Stem cell mediated cardiac repair is an exciting and controversial area of cardiovascular research that holds the potential to produce novel, revolutionary therapies for the treatment of heart disease. Extensive investigation to define cell types contributing to cardiac formation, homeostasis and regeneration has produced several candidates, including adult cardiac c-Kit+ expressing stem and progenitor cells that have even been employed in a Phase I clinical trial demonstrating beneficial outcome for many patients together with safety and feasibility of this therapeutic approach. Despite many promising studies including the SCIPIO clinical trial, the significance of the c-kit+ cell population in cardiac regeneration is persistently debated among many cardiovascular researchers and clinicians. Therefore, further investigation conducted with rigorous experimental design, methodology, and interpretation is essential to resolve current ambiguities and advance the field of cardiac regenerative therapy. In that spirit, this proposal determines the role of c-Kit+ cell participation in cardiac repair using a novel, inducible transgenic mouse model to genetically tag c-Kit expressing cells during development, following injury and in the aging heart. In contrast to ?knock-in? approaches employed in many recent c-Kit lineage-tracing models that generate a hemizygous genotype for endogenous c-Kit, the strategy proposed here exploits overexpression of a validated exogenous c-Kit promoter construct to drive expression of the rtTA transactivator. This construct in combination with promoters regulated by the tetracycline responsive element (TRE) induces transcription of the TRE controlled reporter upon administration of doxycycline. c-Kit+ cells are tagged in a time-dependent manner transiently or permanently, depending upon the TRE controlled partner. Preliminary results show that c-Kit cells comprise a more diverse population than previously assumed, necessitating a more nuanced understanding of fundamental c-Kit biology and expression patterns.
Specific Aims are: 1) c-Kit+ stem cells contribute to adult cardiac tissue during tissue homeostasis and repair as demonstrated using genetic models for lineage tracing in vivo, 2) c-Kit+ cells contribute to cardiac formation during development and 3) c-Kit+ cells contribute to homeostasis in the aging heart. The innovation of this proposal is in the approach used to tag and track c-Kit cells such that endogenous c-Kit biology remains intact while overexpression confers greater sensitivity and therefore more extensive labeling of the c-Kit cell population. The significance of these studies is to clarify existing unresolved controversies in the field by establishing c-Kit cell expression and participation in cardiac formation and repair. Collectively, these studies will contribute essential information defining the importance of c-Kit+ cardiac progenitor populations as reagents for cell based therapy in the treatment of heart disease.

Public Health Relevance

Adult cardiac stem cells hold great promise for the treatment of heart disease. However, the field of cardiac cell based therapy remains deeply divided due to strong disagreement among researchers and clinicians over which cell types, if any, are the best candidates for these applications. Research models that identify and define specific cardiac cells that effectively contribute to heart repair are urgently needed to resolve this debate. The studies proposed here fulfill this requirement by providing novel animal models designed to track the behavior of c-Kit expressing cells during heart formation, after injury and in the aging heart. These findings will clarify which cells are the optimal candidates for cell based cardiac therapy to advance clinical treatment of heart failure.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Project (R01)
Project #
5R01HL135661-02
Application #
9413369
Study Section
Myocardial Ischemia and Metabolism Study Section (MIM)
Program Officer
Wong, Renee P
Project Start
2017-02-01
Project End
2021-01-31
Budget Start
2018-02-01
Budget End
2019-01-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
San Diego State University
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
073371346
City
San Diego
State
CA
Country
United States
Zip Code
92182
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Monsanto, Megan M; White, Kevin S; Kim, Taeyong et al. (2017) Concurrent Isolation of 3 Distinct Cardiac Stem Cell Populations From a Single Human Heart Biopsy. Circ Res 121:113-124
Monsanto, Megan M; Wang, Bingyan J; Sussman, Mark A (2017) Synthetic MSC? Nothing Beats the Real Thing. Circ Res 120:1694-1695