Stemness and Differentiation Potential Are Defined by Metabolism in Cardiac Progenitor Cells The limited capacity for regeneration in the adult mammalian heart can be augmented by c-Kit+ cardiac progenitor cells (CPCs). However, reparative potential of CPCs is compromised by genetic and environmental factors including aging and pathological injury. Similarly, genetic and environmental factors influence the metabolic profile and mitochondrial function of CPCs isolated from adult human heart tissue. Moreover, isolation and expansion of CPCs activates metabolic pathways that are dormant in quiescent cells. Several studies have established a link between metabolism and stem cell phenotypic characteristics of pluripotency, commitment, and viability. For example, glycolysis supports rapid cell proliferation while minimizing the production of damaging reactive oxygen species. In contrast, mitochondrial respiration is essential for differentiation, but oxidative metabolism depletes the stem cell pool and accelerates cellular senescence. The hypothesis of this project is that metabolism and stemness of human CPCs are interrelated such that CPC stemness is dependent on a glycolytic phenotype and differentiation requires biogenesis of mitochondria for oxidative metabolism. To address this hypothesis, two specific aims are proposed: (1) Metabolism regulates CPC biology: glycolysis augments proliferation and delays senescence, while oxidative phosphorylation enhances lineage commitment; and (2) Predisposition to lineage commitment can be augmented by increasing mitochondrial function. The significance of this research lies in applying findings to predict CPC function derived from patient samples to optimize regenerative treatment for individuals based on stem cell metabolic phenotype. The short-term goal of the project is to optimize in vitro expansion and lineage commitment of human CPCs by modulating metabolism. The long-term goal is the identification of drug-targetable regulators of metabolism to improve the regenerative capacity of CPCs in patients. The novelty of this research rests in elucidating relationships between metabolism, self-renewal and lineage commitment in human CPCs. The impact of this research will be to reveal how stress conditions and changes in microenvironment affect the metabolic phenotype of cardiac stem cells, thereby establishing new interventional approaches and potentiate the likelihood of success for CPC-based interventional therapies.

Public Health Relevance

Cardiac progenitor cells isolated from human patients for autologous transplantation show therapeutic potential in clinical trials but are of variable quality due to variability in patient health, history, and genetics. Enhancing the stem-cell like qualities of human CPCs may improve the health, viability, differentiation potential, and translational efficacy of these cells. I propose to investigate how human CPCs isolated from patients with cardiac defects can be altered by manipulation of their metabolic state, which will improve our understanding of CPC biology and yield potential techniques to improve the quality of CPCs for eventual use in autologous transplantation.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Postdoctoral Individual National Research Service Award (F32)
Project #
5F32HL136064-02
Application #
9424418
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Wang, Wayne C
Project Start
2017-02-01
Project End
2020-01-31
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
Kubli, Dieter A; Sussman, Mark A (2017) Eat, breathe, ROS: controlling stem cell fate through metabolism. Expert Rev Cardiovasc Ther 15:345-356
Sacchi, Veronica; Wang, Bingyan J; Kubli, Dieter et al. (2017) Peptidyl-Prolyl Isomerase 1 Regulates Ca2+ Handling by Modulating Sarco(Endo)Plasmic Reticulum Calcium ATPase and Na2+/Ca2+ Exchanger 1 Protein Levels and Function. J Am Heart Assoc 6: