Assessment of subacute inflammatory and proliferative response to coronary stenting in a porcine model by local gene expression studies and histomorphometry
The aim of the study was to analyse inflammatory and proliferative response early after coronary stenting by angiography, histomorphometry and local gene expression analysis using quantitative rt-PCR. Therefore, eight German domestic pigs underwent stenting of the left coronary artery. Selective cor...
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Veröffentlicht in: | Biomaterials 2004-03, Vol.25 (6), p.957-963 |
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description | The aim of the study was to analyse inflammatory and proliferative response early after coronary stenting by angiography, histomorphometry and local gene expression analysis using quantitative rt-PCR. Therefore, eight German domestic pigs underwent stenting of the left coronary artery. Selective coronary angiography was performed after 14 days. Explanted coronary arteries were examined histomorphometrically after methacrylate-embedding. Snap-frozen samples were examined for local gene expression of TGF-
β, TNF-
α, GM-CSF, VEGF, PDGF and Fas Ligand (FasL) by real-time quantitative rt-PCR normalized to the housekeeping gene GAPDH and compared to unstented coronary arteries. All stented coronaries were patent with only little neointima formation. The median vessel diameter was 2.55
mm (range 2.43–2.68
mm). Histopathology revealed little inflammatory response limited to the tissue surrounding the stent struts; luminal area ranged from 84% to 91%. Compared to unstented control arteries, no significant differences in local gene expression were detected for VEGF, PDGF, TGF-
β, TNF-
α and GM-CSF. Expression of FasL was upregulated as little as 1.7-fold (
p=0.01). We conclude that, in native coronary arteries, no significant upregulation of investigated genes regulating vascular remodelling, inflammation or fibrogenesis was demonstrated 14 days after stenting. Whether upregulation of FasL as a marker gene of apoptosis is transient and biological significant requires further investigation. |
doi_str_mv | 10.1016/S0142-9612(03)00613-6 |
format | Article |
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β, TNF-
α, GM-CSF, VEGF, PDGF and Fas Ligand (FasL) by real-time quantitative rt-PCR normalized to the housekeeping gene GAPDH and compared to unstented coronary arteries. All stented coronaries were patent with only little neointima formation. The median vessel diameter was 2.55
mm (range 2.43–2.68
mm). Histopathology revealed little inflammatory response limited to the tissue surrounding the stent struts; luminal area ranged from 84% to 91%. Compared to unstented control arteries, no significant differences in local gene expression were detected for VEGF, PDGF, TGF-
β, TNF-
α and GM-CSF. Expression of FasL was upregulated as little as 1.7-fold (
p=0.01). We conclude that, in native coronary arteries, no significant upregulation of investigated genes regulating vascular remodelling, inflammation or fibrogenesis was demonstrated 14 days after stenting. Whether upregulation of FasL as a marker gene of apoptosis is transient and biological significant requires further investigation.</description><identifier>ISSN: 0142-9612</identifier><identifier>EISSN: 1878-5905</identifier><identifier>DOI: 10.1016/S0142-9612(03)00613-6</identifier><identifier>PMID: 14615159</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Animals ; Apoptosis ; Arteries - metabolism ; Arteries - pathology ; Arteries - surgery ; Arteritis - diagnostic imaging ; Arteritis - etiology ; Arteritis - metabolism ; Arteritis - pathology ; Biocompatibility ; Blood Vessel Prosthesis - adverse effects ; Coronary Angiography ; Coronary Vessels - metabolism ; Coronary Vessels - pathology ; Coronary Vessels - surgery ; Cytokine ; Cytokines - metabolism ; Equipment Failure Analysis ; Gene expression ; Gene Expression Regulation ; Intravascular stent ; PCR ; Prosthesis-Related Infections - diagnostic imaging ; Prosthesis-Related Infections - etiology ; Prosthesis-Related Infections - metabolism ; Prosthesis-Related Infections - pathology ; Stents - adverse effects ; Swine, Miniature</subject><ispartof>Biomaterials, 2004-03, Vol.25 (6), p.957-963</ispartof><rights>2003 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c423t-2cbd93a80940463a8213cadc0c1f4608c585485e5fb112fdd8881bb0ab114aa03</citedby><cites>FETCH-LOGICAL-c423t-2cbd93a80940463a8213cadc0c1f4608c585485e5fb112fdd8881bb0ab114aa03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/S0142-9612(03)00613-6$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3548,27922,27923,45993</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/14615159$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Peuster, Matthias</creatorcontrib><creatorcontrib>Fink, Christoph</creatorcontrib><creatorcontrib>Reckers, Julia</creatorcontrib><creatorcontrib>Beerbaum, Philip</creatorcontrib><creatorcontrib>von Schnakenburg, Christian</creatorcontrib><title>Assessment of subacute inflammatory and proliferative response to coronary stenting in a porcine model by local gene expression studies and histomorphometry</title><title>Biomaterials</title><addtitle>Biomaterials</addtitle><description>The aim of the study was to analyse inflammatory and proliferative response early after coronary stenting by angiography, histomorphometry and local gene expression analysis using quantitative rt-PCR. Therefore, eight German domestic pigs underwent stenting of the left coronary artery. Selective coronary angiography was performed after 14 days. Explanted coronary arteries were examined histomorphometrically after methacrylate-embedding. Snap-frozen samples were examined for local gene expression of TGF-
β, TNF-
α, GM-CSF, VEGF, PDGF and Fas Ligand (FasL) by real-time quantitative rt-PCR normalized to the housekeeping gene GAPDH and compared to unstented coronary arteries. All stented coronaries were patent with only little neointima formation. The median vessel diameter was 2.55
mm (range 2.43–2.68
mm). Histopathology revealed little inflammatory response limited to the tissue surrounding the stent struts; luminal area ranged from 84% to 91%. Compared to unstented control arteries, no significant differences in local gene expression were detected for VEGF, PDGF, TGF-
β, TNF-
α and GM-CSF. Expression of FasL was upregulated as little as 1.7-fold (
p=0.01). We conclude that, in native coronary arteries, no significant upregulation of investigated genes regulating vascular remodelling, inflammation or fibrogenesis was demonstrated 14 days after stenting. Whether upregulation of FasL as a marker gene of apoptosis is transient and biological significant requires further investigation.</description><subject>Animals</subject><subject>Apoptosis</subject><subject>Arteries - metabolism</subject><subject>Arteries - pathology</subject><subject>Arteries - surgery</subject><subject>Arteritis - diagnostic imaging</subject><subject>Arteritis - etiology</subject><subject>Arteritis - metabolism</subject><subject>Arteritis - pathology</subject><subject>Biocompatibility</subject><subject>Blood Vessel Prosthesis - adverse effects</subject><subject>Coronary Angiography</subject><subject>Coronary Vessels - metabolism</subject><subject>Coronary Vessels - pathology</subject><subject>Coronary Vessels - surgery</subject><subject>Cytokine</subject><subject>Cytokines - metabolism</subject><subject>Equipment Failure Analysis</subject><subject>Gene expression</subject><subject>Gene Expression Regulation</subject><subject>Intravascular stent</subject><subject>PCR</subject><subject>Prosthesis-Related Infections - diagnostic imaging</subject><subject>Prosthesis-Related Infections - etiology</subject><subject>Prosthesis-Related Infections - metabolism</subject><subject>Prosthesis-Related Infections - pathology</subject><subject>Stents - adverse effects</subject><subject>Swine, Miniature</subject><issn>0142-9612</issn><issn>1878-5905</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkcFu1DAQhi0EotvCI4B8QnAI2I7tdU6oqqAgVeIAnC3HnrRGSRw8TtV9Fx4Wd3cFxz3ZM_r-fzTzE_KKs_eccf3hO-NSNJ3m4i1r3zGmedvoJ2TDzdY0qmPqKdn8Q87IOeIvVmsmxXNyxqXmiqtuQ_5cIgLiBHOhaaC49s6vBWich9FNkysp76ibA11yGuMA2ZV4DzQDLmlGoCVRn3KaXcWwVJc431YxdXRJ2ccZ6JQCjLTf0TF5N9JbqD14WKoDxjRX0Roi4H7GXcSSppSXuzRBybsX5NngRoSXx_eC_Pz86cfVl-bm2_XXq8ubxkvRlkb4PnStM6yr6-n6Ebz1Lnjm-SA1M14ZJY0CNfSciyEEYwzve-ZqKZ1j7QV5c_CtS_5eAYudInoYRzdDWtFuuVJcC3ESFEayVsjTjrzj2myVrKA6gD4nxAyDXXKc6jUtZ_YxaLsP2j6maFlr90FbXXWvjwPWfoLwX3VMtgIfDwDUw91HyBZ9hNlDiBl8sSHFEyP-AiH_u-k</recordid><startdate>20040301</startdate><enddate>20040301</enddate><creator>Peuster, Matthias</creator><creator>Fink, Christoph</creator><creator>Reckers, Julia</creator><creator>Beerbaum, Philip</creator><creator>von Schnakenburg, Christian</creator><general>Elsevier Ltd</general><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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>F28</scope><scope>7X8</scope></search><sort><creationdate>20040301</creationdate><title>Assessment of subacute inflammatory and proliferative response to coronary stenting in a porcine model by local gene expression studies and histomorphometry</title><author>Peuster, Matthias ; Fink, Christoph ; Reckers, Julia ; Beerbaum, Philip ; von Schnakenburg, Christian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c423t-2cbd93a80940463a8213cadc0c1f4608c585485e5fb112fdd8881bb0ab114aa03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Animals</topic><topic>Apoptosis</topic><topic>Arteries - metabolism</topic><topic>Arteries - pathology</topic><topic>Arteries - surgery</topic><topic>Arteritis - diagnostic imaging</topic><topic>Arteritis - etiology</topic><topic>Arteritis - metabolism</topic><topic>Arteritis - pathology</topic><topic>Biocompatibility</topic><topic>Blood Vessel Prosthesis - adverse effects</topic><topic>Coronary Angiography</topic><topic>Coronary Vessels - metabolism</topic><topic>Coronary Vessels - pathology</topic><topic>Coronary Vessels - surgery</topic><topic>Cytokine</topic><topic>Cytokines - metabolism</topic><topic>Equipment Failure Analysis</topic><topic>Gene expression</topic><topic>Gene Expression Regulation</topic><topic>Intravascular stent</topic><topic>PCR</topic><topic>Prosthesis-Related Infections - diagnostic imaging</topic><topic>Prosthesis-Related Infections - etiology</topic><topic>Prosthesis-Related Infections - metabolism</topic><topic>Prosthesis-Related Infections - pathology</topic><topic>Stents - adverse effects</topic><topic>Swine, Miniature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Peuster, Matthias</creatorcontrib><creatorcontrib>Fink, Christoph</creatorcontrib><creatorcontrib>Reckers, Julia</creatorcontrib><creatorcontrib>Beerbaum, Philip</creatorcontrib><creatorcontrib>von Schnakenburg, Christian</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>MEDLINE - Academic</collection><jtitle>Biomaterials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Peuster, Matthias</au><au>Fink, Christoph</au><au>Reckers, Julia</au><au>Beerbaum, Philip</au><au>von Schnakenburg, Christian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Assessment of subacute inflammatory and proliferative response to coronary stenting in a porcine model by local gene expression studies and histomorphometry</atitle><jtitle>Biomaterials</jtitle><addtitle>Biomaterials</addtitle><date>2004-03-01</date><risdate>2004</risdate><volume>25</volume><issue>6</issue><spage>957</spage><epage>963</epage><pages>957-963</pages><issn>0142-9612</issn><eissn>1878-5905</eissn><abstract>The aim of the study was to analyse inflammatory and proliferative response early after coronary stenting by angiography, histomorphometry and local gene expression analysis using quantitative rt-PCR. Therefore, eight German domestic pigs underwent stenting of the left coronary artery. Selective coronary angiography was performed after 14 days. Explanted coronary arteries were examined histomorphometrically after methacrylate-embedding. Snap-frozen samples were examined for local gene expression of TGF-
β, TNF-
α, GM-CSF, VEGF, PDGF and Fas Ligand (FasL) by real-time quantitative rt-PCR normalized to the housekeeping gene GAPDH and compared to unstented coronary arteries. All stented coronaries were patent with only little neointima formation. The median vessel diameter was 2.55
mm (range 2.43–2.68
mm). Histopathology revealed little inflammatory response limited to the tissue surrounding the stent struts; luminal area ranged from 84% to 91%. Compared to unstented control arteries, no significant differences in local gene expression were detected for VEGF, PDGF, TGF-
β, TNF-
α and GM-CSF. Expression of FasL was upregulated as little as 1.7-fold (
p=0.01). We conclude that, in native coronary arteries, no significant upregulation of investigated genes regulating vascular remodelling, inflammation or fibrogenesis was demonstrated 14 days after stenting. Whether upregulation of FasL as a marker gene of apoptosis is transient and biological significant requires further investigation.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>14615159</pmid><doi>10.1016/S0142-9612(03)00613-6</doi><tpages>7</tpages></addata></record> |
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subjects | Animals Apoptosis Arteries - metabolism Arteries - pathology Arteries - surgery Arteritis - diagnostic imaging Arteritis - etiology Arteritis - metabolism Arteritis - pathology Biocompatibility Blood Vessel Prosthesis - adverse effects Coronary Angiography Coronary Vessels - metabolism Coronary Vessels - pathology Coronary Vessels - surgery Cytokine Cytokines - metabolism Equipment Failure Analysis Gene expression Gene Expression Regulation Intravascular stent PCR Prosthesis-Related Infections - diagnostic imaging Prosthesis-Related Infections - etiology Prosthesis-Related Infections - metabolism Prosthesis-Related Infections - pathology Stents - adverse effects Swine, Miniature |
title | Assessment of subacute inflammatory and proliferative response to coronary stenting in a porcine model by local gene expression studies and histomorphometry |
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