Project 3: Translational Model of Cell-Based Therapy for Myocardial Infarction. Project 3 proposes to develop and test in vivo, cell-based therapies to improve cardiac function following infarction. Two therapeutic approaches will be studied: 1) Injection of immortalized, clonal populations of marrow stromal cells (MSC), or their secreted products, to facilitate endogenous recovery. 2) Engraftment of exogenous cardiomyocytes (CMs), with/without MSC or MSC-derived factors. The exogenous CMs will be harvested from prenatal hearts or differentiated from either embryonic stem cells (ESC) or induced pluripotent stem cells (iPSC). These studies will be performed first in a rat model, which is well developed by investigators in this program, and allows for a sufficiently large number of animals to test several variables. Once a beneficial protocol is identified in the rat model it will be applied to the canine model. Torok-Storb and colleagues have extensive experience with cell transplantation in the dog model. In particular the issues of allograft rejection and the benefits and consequences of immunosuppression accurately reflect these same complications in patients, therefore strategies to address these issues will be clinically relevant. This stepwise plan, from rats to dogs, will limit the number of dogs required. There are three specific aims to address these goals.
Aim 1 proposes to generate and characterize cardiomyocytes (CM) derived from canine embryonic stem cells (ESC) and from induced pluripotent stem cells (iPSC).
Aim 2 will test the hypothesis that MSC facilitate endogenous repair and revascularization, induce tolerance, and promote engraftment of cardiomyocytes in the rat model. For this purpose immortalized and cloned MSC lines have been generated to provide reagents that can be well characterized and provide a consistent product for investigation. Dog MSC lines functionally analogous to rat MSC lines will be identified and used in Aim 3 to repair an infarcted heart in the dog model. These studies will serve to establish a robust large animal model for developing protocols and testing the efficacy and safety of cell based therapies for treating myocardial infarcts.

Public Health Relevance

The proposed studies in this project will serve to establish a robust large animal model for developing protocols and testing the long-term efficacy and safety of cell based therapies for treating myocardial infarcts.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL094374-05
Application #
8676869
Study Section
Heart, Lung, and Blood Initial Review Group (HLBP)
Project Start
Project End
Budget Start
2014-06-01
Budget End
2015-05-31
Support Year
5
Fiscal Year
2014
Total Cost
$293,833
Indirect Cost
$53,949
Name
University of Washington
Department
Type
DUNS #
605799469
City
Seattle
State
WA
Country
United States
Zip Code
98195
Liu, Yen-Wen; Chen, Billy; Yang, Xiulan et al. (2018) Human embryonic stem cell-derived cardiomyocytes restore function in infarcted hearts of non-human primates. Nat Biotechnol 36:597-605
Hofsteen, Peter; Robitaille, Aaron Mark; Strash, Nicholas et al. (2018) ALPK2 Promotes Cardiogenesis in Zebrafish and Human Pluripotent Stem Cells. iScience 2:88-100
Neidig, Lauren E; Weinberger, Florian; Palpant, Nathan J et al. (2018) Evidence for Minimal Cardiogenic Potential of Stem Cell Antigen 1-Positive Cells in the Adult Mouse Heart. Circulation 138:2960-2962
Leonard, Andrea; Bertero, Alessandro; Powers, Joseph D et al. (2018) Afterload promotes maturation of human induced pluripotent stem cell derived cardiomyocytes in engineered heart tissues. J Mol Cell Cardiol 118:147-158
Hansen, Katrina J; Laflamme, Michael A; Gaudette, Glenn R (2018) Development of a Contractile Cardiac Fiber From Pluripotent Stem Cell Derived Cardiomyocytes. Front Cardiovasc Med 5:52
Eschenhagen, Thomas; Bolli, Roberto; Braun, Thomas et al. (2017) Cardiomyocyte Regeneration: A Consensus Statement. Circulation 136:680-686
Hansen, Katrina J; Favreau, John T; Gershlak, Joshua R et al. (2017) Optical Method to Quantify Mechanical Contraction and Calcium Transients of Human Pluripotent Stem Cell-Derived Cardiomyocytes. Tissue Eng Part C Methods 23:445-454
Palpant, Nathan J; Wang, Yuliang; Hadland, Brandon et al. (2017) Chromatin and Transcriptional Analysis of Mesoderm Progenitor Cells Identifies HOPX as a Regulator of Primitive Hematopoiesis. Cell Rep 20:1597-1608
Palpant, Nathan J; Pabon, Lil; Friedman, Clayton E et al. (2017) Generating high-purity cardiac and endothelial derivatives from patterned mesoderm using human pluripotent stem cells. Nat Protoc 12:15-31
Yang, Xiulan; Murry, Charles E (2017) One Stride Forward: Maturation and Scalable Production of Engineered Human Myocardium. Circulation 135:1848-1850

Showing the most recent 10 out of 93 publications