation associated with fibrogenic stimuli.
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