Time course study of the extracellular matrix in puromycin aminonucleoside-induced glomerulosclerosis
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...
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Veröffentlicht in: | Nihon Jinzo Gakkai shi 1994, Vol.36(4), pp.307-316 |
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description | 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. Fbbronectin 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. |
doi_str_mv | 10.14842/jpnjnephrol1959.36.307 |
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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. Fbbronectin 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.</description><identifier>ISSN: 0385-2385</identifier><identifier>EISSN: 1884-0728</identifier><identifier>DOI: 10.14842/jpnjnephrol1959.36.307</identifier><identifier>PMID: 8022102</identifier><language>eng</language><publisher>Japan: Japanese Society of Nephrology</publisher><subject>Animals ; Extracellular Matrix Proteins - metabolism ; Extracellular matrix, glomerulosclerosis, PAN nephrosis, immunohistochemistry ; Glomerulosclerosis, Focal Segmental - chemically induced ; Glomerulosclerosis, Focal Segmental - metabolism ; Glomerulosclerosis, Focal Segmental - pathology ; Immunohistochemistry ; Kidney Glomerulus - metabolism ; Kidney Glomerulus - pathology ; Male ; Puromycin Aminonucleoside ; Rats ; Rats, Sprague-Dawley</subject><ispartof>The Japanese Journal of Nephrology, 1994, Vol.36(4), pp.307-316</ispartof><rights>Japanese Society of Nephrology</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8022102$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>KANAYA, HIROAKI</creatorcontrib><creatorcontrib>ISHITOBI, FUMIO</creatorcontrib><creatorcontrib>ONO, YUKO</creatorcontrib><creatorcontrib>YAGUCHI, TADASHI</creatorcontrib><creatorcontrib>VEDA, YOSHIHIKO</creatorcontrib><title>Time course study of the extracellular matrix in puromycin aminonucleoside-induced glomerulosclerosis</title><title>Nihon Jinzo Gakkai shi</title><addtitle>Jpn J Nephrol</addtitle><description>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. Fbbronectin 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.</description><subject>Animals</subject><subject>Extracellular Matrix Proteins - metabolism</subject><subject>Extracellular matrix, glomerulosclerosis, PAN nephrosis, immunohistochemistry</subject><subject>Glomerulosclerosis, Focal Segmental - chemically induced</subject><subject>Glomerulosclerosis, Focal Segmental - metabolism</subject><subject>Glomerulosclerosis, Focal Segmental - pathology</subject><subject>Immunohistochemistry</subject><subject>Kidney Glomerulus - metabolism</subject><subject>Kidney Glomerulus - pathology</subject><subject>Male</subject><subject>Puromycin Aminonucleoside</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><issn>0385-2385</issn><issn>1884-0728</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1994</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkNtqwzAMhs3Y6ErXRxjzC6TzKU5yOcpOrLCb7jq4ttI6OHGwE2jffh4tvZgufgl94kcSQk-UrKgoBXtuh77tYTgE72iVVysuV5wUN2hOy1JkpGDlLZoTXuYZS3KPljG2JIWspOB0hmYlYYwSNkewtR1g7acQAcdxMifsGzweAMNxDEqDc5NTAXdqDPaIbY-HKfjupFOlOtv7ftIOfLQGMtubSYPBe-c7CJPzMaGQWHxAd41yEZaXvEA_b6_b9Ue2-X7_XL9sspZTNmYVKbXId4I0TBY5hx3lijDNgDcyp6n9p6LYgaINN1IrYypDlJRFSTStKF-gx7PvMO06MPUQbKfCqb6cm_jXmbdxVHu4chVGm3at__215rIWFyHFdUofVKih57-iAXk6</recordid><startdate>1994</startdate><enddate>1994</enddate><creator>KANAYA, HIROAKI</creator><creator>ISHITOBI, FUMIO</creator><creator>ONO, YUKO</creator><creator>YAGUCHI, TADASHI</creator><creator>VEDA, YOSHIHIKO</creator><general>Japanese Society of Nephrology</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope></search><sort><creationdate>1994</creationdate><title>Time course study of the extracellular matrix in puromycin aminonucleoside-induced glomerulosclerosis</title><author>KANAYA, HIROAKI ; ISHITOBI, FUMIO ; ONO, YUKO ; YAGUCHI, TADASHI ; VEDA, YOSHIHIKO</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-j312t-908c45b40f26753eb13a02c2e3f65140f651447bea1f3d6cadd9d0a66780c1913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1994</creationdate><topic>Animals</topic><topic>Extracellular Matrix Proteins - metabolism</topic><topic>Extracellular matrix, glomerulosclerosis, PAN nephrosis, immunohistochemistry</topic><topic>Glomerulosclerosis, Focal Segmental - chemically induced</topic><topic>Glomerulosclerosis, Focal Segmental - metabolism</topic><topic>Glomerulosclerosis, Focal Segmental - pathology</topic><topic>Immunohistochemistry</topic><topic>Kidney Glomerulus - metabolism</topic><topic>Kidney Glomerulus - pathology</topic><topic>Male</topic><topic>Puromycin Aminonucleoside</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><toplevel>online_resources</toplevel><creatorcontrib>KANAYA, HIROAKI</creatorcontrib><creatorcontrib>ISHITOBI, FUMIO</creatorcontrib><creatorcontrib>ONO, YUKO</creatorcontrib><creatorcontrib>YAGUCHI, TADASHI</creatorcontrib><creatorcontrib>VEDA, YOSHIHIKO</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><jtitle>Nihon Jinzo Gakkai shi</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>KANAYA, HIROAKI</au><au>ISHITOBI, FUMIO</au><au>ONO, YUKO</au><au>YAGUCHI, TADASHI</au><au>VEDA, YOSHIHIKO</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Time course study of the extracellular matrix in puromycin aminonucleoside-induced glomerulosclerosis</atitle><jtitle>Nihon Jinzo Gakkai shi</jtitle><addtitle>Jpn J Nephrol</addtitle><date>1994</date><risdate>1994</risdate><volume>36</volume><issue>4</issue><spage>307</spage><epage>316</epage><pages>307-316</pages><issn>0385-2385</issn><eissn>1884-0728</eissn><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. Fbbronectin 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.</abstract><cop>Japan</cop><pub>Japanese Society of Nephrology</pub><pmid>8022102</pmid><doi>10.14842/jpnjnephrol1959.36.307</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Extracellular Matrix Proteins - metabolism Extracellular matrix, glomerulosclerosis, PAN nephrosis, immunohistochemistry Glomerulosclerosis, Focal Segmental - chemically induced Glomerulosclerosis, Focal Segmental - metabolism Glomerulosclerosis, Focal Segmental - pathology Immunohistochemistry Kidney Glomerulus - metabolism Kidney Glomerulus - pathology Male Puromycin Aminonucleoside Rats Rats, Sprague-Dawley |
title | Time course study of the extracellular matrix in puromycin aminonucleoside-induced glomerulosclerosis |
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