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培养的人肝细胞中凝血因子 VIII 的合成。

Synthesis of factor VIII in human hepatocytes in culture.

作者信息

Ingerslev J, Christiansen B S, Heickendorff L, Munck Petersen C

机构信息

Department of Clinical Immunology, University Hospital Aarhus, Denmark.

出版信息

Thromb Haemost. 1988 Dec 22;60(3):387-91.

PMID:3149045
Abstract

Although several investigators have attempted to identify the site of synthesis of factor VIII (FVIII), the cellular species responsible for maintenance of plasma FVIII has not been clearly defined. Indications point at hepatocytes and certain endothelial cells. The present study investigated the FVIII coagulant antigen (VIII:Ag) of hepatocytes obtained by two-step collagenase digests of human liver pieces. Following Percoll gradient centrifugation, less than 1% of cells harvested were non-parenchymal. Lysates of freshly isolated and purified hepatocytes contained 165-250 mU of VIII:Ag/10(6) cells as defined by a two-site ELISA employing a haemophilic antibody against human FVIII. This material contained a single peak of VIII:Ag polypeptides as judged from the VIII:Ag ELISA profile of Mono-Q fast protein liquid chromatography fractions. A haemophilic antibody specific for epitopes of the light chain of FVIII, employed in immunoisolation of VIII:Ag in lysate of human hepatocytes, extracted a polypeptide pattern that was studied in a reduced SDS-PAGE electrophoresis gel and compared to that of immunoisolate from normal plasma. After electroblotting onto nitrocellulose and reaction with a monoclonal antibody towards the light chain of FVIII, the appearance of a doublet at 78-79 kDa in both these materials indicated the presence of the light chain of FVIII in human hepatocyte lysate. During culture, human hepatocytes secreted 20-80 mU of VIII:Ag per 1 x 10(6) cells per 24 hours. Further, a significant secretion of VIII:Ag was found in media of cultured human hepatoma cells, Hep-G2, whereas human blood monocytes and human fibroblasts did not secrete detectable VIII:Ag. In all of these cell cultures, vWf:Ag was indetectable or present as trace.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

尽管有几位研究人员试图确定凝血因子VIII(FVIII)的合成部位,但维持血浆FVIII水平的细胞类型尚未明确界定。有迹象表明是肝细胞和某些内皮细胞。本研究调查了通过两步胶原酶消化人肝组织获得的肝细胞中的FVIII凝血抗原(VIII:Ag)。在进行Percoll梯度离心后,收获的细胞中不到1%是非实质细胞。采用针对人FVIII的血友病抗体的双位点ELISA法测定,新鲜分离和纯化的肝细胞裂解物中每10⁶个细胞含有165 - 250 mU的VIII:Ag。从Mono - Q快速蛋白液相色谱馏分的VIII:Ag ELISA图谱判断,该物质含有VIII:Ag多肽的单峰。用人肝细胞裂解物中VIII:Ag免疫分离时使用的针对FVIII轻链表位的血友病抗体,提取了一种多肽模式,该模式在还原SDS - PAGE电泳凝胶中进行研究,并与正常血浆免疫分离物的模式进行比较。在电转印到硝酸纤维素膜上并与针对FVIII轻链的单克隆抗体反应后,这两种物质在78 - 79 kDa处均出现双峰,表明人肝细胞裂解物中存在FVIII轻链。在培养过程中,人肝细胞每24小时每1×10⁶个细胞分泌20 - 80 mU的VIII:Ag。此外,在培养的人肝癌细胞Hep - G2的培养基中发现有显著的VIII:Ag分泌,而人血单核细胞和成纤维细胞不分泌可检测到的VIII:Ag。在所有这些细胞培养物中,血管性血友病因子抗原(vWf:Ag)检测不到或仅为痕量。(摘要截短于250字)

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