Space microgravity improves proliferation of human iPSC-derived cardiomyocytes

被引:20
|
作者
Rampoldi, Antonio [1 ,2 ]
Forghani, Parvin [1 ,2 ]
Li, Dong [1 ,2 ]
Hwang, Hyun [1 ,2 ]
Armand, Lawrence Christian [1 ,2 ]
Fite, Jordan [3 ]
Boland, Gene [3 ]
Maxwell, Joshua [1 ,2 ]
Maher, Kevin [1 ,2 ]
Xu, Chunhui [1 ,2 ,4 ,5 ]
机构
[1] Emory Univ, Dept Pediat, Sch Med, Atlanta, GA 30322 USA
[2] Emory Univ, Childrens Healthcare Atlanta, Atlanta, GA 30322 USA
[3] Techshot Inc, Greenville, IN USA
[4] Georgia Inst Technol, Wallace H Coulter Dept Biomed Engn, Atlanta, GA 30318 USA
[5] Emory Univ, Atlanta, GA 30318 USA
来源
STEM CELL REPORTS | 2022年 / 17卷 / 10期
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
PLURIPOTENT STEM-CELLS; GROWING TISSUES; PROTEIN; DIFFERENTIATION; ANGIOPOIETIN-2; BIOREACTOR; MATURATION;
D O I
10.1016/j.stemcr.2022.08.007
中图分类号
Q813 [细胞工程];
学科分类号
摘要
In microgravity, cells undergo profound changes in their properties. However, how human cardiac progenitors respond to space micro -gravity 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 pro-genitors 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 micro -gravity showed improved Ca2+ handling and increased expression of contraction-associated genes. Short-term exposure (3 days) of car-diac 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.
引用
收藏
页码:2272 / 2285
页数:14
相关论文
共 50 条
  • [31] Industrialized Production of Human iPSC-Derived Cardiomyocytes for Use in Drug Discovery and Toxicity Testing
    Anson, Blake
    Nuwaysir, Emile
    Swanson, Brad
    Wang, Wen Bo
    BIOPHARM INTERNATIONAL, 2011, 24 (03) : 58 - +
  • [32] Morpho-functional comparison of differentiation protocols to create iPSC-derived cardiomyocytes
    Nijak, Aleksandra
    Simons, Eline
    Vandendriessche, Bert
    Van de Sande, Dieter
    Fransen, Erik
    Sieliwonczyk, Ewa
    Van Gucht, Ilse
    Van Craenenbroeck, Emeline
    Saenen, Johan
    Heidbuchel, Hein
    Ponsaerts, Peter
    Labro, Alain J.
    Snyders, Dirk
    De Vos, Winnok
    Schepers, Dorien
    Alaerts, Maaike
    Loeys, Bart L.
    BIOLOGY OPEN, 2022, 11 (02):
  • [33] iPSC-Derived Cardiomyocytes as a Disease Model to Understand the Biology of Congenital Heart Defects
    Pushpan, Chithra K.
    Kumar, Subramanyan Ram
    CELLS, 2024, 13 (17)
  • [34] Advancements in techniques for human iPSC-derived cardiomyocytes maturation: mechanical and electrical stimulation approaches
    Lu, Yinsheng
    Liu, Yufeng
    Yan, Yumeng
    Fooladi, Saba
    Qyang, Yibing
    BIOPHYSICAL REVIEWS, 2025, 17 (01) : 169 - 183
  • [35] An impedance-based approach using human iPSC-derived cardiomyocytes significantly improves in vitro prediction of in vivo cardiotox liabilities
    Koci, Bryan
    Luerman, Gregory
    Duenbostell, Anika
    Kettenhofen, Ralf
    Bohlen, Heribert
    Coyle, Luke
    Knight, Brian
    Ku, Warren
    Volberg, Walter
    Woska, Joseph R., Jr.
    Brown, Martha P.
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 2017, 329 : 121 - 127
  • [36] Human iPSC-derived glia models for the study of neuroinflammation
    Stoberl, Nina
    Maguire, Emily
    Salis, Elisa
    Shaw, Bethany
    Hall-Roberts, Hazel
    JOURNAL OF NEUROINFLAMMATION, 2023, 20 (01)
  • [37] Generation of human iPSC-derived 3D bile duct within liver organoid by incorporating human iPSC-derived blood vessel
    Carolina, Erica
    Kuse, Yoshiki
    Okumura, Ayumu
    Aoshima, Kenji
    Tadokoro, Tomomi
    Matsumoto, Shinya
    Kanai, Eriko
    Okumura, Takashi
    Kasai, Toshiharu
    Yamabe, Souichiro
    Nishikawa, Yuji
    Yamaguchi, Kiyoshi
    Furukawa, Yoichi
    Tanimizu, Naoki
    Taniguchi, Hideki
    NATURE COMMUNICATIONS, 2024, 15 (01)
  • [38] Analyzing the α-Actinin Network in Human iPSC-Derived Cardiomyocytes Using Single Molecule Localization Microscopy
    Johann, Lisa
    Chabanovska, Oleksandra
    Lang, Cajetan Immanuel
    David, Robert
    Lemcke, Heiko
    JOVE-JOURNAL OF VISUALIZED EXPERIMENTS, 2020, (165):
  • [39] Engineered tissue geometry and Plakophilin-2 regulate electrophysiology of human iPSC-derived cardiomyocytes
    Simmons, Daniel W.
    Malayath, Ganesh
    Schuftan, David R.
    Guo, Jingxuan
    Oguntuyo, Kasoorelope
    Ramahdita, Ghiska
    Sun, Yuwen
    Jordan, Samuel D.
    Munsell, Mary K.
    Kandalaft, Brennan
    Pear, Missy
    Rentschler, Stacey L.
    Huebsch, Nathaniel
    APL BIOENGINEERING, 2024, 8 (01)
  • [40] Metabolic Maturation Increases Susceptibility to Hypoxia-induced Damage in Human iPSC-derived Cardiomyocytes
    Peters, Marijn C.
    Maas, Renee G. C.
    van Adrichem, Iris
    Doevendans, Pieter A. M.
    Mercola, Mark
    Saric, Tomo
    Buikema, Jan W.
    van Mil, Alain
    Chamuleau, Steven A. J.
    Sluijter, Joost P. G.
    Hnatiuk, Anna P.
    Neef, Klaus
    STEM CELLS TRANSLATIONAL MEDICINE, 2022, 11 (10) : 1040 - 1051