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Fabrication of 3D Cardiac Microtissue Arrays using Human iPSC-Derived Cardiomyocytes, Cardiac Fibroblasts, and Endothelial Cells
Published on: March 14, 2021
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Space microgravity improves proliferation of human iPSC-derived cardiomyocytes
Antonio Rampoldi1, Parvin Forghani1, Dong Li1
1Department of Pediatrics, Emory University School of Medicine and Children's Healthcare of Atlanta, Atlanta, GA, USA.
Stem Cell Reports
|September 9, 2022
Summary
Space microgravity enhances human cardiac progenitor cell proliferation and differentiation. These cells, cultured on the International Space Station, showed improved function and structure, indicating potential for cardiac research in space.
Area of Science:
- Space biology
- Cardiovascular research
- Stem cell science
Background:
- Cellular properties change significantly in microgravity.
- The response of human cardiac progenitors to space microgravity is not well understood.
Purpose of the Study:
- To investigate the effect of space microgravity on the differentiation of human induced pluripotent stem cell (hiPSC)-derived cardiac progenitors.
- To compare microgravity cultures with 1G cultures on the International Space Station (ISS).
Main Methods:
- Cryopreserved 3D cardiac progenitors were cultured for 3 weeks on the ISS.
- Comparison of microgravity cultures with 1G controls.
Main Results:
- Microgravity cultures exhibited 3-fold larger sphere sizes and 20-fold higher nuclei counts compared to 1G.
- Increased expression of proliferation markers was observed in microgravity.
- Cardiomyocytes generated in microgravity showed improved Ca2+ handling and increased expression of contraction-associated genes.
- Short-term (3-day) microgravity exposure upregulated genes related to proliferation, survival, cardiac differentiation, and contraction.
Conclusions:
- Space microgravity promotes the proliferation of hiPSC-cardiomyocytes.
- Microgravity-generated hiPSC-cardiomyocytes possess appropriate structure and function.
- Findings suggest microgravity conditions can enhance cardiac progenitor cell development for research applications.
Keywords:
calcium handlingcardiac progenitorscardiomyocytesdifferentiationfunctiongene experssisonhuman induced pluripotent stem cellsmicrogravityproliferationspaceflight
