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嘌呤霉素氨基核苷诱导的肾小球硬化症细胞外基质的时间进程研究

Time course study of the extracellular matrix in puromycin-aminonucleoside-induced glomerulosclerosis.

作者信息

Kanaya H, Ishitobi F, Ono Y, Yaguchi T, Ueda Y

机构信息

Second Department of Pathology, Dokkyo University School of Medicine, Tochigi, Japan.

出版信息

Nihon Jinzo Gakkai Shi. 1994 Apr;36(4):307-16.

PMID:8022102
Abstract

The purpose of this study was to investigate the mechanism of glomerulosclerosis, which is an important histopathological feature of various renal diseases. Puromycin aminonucleoside (PAN) was administered to rats to produce glomerular lesions, and the kidneys were examined by repeated renal biopsy with light microscopy and immunohistochemical detection of glomerular extracellular matrix (ECM) components (laminin, fibronectin, type I, III, and IV collagen). Immunohistochemical studies utilizing the streptavidin-biotin method showed marked accumulation of laminin and type IV collagen in the adhesions between the glomerular epithelium and Bowman's capsule, as well as in the mesangial matrix. Fibronectin was detected in the normal mesangium and the basement membrane of Bowman's capsule, while adhesions and the matrix accumulations were also positive. The sclerotic lesions of the glomeruli were also stained for type I and III collagen, which exist in normal interstitial tissue, but never in healthy glomeruli. Type I collagen appeared in the lesions after type III collagen. All of the ECM components examined in this study were present in advanced glomerulosclerosis and showed distinctive patterns of progression. These finding suggest that abnormal accumulation and production of ECM components in the glomeruli may have a role in the development of glomerulosclerosis.

摘要

本研究的目的是探究肾小球硬化的机制,肾小球硬化是各种肾脏疾病的重要组织病理学特征。给大鼠注射嘌呤霉素氨基核苷(PAN)以产生肾小球病变,并通过重复肾活检,利用光学显微镜和免疫组织化学方法检测肾小球细胞外基质(ECM)成分(层粘连蛋白、纤连蛋白、I型、III型和IV型胶原)来检查肾脏。利用链霉亲和素-生物素方法进行的免疫组织化学研究显示,层粘连蛋白和IV型胶原在肾小球上皮与鲍曼囊之间的粘连处以及系膜基质中显著积聚。纤连蛋白在正常系膜和鲍曼囊基底膜中被检测到,粘连处和基质积聚处也呈阳性。肾小球的硬化病变也用I型和III型胶原染色,这两种胶原存在于正常间质组织中,但在健康肾小球中从未出现。I型胶原在III型胶原之后出现在病变中。本研究中检测的所有ECM成分都存在于晚期肾小球硬化中,并呈现出独特的进展模式。这些发现表明,肾小球中ECM成分的异常积聚和产生可能在肾小球硬化的发展中起作用。

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