Lee Sung Hee, Seo Geom Seog, Park Young Nyun, Yoo Tae Moo, Sohn Dong Hwan
Medicinal Resources Research Center, College of Pharmacy, Wonkwang University, Iksan, Jeonbuk 570-749, Republic of Korea.
Biochem Pharmacol. 2004 Dec 15;68(12):2367-78. doi: 10.1016/j.bcp.2004.08.022.
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.
利用cDNA微阵列,我们鉴定出骨桥蛋白(OPN)是培养的活化肝星状细胞(HSC)中上调的基因之一。Northern印迹和Western印迹分析表明,在培养的大鼠HSC逐渐活化过程中OPN表达增加,并且在四氯化碳诱导的大鼠肝纤维化中观察到OPN显著增加。在胆道闭锁中,OPN蛋白主要在坏死区域的库普弗细胞和HSC中表达。用重组OPN孵育HSC可诱导显著的增殖和迁移作用,并诱导基质金属蛋白酶2的产生和激活。此外,OPN增加I型胶原蛋白的产生以及II型转化生长因子-β受体的mRNA和蛋白表达。总之,本研究表明OPN在活化的HSC中表达,并提示OPN的上调可能是HSC活化的核心途径。