A Mount Sinai-led team has developed a reproducible and scalable method to advance maturation of human pluripotent stem cell-derived cardiomyocytes (hPSC-CMs)—cells that support heart muscle contraction, generated in the lab from human stem cell lines—which researchers say will improve approaches for disease modeling, regenerative therapies, and drug testing. A study reporting this new protocol was published in the April 7 print edition of the journal Cell Stem Cell.
Mount Sinai researchers investigated multiple metabolic modifications in hPSC-CMs. The research team also identified the role of the protein known as peroxisome proliferator activated receptor delta (PPARd) in inducing what is referred to as the metabolic switch in the lab-generated heart muscle cells. This metabolic switch is a critical part of the maturation process of the heart.
“This work will create exciting opportunities to further assess human heart biology through multi-disciplinary approaches incorporating developmental biology, transcriptomics, contractile measurements and drug testing,” said senior author Nicole C. Dubois, PhD, Associate Professor of Cell, Developmental and Regenerative Biology at the Black Family Stem Cell Institute and The Mindich Child Health and Development Institute at the Icahn School of Medicine at Mount Sinai. “Our findings provide a new avenue to generate mature hPSC-CMs for disease modeling and regenerative therapy. We are moving a step closer to understanding how to leverage our knowledge of human development to improved access to mature human cell types.”
In the study, the researchers activated different signaling pathways in vitro to replicate the metabolic changes that would occur during heart development in the organism. They found that PPARd induces the metabolic switch from glycolysis to fatty acid oxidation in the lab setting, thus influencing whether heart muscle cells generate energy from glucose or fatty acids. While the signaling effects of the protein peroxisome proliferator activated receptor alpha (PPARa) are the most active in heart muscle cells, the researchers said PPARd signaling has a separate and important role in efficiently activating the gene regulatory networks, increasing the quantity and organization of the organelles involved in energy production, and augmenting the fatty acid oxidation process. The activation of signaling regulated by PPARd can further enhance heart muscle cell size and organization, and improve contractility, all hallmarks of heart maturation.
The research team also investigated the effects of lactate exposure, where heart muscle cells are able to survive on lactate in the absence of glucose. This is frequently used to enrich hPSC-CMs. The researchers found that this method can induce an independent mechanism of cardiac maturation, and when combined with PPARd, it enhances oxidative metabolism, allowing for efficient energy generation from both carbohydrates and fatty acids. This study allowed for a detailed analysis into the long-term effects of a commonly used protocol in the heart muscle field.
In collaboration with the Ma’ayan lab at Mount Sinai, the group has generated a comprehensive and publicly accessible dataset which details the transcriptomic changes observed by the Mount Sinai-led team. This dataset allows researchers studying either PPAR-regulated signaling or lactate selection to rapidly assess future targets for research or drug testing.
Mount Sinai’s Department of Pharmacological Sciences; The Friedman Brain Institute; the Departments of Psychiatry, Oncological Sciences, and Genetics and Genomic Sciences; the Institute for Systems Biomedicine; and the Department of Obstetrics and Gynecology contributed to this research, in addition to the Children’s Hospital of Philadelphia Research Institute and the University Medical Center Hamburg-Eppendorf.
This work was supported by funding from The Mindich Child Health and Development Institute and grants R01HL134956 and R56HL128646 from the National Institute of Health (NIH)/the National Heart, Lung, and Blood Institute (NHLBI).
About the Mount Sinai Health System
The Mount Sinai Health System is New York City’s largest academic medical system, encompassing eight hospitals, a leading medical school, and a vast network of ambulatory practices throughout the greater New York region. Mount Sinai advances medicine and health through unrivaled education and translational research and discovery to deliver care that is the safest, highest-quality, most accessible and equitable, and the best value of any health system in the nation. The Health System includes approximately 7,300 primary and specialty care physicians; 13 joint-venture ambulatory surgery centers; more than 415 ambulatory practices throughout the five boroughs of New York City, Westchester, Long Island, and Florida; and more than 30 affiliated community health centers. The Mount Sinai Hospital is ranked on U.S. News & World Report’s “Honor Roll” of the top 20 U.S. hospitals and is top in the nation by specialty: No. 1 in Geriatrics and top 20 in Cardiology/Heart Surgery, Diabetes/Endocrinology, Gastroenterology/GI Surgery, Neurology/Neurosurgery, Orthopedics, Pulmonology/Lung Surgery, Rehabilitation, and Urology. New York Eye and Ear Infirmary of Mount Sinai is ranked No. 12 in Ophthalmology. Mount Sinai Kravis Children's Hospital is ranked in U.S. News & World Report’s “Best Children’s Hospitals” among the country’s best in four out of 10 pediatric specialties. The Icahn School of Medicine is one of three medical schools that have earned distinction by multiple indicators: ranked in the top 20 by U.S. News & World Report’s “Best Medical Schools,” aligned with a U.S. News & World Report “Honor Roll” Hospital, and No. 14 in the nation for National Institutes of Health funding. Newsweek’s “The World’s Best Smart Hospitals” ranks The Mount Sinai Hospital as No. 1 in New York and in the top five globally, and Mount Sinai Morningside in the top 20 globally.
Cell Stem Cell
PPARdelta activation induces metabolic and contractile maturation of human pluripotent stem-cell-derived cardiomyocytes
Article Publication Date