Neointimal Hyperplasia after Stenting in a Human Mammary Artery Organ Culture
Although the use of stents has limited the incidence of restenosis, in-stent restenosis remains an important problem. In-stent restenosis is the result of a healing process that induced neointimal hyperplasia through mechanisms that are still not understood. The aim of this study was to analyze the...
Gespeichert in:
Veröffentlicht in: | Journal of vascular research 2004-01, Vol.41 (1), p.46-53 |
---|---|
Hauptverfasser: | , , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 53 |
---|---|
container_issue | 1 |
container_start_page | 46 |
container_title | Journal of vascular research |
container_volume | 41 |
creator | Guérin, P. Rondeau, F. Grimandi, G. Heymann, M.F. Heymann, D. Pillet, P. Al Habash, O. Loirand, G. Pacaud, P. Crochet, D. |
description | Although the use of stents has limited the incidence of restenosis, in-stent restenosis remains an important problem. In-stent restenosis is the result of a healing process that induced neointimal hyperplasia through mechanisms that are still not understood. The aim of this study was to analyze the histological consequences of the healing process following stent implantation. Internal mammary arteries from atheroslerotic patients undergoing coronary artery bypass surgery were stented and maintained in culture for 0–28 days. Stent implantation after predilatation induced an extensive loss of endothelial cells whereas direct stenting preserved endothelium between the struts. Morphometric analysis shows that stent placement induced neointimal thickening. Smooth muscle α-actin labeling indicates that neo-intimal formation was mainly due to proliferation and migration of smooth muscle cells. Smooth muscle cell proliferation, assessed by MIB-1 staining, was maximal at day 14 after stent insertion. Human mammary artery organ culture thus provides valuable information on histological consequences of stent implantation with or without predilatation regarding endothelial cell disappearance and neointimal hyperplasia. These data also demonstrate that neointimal thickening induced by stent implantation comprises an intrinsic component resulting from the vessel wall response to stent insertion and suggest that blood factors could play an amplifying but not necessary role. |
doi_str_mv | 10.1159/000076245 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmed_primary_14730201</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>80167558</sourcerecordid><originalsourceid>FETCH-LOGICAL-c387t-a25174a5eca50194192fb8dce4a582d9912247a4899c1b07172dc8830751f08f3</originalsourceid><addsrcrecordid>eNpt0N1LHDEQAPAgLX6cfehzoYSDFvqwmskmm-RRjtpTTg-0-rrMZbPH2v0y2X24_97onQrFvCTM_JjJDCFfgZ0ASHPK4lEZF3KPHILgacIglZ_im4FOABQ_IEchPDAGwuhsnxyAUCnjDA7J1bXrqnaoGqzpfNM739cYKqRYDs7T28HFXLumVUuRzscGW3qFTYN-Q898FBu69OsYnI31MHp3TD6XWAf3ZXdPyN3577-zebJY_rmYnS0Sm2o1JMglKIHSWZQMjADDy5UurIsxzQtjgHOhUGhjLKyYihMUVuuUKQkl02U6IT-3dXvfPY4uDHlTBevqGlvXjSHXDDIlpY5w-h986Ebfxr_lsYUUWQYiol9bZH0Xgndl3vvqecYcWP684PxtwdF-3xUcV40r3uVuoxH82AEMFuvSY2ur8O6kBIDMRPdt6_6hXzv_Bl7bTD_MXt7fvIC8L8r0CcImlDs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>224546614</pqid></control><display><type>article</type><title>Neointimal Hyperplasia after Stenting in a Human Mammary Artery Organ Culture</title><source>MEDLINE</source><source>Karger Journals</source><source>Alma/SFX Local Collection</source><creator>Guérin, P. ; Rondeau, F. ; Grimandi, G. ; Heymann, M.F. ; Heymann, D. ; Pillet, P. ; Al Habash, O. ; Loirand, G. ; Pacaud, P. ; Crochet, D.</creator><creatorcontrib>Guérin, P. ; Rondeau, F. ; Grimandi, G. ; Heymann, M.F. ; Heymann, D. ; Pillet, P. ; Al Habash, O. ; Loirand, G. ; Pacaud, P. ; Crochet, D.</creatorcontrib><description>Although the use of stents has limited the incidence of restenosis, in-stent restenosis remains an important problem. In-stent restenosis is the result of a healing process that induced neointimal hyperplasia through mechanisms that are still not understood. The aim of this study was to analyze the histological consequences of the healing process following stent implantation. Internal mammary arteries from atheroslerotic patients undergoing coronary artery bypass surgery were stented and maintained in culture for 0–28 days. Stent implantation after predilatation induced an extensive loss of endothelial cells whereas direct stenting preserved endothelium between the struts. Morphometric analysis shows that stent placement induced neointimal thickening. Smooth muscle α-actin labeling indicates that neo-intimal formation was mainly due to proliferation and migration of smooth muscle cells. Smooth muscle cell proliferation, assessed by MIB-1 staining, was maximal at day 14 after stent insertion. Human mammary artery organ culture thus provides valuable information on histological consequences of stent implantation with or without predilatation regarding endothelial cell disappearance and neointimal hyperplasia. These data also demonstrate that neointimal thickening induced by stent implantation comprises an intrinsic component resulting from the vessel wall response to stent insertion and suggest that blood factors could play an amplifying but not necessary role.</description><identifier>ISSN: 1018-1172</identifier><identifier>EISSN: 1423-0135</identifier><identifier>DOI: 10.1159/000076245</identifier><identifier>PMID: 14730201</identifier><identifier>CODEN: JVREE9</identifier><language>eng</language><publisher>Basel, Switzerland: Karger</publisher><subject>Atherosclerosis (general aspects, experimental research) ; Biological and medical sciences ; Blood and lymphatic vessels ; Cardiology. Vascular system ; Cell Division ; Coronary Restenosis ; Endothelium, Vascular - pathology ; Fundamental and applied biological sciences. Psychology ; Humans ; Hyperplasia ; Mammary Arteries - pathology ; Medical sciences ; Organ Culture Techniques ; Research Paper ; Stents ; Tunica Intima - pathology ; Vertebrates: cardiovascular system</subject><ispartof>Journal of vascular research, 2004-01, Vol.41 (1), p.46-53</ispartof><rights>2004 S. Karger AG, Basel</rights><rights>2004 INIST-CNRS</rights><rights>Copyright 2004 S. Karger AG, Basel</rights><rights>Copyright (c) 2004 S. Karger AG, Basel</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-a25174a5eca50194192fb8dce4a582d9912247a4899c1b07172dc8830751f08f3</citedby><cites>FETCH-LOGICAL-c387t-a25174a5eca50194192fb8dce4a582d9912247a4899c1b07172dc8830751f08f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2427,4021,27921,27922,27923</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=15511169$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14730201$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guérin, P.</creatorcontrib><creatorcontrib>Rondeau, F.</creatorcontrib><creatorcontrib>Grimandi, G.</creatorcontrib><creatorcontrib>Heymann, M.F.</creatorcontrib><creatorcontrib>Heymann, D.</creatorcontrib><creatorcontrib>Pillet, P.</creatorcontrib><creatorcontrib>Al Habash, O.</creatorcontrib><creatorcontrib>Loirand, G.</creatorcontrib><creatorcontrib>Pacaud, P.</creatorcontrib><creatorcontrib>Crochet, D.</creatorcontrib><title>Neointimal Hyperplasia after Stenting in a Human Mammary Artery Organ Culture</title><title>Journal of vascular research</title><addtitle>J Vasc Res</addtitle><description>Although the use of stents has limited the incidence of restenosis, in-stent restenosis remains an important problem. In-stent restenosis is the result of a healing process that induced neointimal hyperplasia through mechanisms that are still not understood. The aim of this study was to analyze the histological consequences of the healing process following stent implantation. Internal mammary arteries from atheroslerotic patients undergoing coronary artery bypass surgery were stented and maintained in culture for 0–28 days. Stent implantation after predilatation induced an extensive loss of endothelial cells whereas direct stenting preserved endothelium between the struts. Morphometric analysis shows that stent placement induced neointimal thickening. Smooth muscle α-actin labeling indicates that neo-intimal formation was mainly due to proliferation and migration of smooth muscle cells. Smooth muscle cell proliferation, assessed by MIB-1 staining, was maximal at day 14 after stent insertion. Human mammary artery organ culture thus provides valuable information on histological consequences of stent implantation with or without predilatation regarding endothelial cell disappearance and neointimal hyperplasia. These data also demonstrate that neointimal thickening induced by stent implantation comprises an intrinsic component resulting from the vessel wall response to stent insertion and suggest that blood factors could play an amplifying but not necessary role.</description><subject>Atherosclerosis (general aspects, experimental research)</subject><subject>Biological and medical sciences</subject><subject>Blood and lymphatic vessels</subject><subject>Cardiology. Vascular system</subject><subject>Cell Division</subject><subject>Coronary Restenosis</subject><subject>Endothelium, Vascular - pathology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>Hyperplasia</subject><subject>Mammary Arteries - pathology</subject><subject>Medical sciences</subject><subject>Organ Culture Techniques</subject><subject>Research Paper</subject><subject>Stents</subject><subject>Tunica Intima - pathology</subject><subject>Vertebrates: cardiovascular system</subject><issn>1018-1172</issn><issn>1423-0135</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><recordid>eNpt0N1LHDEQAPAgLX6cfehzoYSDFvqwmskmm-RRjtpTTg-0-rrMZbPH2v0y2X24_97onQrFvCTM_JjJDCFfgZ0ASHPK4lEZF3KPHILgacIglZ_im4FOABQ_IEchPDAGwuhsnxyAUCnjDA7J1bXrqnaoGqzpfNM739cYKqRYDs7T28HFXLumVUuRzscGW3qFTYN-Q898FBu69OsYnI31MHp3TD6XWAf3ZXdPyN3577-zebJY_rmYnS0Sm2o1JMglKIHSWZQMjADDy5UurIsxzQtjgHOhUGhjLKyYihMUVuuUKQkl02U6IT-3dXvfPY4uDHlTBevqGlvXjSHXDDIlpY5w-h986Ebfxr_lsYUUWQYiol9bZH0Xgndl3vvqecYcWP684PxtwdF-3xUcV40r3uVuoxH82AEMFuvSY2ur8O6kBIDMRPdt6_6hXzv_Bl7bTD_MXt7fvIC8L8r0CcImlDs</recordid><startdate>200401</startdate><enddate>200401</enddate><creator>Guérin, P.</creator><creator>Rondeau, F.</creator><creator>Grimandi, G.</creator><creator>Heymann, M.F.</creator><creator>Heymann, D.</creator><creator>Pillet, P.</creator><creator>Al Habash, O.</creator><creator>Loirand, G.</creator><creator>Pacaud, P.</creator><creator>Crochet, D.</creator><general>Karger</general><general>S. Karger AG</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>3V.</scope><scope>7QL</scope><scope>7T7</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2P</scope><scope>M7N</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>200401</creationdate><title>Neointimal Hyperplasia after Stenting in a Human Mammary Artery Organ Culture</title><author>Guérin, P. ; Rondeau, F. ; Grimandi, G. ; Heymann, M.F. ; Heymann, D. ; Pillet, P. ; Al Habash, O. ; Loirand, G. ; Pacaud, P. ; Crochet, D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-a25174a5eca50194192fb8dce4a582d9912247a4899c1b07172dc8830751f08f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Atherosclerosis (general aspects, experimental research)</topic><topic>Biological and medical sciences</topic><topic>Blood and lymphatic vessels</topic><topic>Cardiology. Vascular system</topic><topic>Cell Division</topic><topic>Coronary Restenosis</topic><topic>Endothelium, Vascular - pathology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Humans</topic><topic>Hyperplasia</topic><topic>Mammary Arteries - pathology</topic><topic>Medical sciences</topic><topic>Organ Culture Techniques</topic><topic>Research Paper</topic><topic>Stents</topic><topic>Tunica Intima - pathology</topic><topic>Vertebrates: cardiovascular system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guérin, P.</creatorcontrib><creatorcontrib>Rondeau, F.</creatorcontrib><creatorcontrib>Grimandi, G.</creatorcontrib><creatorcontrib>Heymann, M.F.</creatorcontrib><creatorcontrib>Heymann, D.</creatorcontrib><creatorcontrib>Pillet, P.</creatorcontrib><creatorcontrib>Al Habash, O.</creatorcontrib><creatorcontrib>Loirand, G.</creatorcontrib><creatorcontrib>Pacaud, P.</creatorcontrib><creatorcontrib>Crochet, D.</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>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Science Database (Alumni Edition)</collection><collection>STEM Database</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Science Database</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>SIRS Editorial</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of vascular research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guérin, P.</au><au>Rondeau, F.</au><au>Grimandi, G.</au><au>Heymann, M.F.</au><au>Heymann, D.</au><au>Pillet, P.</au><au>Al Habash, O.</au><au>Loirand, G.</au><au>Pacaud, P.</au><au>Crochet, D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neointimal Hyperplasia after Stenting in a Human Mammary Artery Organ Culture</atitle><jtitle>Journal of vascular research</jtitle><addtitle>J Vasc Res</addtitle><date>2004-01</date><risdate>2004</risdate><volume>41</volume><issue>1</issue><spage>46</spage><epage>53</epage><pages>46-53</pages><issn>1018-1172</issn><eissn>1423-0135</eissn><coden>JVREE9</coden><abstract>Although the use of stents has limited the incidence of restenosis, in-stent restenosis remains an important problem. In-stent restenosis is the result of a healing process that induced neointimal hyperplasia through mechanisms that are still not understood. The aim of this study was to analyze the histological consequences of the healing process following stent implantation. Internal mammary arteries from atheroslerotic patients undergoing coronary artery bypass surgery were stented and maintained in culture for 0–28 days. Stent implantation after predilatation induced an extensive loss of endothelial cells whereas direct stenting preserved endothelium between the struts. Morphometric analysis shows that stent placement induced neointimal thickening. Smooth muscle α-actin labeling indicates that neo-intimal formation was mainly due to proliferation and migration of smooth muscle cells. Smooth muscle cell proliferation, assessed by MIB-1 staining, was maximal at day 14 after stent insertion. Human mammary artery organ culture thus provides valuable information on histological consequences of stent implantation with or without predilatation regarding endothelial cell disappearance and neointimal hyperplasia. These data also demonstrate that neointimal thickening induced by stent implantation comprises an intrinsic component resulting from the vessel wall response to stent insertion and suggest that blood factors could play an amplifying but not necessary role.</abstract><cop>Basel, Switzerland</cop><pub>Karger</pub><pmid>14730201</pmid><doi>10.1159/000076245</doi><tpages>8</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1018-1172 |
ispartof | Journal of vascular research, 2004-01, Vol.41 (1), p.46-53 |
issn | 1018-1172 1423-0135 |
language | eng |
recordid | cdi_pubmed_primary_14730201 |
source | MEDLINE; Karger Journals; Alma/SFX Local Collection |
subjects | Atherosclerosis (general aspects, experimental research) Biological and medical sciences Blood and lymphatic vessels Cardiology. Vascular system Cell Division Coronary Restenosis Endothelium, Vascular - pathology Fundamental and applied biological sciences. Psychology Humans Hyperplasia Mammary Arteries - pathology Medical sciences Organ Culture Techniques Research Paper Stents Tunica Intima - pathology Vertebrates: cardiovascular system |
title | Neointimal Hyperplasia after Stenting in a Human Mammary Artery Organ Culture |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-13T22%3A18%3A00IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Neointimal%20Hyperplasia%20after%20Stenting%20in%20a%20Human%20Mammary%20Artery%20Organ%20Culture&rft.jtitle=Journal%20of%20vascular%20research&rft.au=Gu%C3%A9rin,%20P.&rft.date=2004-01&rft.volume=41&rft.issue=1&rft.spage=46&rft.epage=53&rft.pages=46-53&rft.issn=1018-1172&rft.eissn=1423-0135&rft.coden=JVREE9&rft_id=info:doi/10.1159/000076245&rft_dat=%3Cproquest_pubme%3E80167558%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=224546614&rft_id=info:pmid/14730201&rfr_iscdi=true |