Effects and regulation of osteopontin in rat hepatic stellate cells |
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Authors: | Lee Sung Hee Seo Geom Seog Park Young Nyun Yoo Tae Moo Sohn Dong Hwan |
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Affiliation: | Medicinal Resources Research Center, College of Pharmacy, Wonkwang University, Iksan, Jeonbuk 570-749, Republic of Korea. |
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Abstract: | Using a cDNA microarray, we identified osteopontin (OPN) as one of the genes upregulated in cultured activated hepatic stellate cells (HSCs). Northern and western blot analyses showed that OPN was increasingly expressed during the progressive activation of cultured rat HSCs, and a significant increase in OPN was observed in carbon tetrachloride-induced rat liver fibrosis. In biliary atresia, OPN protein was predominantly expressed in Kupffer cells and HSCs in the necrotic areas. Incubation of HSCs with recombinant OPN-induced significant proliferative and migratory effects, and induced matrix metalloproteinase 2 production and activation. Moreover, OPN increased type I collagen production and type II transforming growth factor-beta receptor mRNA and protein. In conclusion, this study shows that OPN is expressed in activated HSCs and suggests that the upregulation of OPN might be a central pathway of HSC activation. |
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Keywords: | ECM, extracellular matrix MMP-2, matrix metalloproteinase 2 MTI-MMP, membrane type I matrix metalloproteinase OPN, osteopontin PDGF, platelet-derived growth factor TGF-β, transforming growth factor β TβRII, type II TGF-β, receptor TIMP-2 t, issue inhibitor of metalloproteinase 2 |
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