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Author Notes:

Chunhui Xu, chunhui.xu@emory.edu

A.R., K.M., and C.X. designed experiments. A.R., P.F., D.L., H.H., L.C.A., and J.M. performed experiments and analyzed data. J.F. and G.B. contributed to the MVP hardware design and testing. A.R. and C.X. wrote the manuscript. All authors reviewed and approved the manuscript.

We thank Astronaut Jessica Meir and Astronaut Andrew Morgan for performing cell culture experiments aboard the ISS and Gregory Tharp and Kathryn Pellegrini at Emory University for RNA-seq analysis. We also thank Dr. Bill McLamb and Dr. Marc Giulianotti of the CASIS for guidance and discussions. The graphical abstract was created with BioRender.com. This study was supported in part by the Center for Advancement of Science in Space (GA-2017-266), the National Institutes of Health (R01HL136345 and R01AA028527), and the National Science Foundation and the Center for Advancement of Science in Space (CBET 1926387).

J.F. and G.B. were employees of Techshot. All other authors declare no competing interests.

Subjects:

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Cell & Tissue Engineering
  • Cell Biology
  • PLURIPOTENT STEM-CELLS
  • GROWING TISSUES
  • PROTEIN
  • DIFFERENTIATION
  • ANGIOPOIETIN-2
  • BIOREACTOR
  • MATURATION

Space microgravity improves proliferation of human iPSC-derived cardiomyocytes

Tools:

Journal Title:

STEM CELL REPORTS

Volume:

Volume 17, Number 10

Publisher:

, Pages 2272-2285

Type of Work:

Article | Final Publisher PDF

Abstract:

In microgravity, cells undergo profound changes in their properties. However, how human cardiac progenitors respond to space microgravity is unknown. In this study, we evaluated the effect of space microgravity on differentiation of human induced pluripotent stem cell (hiPSC)-derived cardiac progenitors compared with 1G cultures on the International Space Station (ISS). Cryopreserved 3D cardiac progenitors were cultured for 3 weeks on the ISS. Compared with 1G cultures, the microgravity cultures had 3-fold larger sphere sizes, 20-fold higher counts of nuclei, and increased expression of proliferation markers. Highly enriched cardiomyocytes generated in space microgravity showed improved Ca2+ handling and increased expression of contraction-associated genes. Short-term exposure (3 days) of cardiac progenitors to space microgravity upregulated genes involved in cell proliferation, survival, cardiac differentiation, and contraction, consistent with improved microgravity cultures at the late stage. These results indicate that space microgravity increased proliferation of hiPSC-cardiomyocytes, which had appropriate structure and function.

Copyright information:

© 2022 The Author(s)

This is an Open Access work distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/).
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