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PMID: 29533735 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Space microgravity drives transdifferentiation of human bone marrow-derived mesenchymal stem cells from osteogenesis to adipogenesis.

Zhang C, Li L, Jiang Y, Wang C, Geng B, Wang Y, Chen J, Liu F, Qiu P, Zhai G, Chen P, Quan R, Wang J

Abstract

Bone formation is linked with osteogenic differentiation of mesenchymal stem cells (MSCs) in the bone marrow. Microgravity in spaceflight is known to reduce bone formation. In this study, we used a real microgravity environment of the SJ-10 Recoverable Scientific Satellite to examine the effects of space microgravity on the osteogenic differentiation of human bone marrow-derived mesenchymal stem cells (hMSCs). hMSCs were induced toward osteogenic differentiation for 2 and 7 d in a cell culture device mounted on the SJ-10 satellite. The satellite returned to Earth after going through space experiments in orbit for 12 d, and cell samples were harvested and analyzed for differentiation potentials. The results showed that space microgravity inhibited osteogenic differentiation and resulted in adipogenic differentiation, even under osteogenic induction conditions. Under space microgravity, the expression of 10 genes specific for osteogenesis decreased, including collagen family members, alkaline phosphatase ( ALP), and runt-related transcription factor 2 ( RUNX2), whereas the expression of 4 genes specific for adipogenesis increased, including adipsin ( CFD), leptin ( LEP), CCAAT/enhancer binding protein β ( CEBPB), and peroxisome proliferator-activated receptor-γ ( PPARG). In the analysis of signaling pathways specific for osteogenesis, we found that the expression and activity of RUNX2 was inhibited, expression of bone morphogenetic protein-2 ( BMP2) and activity of SMAD1/5/9 were decreased, and activity of focal adhesion kinase (FAK) and ERK-1/2 declined significantly under space microgravity. These data indicate that space microgravity plays a dual role by decreasing RUNX2 expression and activity through the BMP2/SMAD and integrin/FAK/ERK pathways. In addition, we found that space microgravity increased p38 MAPK and protein kinase B (AKT) activities, which are important for the promotion of adipogenic differentiation of hMSCs. Space microgravity significantly decreased the expression of Tribbles homolog 3 ( TRIB3), a repressor of adipogenic differentiation. Y15, a specific inhibitor of FAK activity, was used to inhibit the activity of FAK under normal gravity; Y15 decreased protein expression of TRIB3. Therefore, it appears that space microgravity decreased FAK activity and thereby reduced TRIB3 expression and derepressed AKT activity. Under space microgravity, the increase in p38 MAPK activity and the derepression of AKT activity seem to synchronously lead to the activation of the signaling pathway specifically promoting adipogenesis.-Zhang, C., Li, L., Jiang, Y., Wang, C., Geng, B., Wang, Y., Chen, J., Liu, F., Qiu, P., Zhai, G., Chen, P., Quan, R., Wang, J. Space microgravity drives transdifferentiation of human bone marrow-derived mesenchymal stem cells from osteogenesis to adipogenesis.

Keywords
RNA-SEQ SJ-10 satellite hMSCs signaling pathway
MeSH 主题词
Adipogenesis/physiology Alkaline Phosphatase/metabolism Bone Marrow/metabolism,physiology Cell Differentiation/physiology Cell Transdifferentiation/physiology Cells, Cultured Core Binding Factor Alpha 1 Subunit/metabolism Humans Mesenchymal Stem Cells/physiology Osteogenesis/physiology Proto-Oncogene Proteins c-akt/metabolism Signal Transduction/physiology Space Flight/methods Weightlessness p38 Mitogen-Activated Protein Kinases/metabolism
化学物质
Core Binding Factor Alpha 1 Subunit Proto-Oncogene Proteins c-akt p38 Mitogen-Activated Protein Kinases Alkaline Phosphatase
作者与单位
共 13 位作者,点击展开单位 / ORCID
Zhang Cui
Institute of Cell and Development Biology, College of Life Sciences, Zijingang Campus, Zhejiang University, Hangzhou, China.
Li Liang
Institute of Cell and Development Biology, College of Life Sciences, Zijingang Campus, Zhejiang University, Hangzhou, China.
Jiang Yuanda
National Center of Space Science, Chinese Academy of Sciences, Beijing, China.
Wang Cuicui
Institute of Cell and Development Biology, College of Life Sciences, Zijingang Campus, Zhejiang University, Hangzhou, China.
Geng Baoming
National Center of Space Science, Chinese Academy of Sciences, Beijing, China.
Wang Yanqiu
National Center of Space Science, Chinese Academy of Sciences, Beijing, China.
Chen Jianling
Institute of Cell and Development Biology, College of Life Sciences, Zijingang Campus, Zhejiang University, Hangzhou, China.
Liu Fei
Institute of Orthopedics, Xiaoshan Traditional Chinese Medical Hospital, Hangzhou, China.
Qiu Peng
National Center of Space Science, Chinese Academy of Sciences, Beijing, China.
Zhai Guangjie
National Center of Space Science, Chinese Academy of Sciences, Beijing, China.
Chen Ping
Department of Cell Biology, Emory University School of Medicine, Atlanta, Georgia, USA. | Department of Otolaryngology, Emory University School of Medicine, Atlanta, Georgia, USA.
Quan Renfu
Institute of Orthopedics, Xiaoshan Traditional Chinese Medical Hospital, Hangzhou, China.
Wang Jinfu
Institute of Cell and Development Biology, College of Life Sciences, Zijingang Campus, Zhejiang University, Hangzhou, China.
Article Info
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Abbr.
FASEB J
ISSN
1530-6860
Published
2018-00-00
电子出版
2018-00-13
页码
4444-4458
Language
English
Country/Region
United States
NLM ID
8804484
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