Cell Engineering Research Center and Department of Cell Biology, Fourth Military Medical University, Xi'an, China.
J Hepatol. 2012 Dec;57(6):1283-91. doi: 10.1016/j.jhep.2012.07.042. Epub 2012 Aug 7.
BACKGROUND & AIMS: Activated hepatic stellate cells (HSCs) located in the Disse's space play a crucial role in liver fibrosis. HAb18G/CD147, a tumor-related glycoprotein, is highly expressed in hepatocellular carcinoma cells and fibroblasts. Whether HAb18G/CD147 plays an important role in the hepatic fibrogenesis is unknown.
Immunohistochemistry for HAb18G/CD147 and α-smooth muscle actin expression in diseased liver tissues was used for correlation analysis. The function of HAb18G/CD147 in fibrogenesis was evaluated with the human HSCs LX-2 cell line and carbon tetrachloride-induced mouse liver fibrosis model. The specific antibody HAb18 targeting HAb18G/CD147 was injected intravenously into the mouse to investigate whether HAb18G/CD147 could be a potential target for liver fibrosis treatment.
HAb18G/CD147 is highly expressed on activated HSCs in the sinusoid. The positive rates of HAb18G/CD147 expression in human HBV-related liver cirrhosis, liver biopsy with HBV and liver adjacent to hemangioma were 95.6% (65/68), 14.8% (8/54) and 6.4% (8/125), respectively. HAb18G/CD147 expression was significantly correlated with the Child-Pugh grade (r=0.2848, p=0.0186) and with the expression of α-smooth muscle actin in HSCs (r=0.4434, p=0.0002) in liver cirrhosis. Transforming growth factor-β1 upregulated HAb18G/CD147 expression in LX-2 cells. Transfection of HAb18G/CD147 promoted the profibrogenic genes expression. In mouse liver fibrosis model, HAb18G/CD147 expression increased with the development of fibrogenesis and decreased during the liver fibrosis spontaneous recovery. The HAb18 targeting HAb18G/CD147 could attenuate liver fibrosis.
These data suggest that HAb18G/CD147 plays a role in HSC activation and is a potential therapeutic target in fibrosis/cirrhosis.
位于 Disse 间隙的活化的肝星状细胞(HSCs)在肝纤维化中起着关键作用。HAb18G/CD147 是一种与肿瘤相关的糖蛋白,在肝癌细胞和成纤维细胞中高表达。HAb18G/CD147 是否在肝纤维化发生中起重要作用尚不清楚。
采用免疫组化法检测病变肝组织中 HAb18G/CD147 和α-平滑肌肌动蛋白的表达,并进行相关性分析。用人 HSCs LX-2 细胞系和四氯化碳诱导的小鼠肝纤维化模型评估 HAb18G/CD147 在纤维化中的作用。通过静脉注射针对 HAb18G/CD147 的特异性抗体 HAb18 来研究 HAb18G/CD147 是否可以成为治疗肝纤维化的潜在靶点。
HAb18G/CD147 在窦状隙活化的 HSCs 上高表达。人 HBV 相关肝硬化、HBV 肝活检和肝血管瘤旁肝组织中 HAb18G/CD147 表达的阳性率分别为 95.6%(65/68)、14.8%(8/54)和 6.4%(8/125)。HAb18G/CD147 的表达与 Child-Pugh 分级(r=0.2848,p=0.0186)和肝硬化中 HSCs 的α-平滑肌肌动蛋白表达呈显著相关(r=0.4434,p=0.0002)。转化生长因子-β1 上调 LX-2 细胞中 HAb18G/CD147 的表达。HAb18G/CD147 的转染促进了致纤维生成基因的表达。在小鼠肝纤维化模型中,HAb18G/CD147 的表达随着纤维化的发展而增加,在肝纤维化自发恢复过程中减少。针对 HAb18G/CD147 的 HAb18 可减轻肝纤维化。
这些数据表明,HAb18G/CD147 在 HSC 活化中起作用,是纤维化/肝硬化的潜在治疗靶点。