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正常人肝脏胆管上皮细胞的免疫隔离与培养

Immuno-isolation and culture of biliary epithelial cells from normal human liver.

作者信息

Joplin R, Strain A J, Neuberger J M

机构信息

Department of Medicine, University of Birmingham, Queen Elizabeth Hospital, United Kingdom.

出版信息

In Vitro Cell Dev Biol. 1989 Dec;25(12):1189-92. doi: 10.1007/BF02621273.

Abstract

Biliary epithelial cells (BEC) lining the intra-hepatic biliary ducts are the site of damage in several immunologically mediated liver diseases. BEC are difficult to isolate since they represent only 5% of the total cell number in normal liver. In this communication, a novel method for their isolation from normal liver is presented using a monoclonal antibody (HEA125) with specificity for an epithelial cell surface glyco-protein reported to be expressed in liver only by biliary epithelium. By combining differential density centrifugation and immuno-magnetic separation using HEA125 pure BEC (10(5) cells/g fresh tissue) were prepared routinely. These cells were maintained in culture for up to 4 weeks with significant increases in cell numbers. The ability to prepare BEC from human liver offers an opportunity to develop In Vitro models to investigate the aetiology of diseases of intra-hepatic biliary epithelium.

摘要

肝内胆管内衬的胆管上皮细胞(BEC)是几种免疫介导性肝病的损伤部位。BEC很难分离,因为它们在正常肝脏中仅占细胞总数的5%。在本通讯中,提出了一种从正常肝脏中分离BEC的新方法,该方法使用了一种单克隆抗体(HEA125),该抗体对一种上皮细胞表面糖蛋白具有特异性,据报道该糖蛋白仅在胆管上皮中表达于肝脏。通过结合密度梯度离心和使用HEA125的免疫磁珠分离,常规制备了纯化的BEC(10⁵个细胞/克新鲜组织)。这些细胞在培养中可维持长达4周,细胞数量显著增加。从人肝脏中制备BEC的能力为开发体外模型以研究肝内胆管上皮疾病的病因提供了机会。

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