Degradation of type IV collagen during the development of fetal rat lung

Lung structure undergoes rapid remodeling during late gestation as a functional respiratory unit is formed. To determine the role of collagen turnover in this process, particularly the basement membrane component, we studied the degradation of collagen in a series of fetal rats from day 18 of gestat...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:American journal of respiratory cell and molecular biology 1993-07, Vol.9 (1), p.99-105
Hauptverfasser: ARDEN, M. G, SPEARMAN, M. A, ADAMSON, I. Y. R
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 105
container_issue 1
container_start_page 99
container_title American journal of respiratory cell and molecular biology
container_volume 9
creator ARDEN, M. G
SPEARMAN, M. A
ADAMSON, I. Y. R
description Lung structure undergoes rapid remodeling during late gestation as a functional respiratory unit is formed. To determine the role of collagen turnover in this process, particularly the basement membrane component, we studied the degradation of collagen in a series of fetal rats from day 18 of gestation to full term. During the period of rapid cell proliferation to day 20, the collagen level per milligram of lung did not change though the rate of synthesis increased. More than 40% of new collagen was rapidly degraded. At the end of the growth phase, collagen synthesis rose rapidly as the total collagen content increased in the lung. Over this period, little Type I collagenase activity could be detected, but degradation of Type IV collagen was readily measured and was maximal at 18 to 20 days. The enzyme(s) was almost all present in the active form, and evidence for dissolution of the subepithelial basement membrane was also found by electron microscopy. Using isolated fetal epithelial cells and fibroblasts, supernatants of both cell types showed degradative activity for Type IV collagen, particularly at days 18 to 20. The major enzyme involved appears to be a 72 kD collagenase, as shown by zymography and by mRNA expression in both cell types. The results demonstrate that rapid degradation of Type IV collagen occurs during the growth phase of late fetal lung development, and that both epithelial and stromal cells contribute to collagenolytic activity.
doi_str_mv 10.1165/ajrcmb/9.1.99
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_75856482</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>75856482</sourcerecordid><originalsourceid>FETCH-LOGICAL-c317t-2d3817aca8f592b3f28086ad71bd7783f6bcea5f4371268ecbb7e3579a7327373</originalsourceid><addsrcrecordid>eNo9kM1LwzAYxoMoc06PHoUcxFu3pmma5CjzY4OBF_Ua0vRN7eiXSSrsv7djZaf3gefHw8sPoXsSLwnJ2ErvnWnylVySpZQXaE4YZVEqhbwcc5ymEWGpvEY33u_jmCSCkBmaCUpFJuI52rxA6XShQ9W1uLM4HHrA229surrWJbS4GFzVljj8AC7gD-qub6ANR9RC0DV2OuB6aMtbdGV17eFuugv09fb6ud5Eu4_37fp5FxlKeIiSggrCtdHCMpnk1CYiFpkuOMkLzgW1WW5AM5tSTpJMgMlzDpRxqTlNOOV0gZ5Ou73rfgfwQTWVNzB-20I3eMWZYFkqkhGMTqBxnfcOrOpd1Wh3UCRWR3PqZE5JRZSUI_8wDQ95A8WZnlSN_ePUa290bZ1uTeXPGOU8Thij_zm1duI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>75856482</pqid></control><display><type>article</type><title>Degradation of type IV collagen during the development of fetal rat lung</title><source>MEDLINE</source><source>Journals@Ovid Complete</source><creator>ARDEN, M. G ; SPEARMAN, M. A ; ADAMSON, I. Y. R</creator><creatorcontrib>ARDEN, M. G ; SPEARMAN, M. A ; ADAMSON, I. Y. R</creatorcontrib><description>Lung structure undergoes rapid remodeling during late gestation as a functional respiratory unit is formed. To determine the role of collagen turnover in this process, particularly the basement membrane component, we studied the degradation of collagen in a series of fetal rats from day 18 of gestation to full term. During the period of rapid cell proliferation to day 20, the collagen level per milligram of lung did not change though the rate of synthesis increased. More than 40% of new collagen was rapidly degraded. At the end of the growth phase, collagen synthesis rose rapidly as the total collagen content increased in the lung. Over this period, little Type I collagenase activity could be detected, but degradation of Type IV collagen was readily measured and was maximal at 18 to 20 days. The enzyme(s) was almost all present in the active form, and evidence for dissolution of the subepithelial basement membrane was also found by electron microscopy. Using isolated fetal epithelial cells and fibroblasts, supernatants of both cell types showed degradative activity for Type IV collagen, particularly at days 18 to 20. The major enzyme involved appears to be a 72 kD collagenase, as shown by zymography and by mRNA expression in both cell types. The results demonstrate that rapid degradation of Type IV collagen occurs during the growth phase of late fetal lung development, and that both epithelial and stromal cells contribute to collagenolytic activity.</description><identifier>ISSN: 1044-1549</identifier><identifier>EISSN: 1535-4989</identifier><identifier>DOI: 10.1165/ajrcmb/9.1.99</identifier><identifier>PMID: 8338680</identifier><identifier>CODEN: AJRBEL</identifier><language>eng</language><publisher>New York, NY: American Lung Association</publisher><subject>Air breathing ; Animals ; Biological and medical sciences ; Blotting, Northern ; Cells, Cultured ; Collagen - metabolism ; Collagenases - metabolism ; Female ; Fetus ; Fundamental and applied biological sciences. Psychology ; Lung - cytology ; Lung - embryology ; Lung - metabolism ; Lung - ultrastructure ; Pregnancy ; Rats ; Rats, Sprague-Dawley ; Respiratory system: anatomy, metabolism, gas exchange, ventilatory mechanics, respiratory hemodynamics ; Vertebrates: respiratory system</subject><ispartof>American journal of respiratory cell and molecular biology, 1993-07, Vol.9 (1), p.99-105</ispartof><rights>1994 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c317t-2d3817aca8f592b3f28086ad71bd7783f6bcea5f4371268ecbb7e3579a7327373</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=3770255$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8338680$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ARDEN, M. G</creatorcontrib><creatorcontrib>SPEARMAN, M. A</creatorcontrib><creatorcontrib>ADAMSON, I. Y. R</creatorcontrib><title>Degradation of type IV collagen during the development of fetal rat lung</title><title>American journal of respiratory cell and molecular biology</title><addtitle>Am J Respir Cell Mol Biol</addtitle><description>Lung structure undergoes rapid remodeling during late gestation as a functional respiratory unit is formed. To determine the role of collagen turnover in this process, particularly the basement membrane component, we studied the degradation of collagen in a series of fetal rats from day 18 of gestation to full term. During the period of rapid cell proliferation to day 20, the collagen level per milligram of lung did not change though the rate of synthesis increased. More than 40% of new collagen was rapidly degraded. At the end of the growth phase, collagen synthesis rose rapidly as the total collagen content increased in the lung. Over this period, little Type I collagenase activity could be detected, but degradation of Type IV collagen was readily measured and was maximal at 18 to 20 days. The enzyme(s) was almost all present in the active form, and evidence for dissolution of the subepithelial basement membrane was also found by electron microscopy. Using isolated fetal epithelial cells and fibroblasts, supernatants of both cell types showed degradative activity for Type IV collagen, particularly at days 18 to 20. The major enzyme involved appears to be a 72 kD collagenase, as shown by zymography and by mRNA expression in both cell types. The results demonstrate that rapid degradation of Type IV collagen occurs during the growth phase of late fetal lung development, and that both epithelial and stromal cells contribute to collagenolytic activity.</description><subject>Air breathing</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>Cells, Cultured</subject><subject>Collagen - metabolism</subject><subject>Collagenases - metabolism</subject><subject>Female</subject><subject>Fetus</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Lung - cytology</subject><subject>Lung - embryology</subject><subject>Lung - metabolism</subject><subject>Lung - ultrastructure</subject><subject>Pregnancy</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Respiratory system: anatomy, metabolism, gas exchange, ventilatory mechanics, respiratory hemodynamics</subject><subject>Vertebrates: respiratory system</subject><issn>1044-1549</issn><issn>1535-4989</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1993</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kM1LwzAYxoMoc06PHoUcxFu3pmma5CjzY4OBF_Ua0vRN7eiXSSrsv7djZaf3gefHw8sPoXsSLwnJ2ErvnWnylVySpZQXaE4YZVEqhbwcc5ymEWGpvEY33u_jmCSCkBmaCUpFJuI52rxA6XShQ9W1uLM4HHrA229surrWJbS4GFzVljj8AC7gD-qub6ANR9RC0DV2OuB6aMtbdGV17eFuugv09fb6ud5Eu4_37fp5FxlKeIiSggrCtdHCMpnk1CYiFpkuOMkLzgW1WW5AM5tSTpJMgMlzDpRxqTlNOOV0gZ5Ou73rfgfwQTWVNzB-20I3eMWZYFkqkhGMTqBxnfcOrOpd1Wh3UCRWR3PqZE5JRZSUI_8wDQ95A8WZnlSN_ePUa290bZ1uTeXPGOU8Thij_zm1duI</recordid><startdate>19930701</startdate><enddate>19930701</enddate><creator>ARDEN, M. G</creator><creator>SPEARMAN, M. A</creator><creator>ADAMSON, I. Y. R</creator><general>American Lung Association</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>19930701</creationdate><title>Degradation of type IV collagen during the development of fetal rat lung</title><author>ARDEN, M. G ; SPEARMAN, M. A ; ADAMSON, I. Y. R</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c317t-2d3817aca8f592b3f28086ad71bd7783f6bcea5f4371268ecbb7e3579a7327373</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1993</creationdate><topic>Air breathing</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>Cells, Cultured</topic><topic>Collagen - metabolism</topic><topic>Collagenases - metabolism</topic><topic>Female</topic><topic>Fetus</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Lung - cytology</topic><topic>Lung - embryology</topic><topic>Lung - metabolism</topic><topic>Lung - ultrastructure</topic><topic>Pregnancy</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Respiratory system: anatomy, metabolism, gas exchange, ventilatory mechanics, respiratory hemodynamics</topic><topic>Vertebrates: respiratory system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ARDEN, M. G</creatorcontrib><creatorcontrib>SPEARMAN, M. A</creatorcontrib><creatorcontrib>ADAMSON, I. Y. R</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>American journal of respiratory cell and molecular biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ARDEN, M. G</au><au>SPEARMAN, M. A</au><au>ADAMSON, I. Y. R</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Degradation of type IV collagen during the development of fetal rat lung</atitle><jtitle>American journal of respiratory cell and molecular biology</jtitle><addtitle>Am J Respir Cell Mol Biol</addtitle><date>1993-07-01</date><risdate>1993</risdate><volume>9</volume><issue>1</issue><spage>99</spage><epage>105</epage><pages>99-105</pages><issn>1044-1549</issn><eissn>1535-4989</eissn><coden>AJRBEL</coden><abstract>Lung structure undergoes rapid remodeling during late gestation as a functional respiratory unit is formed. To determine the role of collagen turnover in this process, particularly the basement membrane component, we studied the degradation of collagen in a series of fetal rats from day 18 of gestation to full term. During the period of rapid cell proliferation to day 20, the collagen level per milligram of lung did not change though the rate of synthesis increased. More than 40% of new collagen was rapidly degraded. At the end of the growth phase, collagen synthesis rose rapidly as the total collagen content increased in the lung. Over this period, little Type I collagenase activity could be detected, but degradation of Type IV collagen was readily measured and was maximal at 18 to 20 days. The enzyme(s) was almost all present in the active form, and evidence for dissolution of the subepithelial basement membrane was also found by electron microscopy. Using isolated fetal epithelial cells and fibroblasts, supernatants of both cell types showed degradative activity for Type IV collagen, particularly at days 18 to 20. The major enzyme involved appears to be a 72 kD collagenase, as shown by zymography and by mRNA expression in both cell types. The results demonstrate that rapid degradation of Type IV collagen occurs during the growth phase of late fetal lung development, and that both epithelial and stromal cells contribute to collagenolytic activity.</abstract><cop>New York, NY</cop><pub>American Lung Association</pub><pmid>8338680</pmid><doi>10.1165/ajrcmb/9.1.99</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1044-1549
ispartof American journal of respiratory cell and molecular biology, 1993-07, Vol.9 (1), p.99-105
issn 1044-1549
1535-4989
language eng
recordid cdi_proquest_miscellaneous_75856482
source MEDLINE; Journals@Ovid Complete
subjects Air breathing
Animals
Biological and medical sciences
Blotting, Northern
Cells, Cultured
Collagen - metabolism
Collagenases - metabolism
Female
Fetus
Fundamental and applied biological sciences. Psychology
Lung - cytology
Lung - embryology
Lung - metabolism
Lung - ultrastructure
Pregnancy
Rats
Rats, Sprague-Dawley
Respiratory system: anatomy, metabolism, gas exchange, ventilatory mechanics, respiratory hemodynamics
Vertebrates: respiratory system
title Degradation of type IV collagen during the development of fetal rat lung
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-06T16%3A00%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Degradation%20of%20type%20IV%20collagen%20during%20the%20development%20of%20fetal%20rat%20lung&rft.jtitle=American%20journal%20of%20respiratory%20cell%20and%20molecular%20biology&rft.au=ARDEN,%20M.%20G&rft.date=1993-07-01&rft.volume=9&rft.issue=1&rft.spage=99&rft.epage=105&rft.pages=99-105&rft.issn=1044-1549&rft.eissn=1535-4989&rft.coden=AJRBEL&rft_id=info:doi/10.1165/ajrcmb/9.1.99&rft_dat=%3Cproquest_cross%3E75856482%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=75856482&rft_id=info:pmid/8338680&rfr_iscdi=true