Award Abstract # 1926387
ISS: Engineering Stem Cell-Derived Cardiac Microtissues with Metabolic Regulators in Space to Promote Cardiomyocyte Maturation

NSF Org: CBET
Division of Chemical, Bioengineering, Environmental, and Transport Systems
Recipient: EMORY UNIVERSITY
Initial Amendment Date: July 8, 2019
Latest Amendment Date: April 1, 2024
Award Number: 1926387
Award Instrument: Standard Grant
Program Manager: Rizia Bardhan
rbardhan@nsf.gov
 (703)292-2390
CBET
 Division of Chemical, Bioengineering, Environmental, and Transport Systems
ENG
 Directorate for Engineering
Start Date: September 1, 2019
End Date: August 31, 2024 (Estimated)
Total Intended Award Amount: $399,999.00
Total Awarded Amount to Date: $476,990.00
Funds Obligated to Date: FY 2019 = $399,999.00
FY 2024 = $76,991.00
History of Investigator:
  • Chunhui Xu (Principal Investigator)
    chunhui.xu@emory.edu
Recipient Sponsored Research Office: Emory University
201 DOWMAN DR NE
ATLANTA
GA  US  30322-1061
(404)727-2503
Sponsor Congressional District: 05
Primary Place of Performance: Emory University
2015 Uppergate Drive
Atlanta
GA  US  30322-1014
Primary Place of Performance
Congressional District:
05
Unique Entity Identifier (UEI): S352L5PJLMP8
Parent UEI:
NSF Program(s): Cellular & Biochem Engineering,
Engineering of Biomed Systems
Primary Program Source: 01002425DB NSF RESEARCH & RELATED ACTIVIT
01001920DB NSF RESEARCH & RELATED ACTIVIT
Program Reference Code(s): 070Z
Program Element Code(s): 149100, 534500
Award Agency Code: 4900
Fund Agency Code: 4900
Assistance Listing Number(s): 47.041

ABSTRACT

Cardiac muscle cells generated from stem cells could be used to replace damaged cells in patients with heart disease, which is the leading cause of death in the United States. Scientists have also used these cells to study heart disease and drug responses. Currently, when scientists grow cardiac muscle cells in a dish, the characteristics of these cells look like the heart cells at the early developmental stage; their shape, size, and function resemble immature heart cells. Ideally, more mature cardiac muscle cells are needed in cardiac cell replacement therapy and the study of heart disease. Therefore, developing methods to accelerate the maturation of cardiac muscle cells is highly significant. The unique environment of the International Space Station (ISS) is known to provide beneficial effects on human cardiac precursors to help their growth and differentiation. In this project, the research team will investigate the maturation of stem cell-derived cardiac muscle cells by growing these cells in tissue-like structures in the ISS. The investigators also plan to develop a technology to promote cardiac muscle cell maturation in microtissues that are suitable for large-scale production, a requirement essential for translational research. This project also incorporates the training of young scientists and students and provides science-learning opportunities for kids in a local hospital in the Children's Healthcare of Atlanta system.

The goal of this project is to establish a multipronged approach combining microgravity, tissue engineering and metabolic regulation to promote the maturation of cardiomyocytes derived from human induced pluripotent stem cells (hiPSC-CMs). First, the investigators will optimize the design of tissue engineering and cell culture conditions in ground-based experiments by examining the effect of simulated microgravity, cell composition and metabolic regulation. Second, the hiPSC-CM microtissues will be cultured in the ISS. The experiments will be performed within a perfusion system that is suitable for suspension cell culture and has gas permeable membranes that allow sufficient gas exchange for cell growth. The cells will remain in the same culture units throughout the experiment and cell morphology will be monitored once a week utilizing an inverted phasecontrast microscope currently available at the ISS, and the imaging data will be transmitted for ground-based control and data retrieval. Following spaceflight, the researchers will investigate molecular and functional characteristics of the hiPSC-CMs. Exposure of hiPSC-CM microtissues to microgravity in space is expected to eliminate shear stress and consequently enhance cell-cell and cell-matrix interactions within multicellular architectures. Findings from this project will provide insights into the molecular regulation of accelerated hiPSC-CM maturation. Applying these insights to the research on earth could assist in the production of more mature hiPSC-CMs to enhance their potential application in regenerative medicine, the study of heart disease and drug development. (Project integration and operation on the ISS will be provided by the Center for the Advancement of Science in Space (CASIS) implementation partner, BioServe.)

This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.

PUBLICATIONS PRODUCED AS A RESULT OF THIS RESEARCH

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Forghani P, Rashid A "Carfilzomib Treatment Causes Molecular and Functional Alterations of Human Induced Pluripotent Stem Cell-Derived Cardiomyocytes" Journal of the American Heart Association , v.7 , 2021 https://doi.org/10.1161/JAHA.121.022247 Citation Details
Hwang H, Liu R "Machine learning identifies abnormal Ca 2+ transients in human induced pluripotent stem cell-derived cardiomyocytes" Scientific reports , 2020 Citation Details
Hwang, Hyun and Liu, Rui and Eldridge, Ronald and Hu, Xin and Forghani, Parvin and Jones, Dean P. and Xu, Chunhui "Chronic ethanol exposure induces mitochondrial dysfunction and alters gene expression and metabolism in human cardiac spheroids" Alcohol: Clinical and Experimental Research , v.47 , 2023 https://doi.org/10.1111/acer.15026 Citation Details
Hwang, Hyun and Liu, Rui and Maxwell, Joshua T. and Yang, Jingjing and Xu, Chunhui "Machine learning identifies abnormal Ca2+ transients in human induced pluripotent stem cell-derived cardiomyocytes" Scientific Reports , v.10 , 2020 https://doi.org/10.1038/s41598-020-73801-x Citation Details
Hwang, Hyun and Rampoldi, Antonio and Forghani, Parvin and Li, Dong and Fite, Jordan and Boland, Gene and Maher, Kevin and Xu, Chunhui "Space microgravity increases expression of genes associated with proliferation and differentiation in human cardiac spheres" npj Microgravity , v.9 , 2023 https://doi.org/10.1038/s41526-023-00336-6 Citation Details
Li, Dong and Armand, Lawrence C. and Sun, Fangxu and Hwang, Hyun and Wolfson, David and Rampoldi, Antonio and Liu, Rui and Forghani, Parvin and Hu, Xin and Yu, Wen-Mei and Qu, Cheng-Kui and Jones, Dean P. and Wu, Ronghu and Cho, Hee Cheol and Maxwell, Jos "AMPK activator-treated human cardiac spheres enhance maturation and enable pathological modeling" Stem Cell Research & Therapy , v.14 , 2023 https://doi.org/10.1186/s13287-023-03554-7 Citation Details
Liu, Rui and Sun, Fangxu and Armand, Lawrence C. and Wu, Ronghu and Xu, Chunhui "Chronic Ethanol Exposure Induces Deleterious Changes in Cardiomyocytes Derived from Human Induced Pluripotent Stem Cells" Stem Cell Reviews and Reports , v.17 , 2021 https://doi.org/10.1007/s12015-021-10267-y Citation Details
Liu, Rui and Sun, Fangxu and Forghani, Parvin and Armand, Lawrence C. and Rampoldi, Antonio and Li, Dong and Wu, Ronghu and Xu, Chunhui "Proteomic Profiling Reveals Roles of Stress Response, Ca 2+ Transient Dysregulation, and Novel Signaling Pathways in AlcoholInduced Cardiotoxicity" Alcoholism: Clinical and Experimental Research , v.44 , 2020 https://doi.org/10.1111/acer.14471 Citation Details
Rampoldi, Antonio and Forghani, Parvin and Li, Dong and Hwang, Hyun and Armand, Lawrence Christian and Fite, Jordan and Boland, Gene and Maxwell, Joshua and Maher, Kevin and Xu, Chunhui "Space microgravity improves proliferation of human iPSC-derived cardiomyocytes" Stem Cell Reports , v.17 , 2022 https://doi.org/10.1016/j.stemcr.2022.08.007 Citation Details

PROJECT OUTCOMES REPORT

Disclaimer

This Project Outcomes Report for the General Public is displayed verbatim as submitted by the Principal Investigator (PI) for this award. Any opinions, findings, and conclusions or recommendations expressed in this Report are those of the PI and do not necessarily reflect the views of the National Science Foundation; NSF has not approved or endorsed its content.

The ability to produce heart muscle cells from human stem cells holds great potential for clinical application to replace damaged cells in patients with heart disease, the leading cause of death in the United States. However, these heart cells behave like the cells at the early developmental stage and remain immature. Transplantation of immature heart cells may result in complications such as irregular heartbeats. In addition, cell replacement therapy faces challenges in cell survival upon transplantation. Therefore, developing new strategies to accelerate heart cell maturation and improve cell survival is highly significant.

 

The unique environment of the International Space Station (ISS) can have profound effects on cell characteristics. This project investigated the impact of microgravity on heart muscle cells. We first generated heart microtissues from stem cells and initially examined how cells responded to simulated microgravity using a device before we conducted the experiment on the ISS. We found that simulated microgravity improved the maturation of heart cells. We then sent the heart microtissues to the ISS through SpaceX Crew-8 mission. Astronauts successfully conducted the experiment and sent beating heart cells back to Earth for further analyses. We found that a short duration of space microgravity increased levels of molecules related to cell survival and metabolism, features with the potential to improve the use of the cells for cell therapy. During this project, we published research findings in 9 research articles. Findings from this project will provide insights into improving the production of high-quality heart cells for the treatment of heart disease. This project has also incorporated the research training for young scientists and students and provided learning opportunities for general audiences.


Last Modified: 11/12/2024
Modified by: Chunhui Xu

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