Yovchev Mladen I, Grozdanov Petar N, Joseph Brigid, Gupta Sanjeev, Dabeva Mariana D
Marion Bessin Liver Research Center, Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA.
Hepatology. 2007 Jan;45(1):139-49. doi: 10.1002/hep.21448.
Hepatic progenitor/oval cells appear in injured livers when hepatocyte proliferation is impaired. These cells can differentiate into hepatocytes and cholangiocytes and could be useful for cell and gene therapy applications. In this work, we studied progenitor/oval cell surface markers in the liver of rats subjected to 2-acetylaminofluorene treatment followed by partial hepatectomy (2-AAF/PH) by using rat genome 230 2.0 Array chips and subsequent RT-PCR, immunofluorescent (IF), immunohistochemical (IHC) and in situ hybridization (ISH) analyses. We also studied expression of the identified novel cell surface markers in fetal rat liver progenitor cells and FAO-1 hepatoma cells. Novel cell surface markers in adult progenitor cells included tight junction proteins, integrins, cadherins, cell adhesion molecules, receptors, membrane channels and other transmembrane proteins. From the panel of 21 cell surface markers, 9 were overexpressed in fetal progenitor cells, 6 in FAO-1 cells and 6 are unique for the adult progenitors (CD133, claudin-7, cadherin 22, mucin-1, ros-1, Gabrp). The specificity of progenitor/oval cell surface markers was confirmed by ISH and double IF analyses. Moreover, study of progenitor cells purified with Ep-CAM antibodies from D-galactosamine injured rat liver, a noncarcinogenic model of progenitor cell activation, verified that progenitor cells expressed these markers.
We identified novel cell surface markers specific for hepatic progenitor/oval cells, which offers powerful tool for their identification, isolation and studies of their physiology and pathophysiology. Our studies also reveal the mesenchymal/epithelial phenotype of these cells and the existence of species diversity in the hepatic progenitor cell identity.
当肝细胞增殖受损时,肝祖细胞/卵圆细胞出现在受损肝脏中。这些细胞可分化为肝细胞和胆管细胞,可能对细胞和基因治疗应用有用。在本研究中,我们通过使用大鼠基因组230 2.0阵列芯片以及随后的逆转录聚合酶链反应(RT-PCR)、免疫荧光(IF)、免疫组织化学(IHC)和原位杂交(ISH)分析,研究了经2-乙酰氨基芴处理后行部分肝切除术(2-AAF/PH)的大鼠肝脏中祖细胞/卵圆细胞的表面标志物。我们还研究了所鉴定的新型细胞表面标志物在胎鼠肝祖细胞和FAO-1肝癌细胞中的表达。成年祖细胞中的新型细胞表面标志物包括紧密连接蛋白、整合素、钙黏蛋白、细胞黏附分子、受体、膜通道和其他跨膜蛋白。在21种细胞表面标志物中,9种在胎鼠祖细胞中过表达,6种在FAO-1细胞中过表达,6种是成年祖细胞所特有的(CD133、claudin-7、钙黏蛋白22、黏蛋白-1、ros-1、GABrp)。通过ISH和双重IF分析证实了祖细胞/卵圆细胞表面标志物的特异性。此外,在用Ep-CAM抗体从D-半乳糖胺损伤的大鼠肝脏(一种祖细胞激活的非致癌模型)中纯化的祖细胞的研究中,证实了祖细胞表达这些标志物。
我们鉴定了肝祖细胞/卵圆细胞特有的新型细胞表面标志物,这为其鉴定、分离以及生理和病理生理学研究提供了有力工具。我们的研究还揭示了这些细胞的间充质/上皮表型以及肝祖细胞身份存在物种多样性。