TY - JOUR
T1 - 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
AU - Hynes, Brian
AU - Kumar, Arun H.S.
AU - O'Sullivan, John
AU - Klein Buneker, Chirlei
AU - Leblond, Anne Laure
AU - Weiss, Sharon
AU - Schmeckpeper, Jeffrey
AU - Martin, Kenneth
AU - Caplice, Noel M.
N1 - Funding Information:
This work was supported by grants from Science Foundation Ireland, Dublin, Ireland (R11482 and RFP06 to N.M.C.), Irish Heart Foundation, Dublin, Ireland (R12348 to B.H. and A.H.S.K.), and Molecular Medicine Ireland, Dublin, Ireland (R12699 to J.O.S.).
PY - 2013/3
Y1 - 2013/3
N2 - AimsWe 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.Methods and resultsConditioned 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.ConclusionInsulin- 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. All rights reserved.
AB - AimsWe 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.Methods and resultsConditioned 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.ConclusionInsulin- 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. All rights reserved.
KW - Conditioned media
KW - Insulin-like growth factor-1
KW - Myocardial infarction
KW - Porcine endothelial progenitor cell
UR - http://www.scopus.com/inward/record.url?scp=84874833681&partnerID=8YFLogxK
U2 - 10.1093/eurheartj/ehr435
DO - 10.1093/eurheartj/ehr435
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C2 - 22173909
AN - SCOPUS:84874833681
SN - 0195-668X
VL - 34
SP - 782
EP - 789
JO - European Heart Journal
JF - European Heart Journal
IS - 10
ER -