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dc.contributorNot Applicableen_US
dc.contributor.authorCANTY, JOHN M Principal Investigatoren_US
dc.date30-Nov-14en_US
dc.date2011en_US
dc.date.accessioned2011-04-18T21:03:45Zen_US
dc.date.accessioned2011-04-19T18:31:06Z
dc.date.available1-Aug-96en_US
dc.date.available2011-04-18T21:03:45Zen_US
dc.date.available2011-04-19T18:31:06Z
dc.date.issued2011-04-18T21:03:45Zen_US
dc.identifier8041339en_US
dc.identifier2R01HL055324-11en_US
dc.identifier55324en_US
dc.identifier.urihttp://hdl.handle.net/10477/1051
dc.descriptionAccounting;Address;adult stem cell;Anatomy;Animal Model;Apoptosis;Area;Autologous;base;Bioluminescence;Biopsy;Blood Vessels;Bone Marrow;Cardiac;Cardiac Myocytes;Cell Death;cell preparation;Cell Size;Cell Therapy;cell type;Cells;cellular imaging;Cessation of life;Chronic;Cicatrix;Clinical;comparative;Congestive Heart Failure;Coronary Arteriosclerosis;density;Depressed mood;Development;Disease;Drug Formulations;EFRAC;end stage disease;Family suidae;Fluorescence;Functional disorder;Growth Factor;Heart;heart dimension/size;Heart Diseases;Heart failure;Human;Image;Immunohistochemistry;improved;improved functioning;in vivo;Infarction;Injection of therapeutic agent;innovation;insight;Ischemia;Label;Lead;Left;Left Ventricular Mass;Left Ventricular Remodeling;liquid chromatography mass spectrometry;Mass Spectrum Analysis;Mesenchymal;Mesenchymal Stem Cells;Modeling;Muscle Cells;Myocardial;Myocardial Infarction;Myocardial Ischemia;Myocardial perfusion;Myocardial Reperfusion;Myocardium;Natural regeneration;novel strategies;Nuclear;paracrine;Patients;Perfusion;PET/CT scan;Phenotype;Physiological;preclinical study;Prevalence;prevent;Prevention strategy;Proliferating;Proteins;Proteomics;public health relevance;Relative (related person);release factor;repaired;Reperfusion Therapy;Reporter;Rest;Role;Source;Staging;stem cell differentiation;stem cell fate;stem cell therapy;Stem cells;stressor;success;Therapeutic Intervention;Time;Tissue Sample;Tissues;Translations;Vasodilation;Ventricular;Work;en_US
dc.descriptionAmount: $ 442419en_US
dc.description.abstractDESCRIPTION (provided by applicant): While symptomatic congestive heart failure from coronary artery disease is increasing in prevalence, there are even more patients that have asymptomatic left ventricular systolic dysfunction (LVSD). Asymptomatic LVSD (or Stage B heart failure) accounts for the majority of patients with a depressed ejection fraction and coronary artery disease. Some of these patients have prior myocardial infarctions and nontransmural scars from the contemporary management of ST elevation MI with reperfusion therapy. Others have viable dysfunctional myocardium reflecting the slow but cumulative myocyte loss from repetitive ischemia and left ventricular remodeling. This proposal is intended to determine whether intracoronary cell based therapy can ameliorate regional LV dysfunction at a stage of disease where clinical heart failure is absent and ongoing myocyte death and neurohormonal activation are minimal. The central hypothesis is that a myocardial microenvironment devoid of ongoing stressors promoting cell death will facilitate exogenous and endogenous myocyte regeneration from cell based therapy. Our completed work in a model of hibernating myocardium devoid of infarction supports this hypothesis and demonstrates that intracoronary mesenchymal stem cells (icMSCs) stimulate endogenous myocyte proliferation through a paracrine mechanism with a resultant increase in myocyte nuclear density. Cardiosphere derived cells (CDCs) isolated from myocardial biopsies provide an alternative source of adult stem cells that have been demonstrated to improve function after intracoronary injection through both direct differentiation into cardiac myocytes as well as by stimulating endogenous myocyte proliferation. In a head-to-head fashion, this proposal will determine the relative efficacy of these two therapies in viable dysfunctional myocardium vs. reperfused myocardial infarcts prior to the development of heart failure. To ultimately enhance translation, studies will be conducted in swine with a heart size similar to humans. Aim 1 will determine whether icCDCs are superior to icMSCs in chronic regional LV dysfunction. They will also define whether treatments are more efficacious when administered to hibernating vs. infarcted myocardium. Physiological end-points will include improvement in regional LV function and myocardial perfusion at rest and vasodilation. Aim 2 will evaluate the role of icMSCs and CDCs to amplify endogenous myocyte proliferation vs. differentiation of stem cells into a cardiac phenotype. Serial stem cell fate will be tracked in vivo using PET/CT 18[F]FHBG imaging of cells transfected with a lentiviral triple reporter construct complimented with fluorescence and bioluminescence in tissue samples. Serial assessment of LV mass, volumes and infarct size from imaging will be complimented with immunohistochemistry to quantify the amount of new myocardium regenerated. Aim 3 will use a discovery based proteomic approach employing label free LC/MS to identify paracrine factors differentially upregulated following icCDCs and icMSCs. The results will identify the stem cell and pathological substrate most likely to benefit patients with asymptomatic LVSD before clinical heart failure develops. PUBLIC HEALTH RELEVANCE: This project is highly relevant to the contemporary management of the vast majority of patients following reperfused myocardial infarction as well as chronic coronary artery disease where LV systolic function is mildly depressed without symptomatic heart failure. Demonstrating a beneficial effect of stem cell therapies on myocardial regeneration could change our current treatment paradigm which focuses on advanced end-stage disease to one that employs cell based therapy to prevent the progression of asymptomatic LV systolic dysfunction to clinical heart failure.en_US
dc.titleCHRONIC ADAPTATIONS TO MYOCARDIAL ISCHEMIAen_US
dc.typeNIH Grant Awarden_US


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