Potent endothelial progenitor cell-conditioned media-related anti-apoptotic, cardiotrophic, and pro-angiogenic effects post-myocardial infarction are mediated by insulin-like growth factor-1
We have previously reported the cardioprotective effects of endothelial progenitor cell (EPC)-conditioned media (CM) therapy post-myocardial infarction (MI). In the present study, we have determined the insulin-like growth factor-1 (IGF-1) contribution to EPC CM effects on cardiomyocyte survival, co...
Gespeichert in:
Veröffentlicht in: | European heart journal 2013-03, Vol.34 (10), p.782-789 |
---|---|
Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 789 |
---|---|
container_issue | 10 |
container_start_page | 782 |
container_title | European heart journal |
container_volume | 34 |
creator | Hynes, Brian Kumar, Arun H S O'Sullivan, John Klein Buneker, Chirlei Leblond, Anne-Laure Weiss, Sharon Schmeckpeper, Jeffrey Martin, Kenneth Caplice, Noel M |
description | We have previously reported the cardioprotective effects of endothelial progenitor cell (EPC)-conditioned media (CM) therapy post-myocardial infarction (MI). In the present study, we have determined the insulin-like growth factor-1 (IGF-1) contribution to EPC CM effects on cardiomyocyte survival, contractility, and angiogenesis in vivo.
Conditioned media from porcine EPC were administered intracoronary in the presence and absence of specific neutralizing antibodies to IGF-1 or control IgG in a porcine model of MI. X-vivo (non-conditioned) medium was used as a control. Functional, histological, and biochemical parameters were evaluated at 24 h and 8-week post-therapy. Conditioned media therapy significantly abrogated infarct zone (IZ) apoptosis, hypocontractility, and impaired left ventricular (LV) relaxation observed in control infarcts acutely (24 h post-MI). At 8 weeks following treatment, CM therapy augmented LV contractility and relaxation, IZ angiogenesis and inhibited infarct size expansion, wall expansion, and wall thinning. All of these acute and chronic beneficial effects of CM therapy were vitiated by neutralizing antibodies to IGF-1 but not by control IgG. Moreover, the addition of neutralizing IGF-1 antibody to control medium had no effect on these structural or functional changes in the heart post-treatment.
Insulin-like growth factor-1 within the EPC CM mediates potent acute myocardial repair and chronic remodelling effects post-MI. These findings may provide a rationale for comparative trials of specific growth factors vs. current progenitor cell strategies. |
doi_str_mv | 10.1093/eurheartj/ehr435 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1315637207</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1315637207</sourcerecordid><originalsourceid>FETCH-LOGICAL-c407t-4a65fdea7fa72147807c11b60b953aa705c614563caaf0d35ae843c9fb9f35873</originalsourceid><addsrcrecordid>eNo9UUtv1DAQthAVXQp3TshHDpjacWwnR1SVh1QJDq3ELZo4441L1g62I7R_jt_WpFt6Go3me8zMR8g7wT8J3spLXNKIkMr9JY6pluoF2QlVVazVtXpJdly0imnd_Donr3O-55w3WuhX5LyqhJEtb3fk389YMBSKYYhlxMnDROcU9xh8iYlanCZmYxh88THgQA84eGAJJyhrB6F4BnOcSyzefqQW0uBjSXEetxbCsIkxCHv_KGkpOoe2ZDrHXNjhGB8Zq6cPDpLdTCgkPNlsDv1xHeVl8oFN_jfSfYp_y0gd2HU9Jt6QMwdTxrdP9YLcfbm-vfrGbn58_X71-YbZmpvCatDKDQjGgalEbRpurBC95n2rJIDhympRKy0tgOODVIBNLW3r-tZJ1Rh5QT6cdNdz_iyYS3fweXsOBIxL7oQUK9tUfIPyE9SmmHNC183JHyAdO8G7LbXuObXulNpKef-kvvTr5c-E_zHJB0_tnLM</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1315637207</pqid></control><display><type>article</type><title>Potent endothelial progenitor cell-conditioned media-related anti-apoptotic, cardiotrophic, and pro-angiogenic effects post-myocardial infarction are mediated by insulin-like growth factor-1</title><source>MEDLINE</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Hynes, Brian ; Kumar, Arun H S ; O'Sullivan, John ; Klein Buneker, Chirlei ; Leblond, Anne-Laure ; Weiss, Sharon ; Schmeckpeper, Jeffrey ; Martin, Kenneth ; Caplice, Noel M</creator><creatorcontrib>Hynes, Brian ; Kumar, Arun H S ; O'Sullivan, John ; Klein Buneker, Chirlei ; Leblond, Anne-Laure ; Weiss, Sharon ; Schmeckpeper, Jeffrey ; Martin, Kenneth ; Caplice, Noel M</creatorcontrib><description>We have previously reported the cardioprotective effects of endothelial progenitor cell (EPC)-conditioned media (CM) therapy post-myocardial infarction (MI). In the present study, we have determined the insulin-like growth factor-1 (IGF-1) contribution to EPC CM effects on cardiomyocyte survival, contractility, and angiogenesis in vivo.
Conditioned media from porcine EPC were administered intracoronary in the presence and absence of specific neutralizing antibodies to IGF-1 or control IgG in a porcine model of MI. X-vivo (non-conditioned) medium was used as a control. Functional, histological, and biochemical parameters were evaluated at 24 h and 8-week post-therapy. Conditioned media therapy significantly abrogated infarct zone (IZ) apoptosis, hypocontractility, and impaired left ventricular (LV) relaxation observed in control infarcts acutely (24 h post-MI). At 8 weeks following treatment, CM therapy augmented LV contractility and relaxation, IZ angiogenesis and inhibited infarct size expansion, wall expansion, and wall thinning. All of these acute and chronic beneficial effects of CM therapy were vitiated by neutralizing antibodies to IGF-1 but not by control IgG. Moreover, the addition of neutralizing IGF-1 antibody to control medium had no effect on these structural or functional changes in the heart post-treatment.
Insulin-like growth factor-1 within the EPC CM mediates potent acute myocardial repair and chronic remodelling effects post-MI. These findings may provide a rationale for comparative trials of specific growth factors vs. current progenitor cell strategies.</description><identifier>ISSN: 0195-668X</identifier><identifier>EISSN: 1522-9645</identifier><identifier>DOI: 10.1093/eurheartj/ehr435</identifier><identifier>PMID: 22173909</identifier><language>eng</language><publisher>England</publisher><subject>Animals ; Antibodies, Neutralizing - physiology ; Apoptosis - physiology ; Biomarkers - metabolism ; Cardiotonic Agents - pharmacology ; Cell Survival ; Culture Media, Conditioned - pharmacology ; Endothelial Cells - physiology ; Endothelial Cells - transplantation ; Female ; Heart Ventricles - pathology ; Insulin-Like Growth Factor I - antagonists & inhibitors ; Insulin-Like Growth Factor I - immunology ; Insulin-Like Growth Factor I - pharmacology ; Myocardial Contraction - physiology ; Myocardial Infarction - metabolism ; Myocardial Infarction - pathology ; Myocardial Infarction - therapy ; Myocytes, Cardiac - physiology ; Neovascularization, Physiologic - physiology ; Phosphorylation ; Proto-Oncogene Proteins c-akt - metabolism ; Stem Cell Transplantation - methods ; Stem Cells - physiology ; Sus scrofa ; Ventricular Dysfunction, Left - pathology ; Ventricular Dysfunction, Left - therapy</subject><ispartof>European heart journal, 2013-03, Vol.34 (10), p.782-789</ispartof><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c407t-4a65fdea7fa72147807c11b60b953aa705c614563caaf0d35ae843c9fb9f35873</citedby><cites>FETCH-LOGICAL-c407t-4a65fdea7fa72147807c11b60b953aa705c614563caaf0d35ae843c9fb9f35873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22173909$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hynes, Brian</creatorcontrib><creatorcontrib>Kumar, Arun H S</creatorcontrib><creatorcontrib>O'Sullivan, John</creatorcontrib><creatorcontrib>Klein Buneker, Chirlei</creatorcontrib><creatorcontrib>Leblond, Anne-Laure</creatorcontrib><creatorcontrib>Weiss, Sharon</creatorcontrib><creatorcontrib>Schmeckpeper, Jeffrey</creatorcontrib><creatorcontrib>Martin, Kenneth</creatorcontrib><creatorcontrib>Caplice, Noel M</creatorcontrib><title>Potent endothelial progenitor cell-conditioned media-related anti-apoptotic, cardiotrophic, and pro-angiogenic effects post-myocardial infarction are mediated by insulin-like growth factor-1</title><title>European heart journal</title><addtitle>Eur Heart J</addtitle><description>We have previously reported the cardioprotective effects of endothelial progenitor cell (EPC)-conditioned media (CM) therapy post-myocardial infarction (MI). In the present study, we have determined the insulin-like growth factor-1 (IGF-1) contribution to EPC CM effects on cardiomyocyte survival, contractility, and angiogenesis in vivo.
Conditioned media from porcine EPC were administered intracoronary in the presence and absence of specific neutralizing antibodies to IGF-1 or control IgG in a porcine model of MI. X-vivo (non-conditioned) medium was used as a control. Functional, histological, and biochemical parameters were evaluated at 24 h and 8-week post-therapy. Conditioned media therapy significantly abrogated infarct zone (IZ) apoptosis, hypocontractility, and impaired left ventricular (LV) relaxation observed in control infarcts acutely (24 h post-MI). At 8 weeks following treatment, CM therapy augmented LV contractility and relaxation, IZ angiogenesis and inhibited infarct size expansion, wall expansion, and wall thinning. All of these acute and chronic beneficial effects of CM therapy were vitiated by neutralizing antibodies to IGF-1 but not by control IgG. Moreover, the addition of neutralizing IGF-1 antibody to control medium had no effect on these structural or functional changes in the heart post-treatment.
Insulin-like growth factor-1 within the EPC CM mediates potent acute myocardial repair and chronic remodelling effects post-MI. These findings may provide a rationale for comparative trials of specific growth factors vs. current progenitor cell strategies.</description><subject>Animals</subject><subject>Antibodies, Neutralizing - physiology</subject><subject>Apoptosis - physiology</subject><subject>Biomarkers - metabolism</subject><subject>Cardiotonic Agents - pharmacology</subject><subject>Cell Survival</subject><subject>Culture Media, Conditioned - pharmacology</subject><subject>Endothelial Cells - physiology</subject><subject>Endothelial Cells - transplantation</subject><subject>Female</subject><subject>Heart Ventricles - pathology</subject><subject>Insulin-Like Growth Factor I - antagonists & inhibitors</subject><subject>Insulin-Like Growth Factor I - immunology</subject><subject>Insulin-Like Growth Factor I - pharmacology</subject><subject>Myocardial Contraction - physiology</subject><subject>Myocardial Infarction - metabolism</subject><subject>Myocardial Infarction - pathology</subject><subject>Myocardial Infarction - therapy</subject><subject>Myocytes, Cardiac - physiology</subject><subject>Neovascularization, Physiologic - physiology</subject><subject>Phosphorylation</subject><subject>Proto-Oncogene Proteins c-akt - metabolism</subject><subject>Stem Cell Transplantation - methods</subject><subject>Stem Cells - physiology</subject><subject>Sus scrofa</subject><subject>Ventricular Dysfunction, Left - pathology</subject><subject>Ventricular Dysfunction, Left - therapy</subject><issn>0195-668X</issn><issn>1522-9645</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9UUtv1DAQthAVXQp3TshHDpjacWwnR1SVh1QJDq3ELZo4441L1g62I7R_jt_WpFt6Go3me8zMR8g7wT8J3spLXNKIkMr9JY6pluoF2QlVVazVtXpJdly0imnd_Donr3O-55w3WuhX5LyqhJEtb3fk389YMBSKYYhlxMnDROcU9xh8iYlanCZmYxh88THgQA84eGAJJyhrB6F4BnOcSyzefqQW0uBjSXEetxbCsIkxCHv_KGkpOoe2ZDrHXNjhGB8Zq6cPDpLdTCgkPNlsDv1xHeVl8oFN_jfSfYp_y0gd2HU9Jt6QMwdTxrdP9YLcfbm-vfrGbn58_X71-YbZmpvCatDKDQjGgalEbRpurBC95n2rJIDhympRKy0tgOODVIBNLW3r-tZJ1Rh5QT6cdNdz_iyYS3fweXsOBIxL7oQUK9tUfIPyE9SmmHNC183JHyAdO8G7LbXuObXulNpKef-kvvTr5c-E_zHJB0_tnLM</recordid><startdate>20130301</startdate><enddate>20130301</enddate><creator>Hynes, Brian</creator><creator>Kumar, Arun H S</creator><creator>O'Sullivan, John</creator><creator>Klein Buneker, Chirlei</creator><creator>Leblond, Anne-Laure</creator><creator>Weiss, Sharon</creator><creator>Schmeckpeper, Jeffrey</creator><creator>Martin, Kenneth</creator><creator>Caplice, Noel M</creator><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>20130301</creationdate><title>Potent endothelial progenitor cell-conditioned media-related anti-apoptotic, cardiotrophic, and pro-angiogenic effects post-myocardial infarction are mediated by insulin-like growth factor-1</title><author>Hynes, Brian ; Kumar, Arun H S ; O'Sullivan, John ; Klein Buneker, Chirlei ; Leblond, Anne-Laure ; Weiss, Sharon ; Schmeckpeper, Jeffrey ; Martin, Kenneth ; Caplice, Noel M</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c407t-4a65fdea7fa72147807c11b60b953aa705c614563caaf0d35ae843c9fb9f35873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Animals</topic><topic>Antibodies, Neutralizing - physiology</topic><topic>Apoptosis - physiology</topic><topic>Biomarkers - metabolism</topic><topic>Cardiotonic Agents - pharmacology</topic><topic>Cell Survival</topic><topic>Culture Media, Conditioned - pharmacology</topic><topic>Endothelial Cells - physiology</topic><topic>Endothelial Cells - transplantation</topic><topic>Female</topic><topic>Heart Ventricles - pathology</topic><topic>Insulin-Like Growth Factor I - antagonists & inhibitors</topic><topic>Insulin-Like Growth Factor I - immunology</topic><topic>Insulin-Like Growth Factor I - pharmacology</topic><topic>Myocardial Contraction - physiology</topic><topic>Myocardial Infarction - metabolism</topic><topic>Myocardial Infarction - pathology</topic><topic>Myocardial Infarction - therapy</topic><topic>Myocytes, Cardiac - physiology</topic><topic>Neovascularization, Physiologic - physiology</topic><topic>Phosphorylation</topic><topic>Proto-Oncogene Proteins c-akt - metabolism</topic><topic>Stem Cell Transplantation - methods</topic><topic>Stem Cells - physiology</topic><topic>Sus scrofa</topic><topic>Ventricular Dysfunction, Left - pathology</topic><topic>Ventricular Dysfunction, Left - therapy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hynes, Brian</creatorcontrib><creatorcontrib>Kumar, Arun H S</creatorcontrib><creatorcontrib>O'Sullivan, John</creatorcontrib><creatorcontrib>Klein Buneker, Chirlei</creatorcontrib><creatorcontrib>Leblond, Anne-Laure</creatorcontrib><creatorcontrib>Weiss, Sharon</creatorcontrib><creatorcontrib>Schmeckpeper, Jeffrey</creatorcontrib><creatorcontrib>Martin, Kenneth</creatorcontrib><creatorcontrib>Caplice, Noel M</creatorcontrib><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>European heart journal</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hynes, Brian</au><au>Kumar, Arun H S</au><au>O'Sullivan, John</au><au>Klein Buneker, Chirlei</au><au>Leblond, Anne-Laure</au><au>Weiss, Sharon</au><au>Schmeckpeper, Jeffrey</au><au>Martin, Kenneth</au><au>Caplice, Noel M</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Potent endothelial progenitor cell-conditioned media-related anti-apoptotic, cardiotrophic, and pro-angiogenic effects post-myocardial infarction are mediated by insulin-like growth factor-1</atitle><jtitle>European heart journal</jtitle><addtitle>Eur Heart J</addtitle><date>2013-03-01</date><risdate>2013</risdate><volume>34</volume><issue>10</issue><spage>782</spage><epage>789</epage><pages>782-789</pages><issn>0195-668X</issn><eissn>1522-9645</eissn><abstract>We have previously reported the cardioprotective effects of endothelial progenitor cell (EPC)-conditioned media (CM) therapy post-myocardial infarction (MI). In the present study, we have determined the insulin-like growth factor-1 (IGF-1) contribution to EPC CM effects on cardiomyocyte survival, contractility, and angiogenesis in vivo.
Conditioned media from porcine EPC were administered intracoronary in the presence and absence of specific neutralizing antibodies to IGF-1 or control IgG in a porcine model of MI. X-vivo (non-conditioned) medium was used as a control. Functional, histological, and biochemical parameters were evaluated at 24 h and 8-week post-therapy. Conditioned media therapy significantly abrogated infarct zone (IZ) apoptosis, hypocontractility, and impaired left ventricular (LV) relaxation observed in control infarcts acutely (24 h post-MI). At 8 weeks following treatment, CM therapy augmented LV contractility and relaxation, IZ angiogenesis and inhibited infarct size expansion, wall expansion, and wall thinning. All of these acute and chronic beneficial effects of CM therapy were vitiated by neutralizing antibodies to IGF-1 but not by control IgG. Moreover, the addition of neutralizing IGF-1 antibody to control medium had no effect on these structural or functional changes in the heart post-treatment.
Insulin-like growth factor-1 within the EPC CM mediates potent acute myocardial repair and chronic remodelling effects post-MI. These findings may provide a rationale for comparative trials of specific growth factors vs. current progenitor cell strategies.</abstract><cop>England</cop><pmid>22173909</pmid><doi>10.1093/eurheartj/ehr435</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0195-668X |
ispartof | European heart journal, 2013-03, Vol.34 (10), p.782-789 |
issn | 0195-668X 1522-9645 |
language | eng |
recordid | cdi_proquest_miscellaneous_1315637207 |
source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
subjects | Animals Antibodies, Neutralizing - physiology Apoptosis - physiology Biomarkers - metabolism Cardiotonic Agents - pharmacology Cell Survival Culture Media, Conditioned - pharmacology Endothelial Cells - physiology Endothelial Cells - transplantation Female Heart Ventricles - pathology Insulin-Like Growth Factor I - antagonists & inhibitors Insulin-Like Growth Factor I - immunology Insulin-Like Growth Factor I - pharmacology Myocardial Contraction - physiology Myocardial Infarction - metabolism Myocardial Infarction - pathology Myocardial Infarction - therapy Myocytes, Cardiac - physiology Neovascularization, Physiologic - physiology Phosphorylation Proto-Oncogene Proteins c-akt - metabolism Stem Cell Transplantation - methods Stem Cells - physiology Sus scrofa Ventricular Dysfunction, Left - pathology Ventricular Dysfunction, Left - therapy |
title | Potent endothelial progenitor cell-conditioned media-related anti-apoptotic, cardiotrophic, and pro-angiogenic effects post-myocardial infarction are mediated by insulin-like growth factor-1 |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-13T14%3A45%3A47IST&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=Potent%20endothelial%20progenitor%20cell-conditioned%20media-related%20anti-apoptotic,%20cardiotrophic,%20and%20pro-angiogenic%20effects%20post-myocardial%20infarction%20are%20mediated%20by%20insulin-like%20growth%20factor-1&rft.jtitle=European%20heart%20journal&rft.au=Hynes,%20Brian&rft.date=2013-03-01&rft.volume=34&rft.issue=10&rft.spage=782&rft.epage=789&rft.pages=782-789&rft.issn=0195-668X&rft.eissn=1522-9645&rft_id=info:doi/10.1093/eurheartj/ehr435&rft_dat=%3Cproquest_cross%3E1315637207%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=1315637207&rft_id=info:pmid/22173909&rfr_iscdi=true |