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肝脏纤维化中的前胶原C蛋白酶增强子1(PCPE-1)

Procollagen C-Proteinase Enhancer 1 (PCPE-1) in Liver Fibrosis.

作者信息

Kessler Efrat, Hassoun Eyal

机构信息

Maurice and Gabriela Goldschleger Eye Research Institute, Tel Aviv University Sackler Faculty of Medicine, Sheba Medical Center, Tel-Hashomer, Israel.

Clinical Biochemistry and Pharmacology Institute, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel.

出版信息

Methods Mol Biol. 2019;1944:189-201. doi: 10.1007/978-1-4939-9095-5_14.

Abstract

Fibrosis is characterized by excessive deposition of collagen and additional extracellular matrix (ECM) components in response to chronic injuries. Liver fibrosis often results from chronic hepatitis C virus infection and alcohol abuse that can deteriorate to cirrhosis and liver failure. Current noninvasive diagnostic methods of liver fibrosis are limited in their ability to detect and differentiate between early and intermediate stages of fibrosis. New biomarkers of fibrosis that reflect ECM turnover are therefore badly needed. Procollagen C-proteinase enhancer 1 (PCPE-1), a connective tissue glycoprotein that functions as a positive regulator of C-terminal procollagen processing and subsequent collagen fibril assembly, is a promising candidate. Its tissue distribution and expression profile overlap those of collagen, and its expression in fibrosis is upregulated in parallel to the increase in collagen expression. The potential of PCPE-1 as a biomarker of liver fibrosis was recently established using a CCl mouse model of liver fibrosis by showing that the increase in collagen and PCPE-1 content in the fibrotic mouse liver was reflected by elevated plasma levels of PCPE-1. This was achieved using a newly developed highly sensitive, specific, accurate, and reproducible ELISA for mouse PCPE-1, which is based on commercially available antibodies and is offered as a new research tool in the field. A similar ELISA test was developed for human PCPE-1, and preliminary results with plasma from liver fibrosis patients revealed increased plasma concentrations of PCPE-1 in some patients. The protocols of both ELISA tests are outlined herein in great detail to permit their application by any laboratory with similar interests.

摘要

纤维化的特征是在慢性损伤的反应中,胶原蛋白和其他细胞外基质(ECM)成分过度沉积。肝纤维化通常由慢性丙型肝炎病毒感染和酒精滥用引起,可恶化为肝硬化和肝衰竭。目前肝纤维化的非侵入性诊断方法在检测和区分纤维化早期和中期的能力方面存在局限性。因此,迫切需要反映ECM周转的新的纤维化生物标志物。前胶原C蛋白酶增强子1(PCPE-1)是一种结缔组织糖蛋白,作为C端前胶原加工及随后胶原纤维组装的正向调节因子,是一个很有前景的候选物。它的组织分布和表达谱与胶原蛋白的重叠,并且其在纤维化中的表达与胶原蛋白表达的增加平行上调。最近,通过使用肝纤维化的CCl小鼠模型,证明纤维化小鼠肝脏中胶原蛋白和PCPE-1含量的增加反映在血浆PCPE-1水平的升高上,从而确立了PCPE-1作为肝纤维化生物标志物的潜力。这是通过使用一种新开发的针对小鼠PCPE-1的高度灵敏、特异、准确且可重复的ELISA实现的,该ELISA基于市售抗体,作为该领域的一种新研究工具提供。针对人PCPE-1也开发了类似的ELISA检测方法,对肝纤维化患者血浆的初步结果显示,一些患者的血浆PCPE-1浓度升高。本文详细概述了两种ELISA检测方法的方案,以便任何有类似兴趣的实验室都能应用。

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