Fermented ginseng extract, BST204, disturbs adipogenesis of mesenchymal stem cells through inhibition of S6 kinase 1 signaling.

作者: Sang Ah Yi , Jieun Lee , Sun Kyu Park , Jeom Yong Kim , Jong Woo Park

DOI: 10.1016/J.JGR.2018.08.002

关键词:

摘要: Abstract Background The biological and pharmacological effects of BST204, a fermented ginseng extract, have been reported in various disease conditions. However, its molecular action metabolic remains poorly understood. In this study, we identified the antiadipogenic activity BST204 resulting from inhibition S6 kinase 1 (S6K1) signaling pathway. Methods inhibitory on S6K1 were investigated by immunoblot, nuclear fractionation, immunoprecipitation analyses. effect was evaluated measuring mRNA levels adipogenic genes chromatin quantitative real-time polymerase chain reaction analysis. Results Treatment with inhibited activation translocation S6K1, further decreasing interaction between histone H2B 10T1/2 mesenchymal stem cells. Subsequently, phosphorylation at serine 36 (H2BS36p) reduced inducing an increase expression Wnt6, Wnt10a, Wnt10b, which disturbed differentiation promoted myogenic early osteogenic gene expression. Consistently, treatment during commitment suppressed marker lipid drop formation. Conclusion Our results indicate that blocks adipogenesis cells through S6K1-mediated phosphorylation. This study suggests potential therapeutic strategy using to combat obesity musculoskeletal diseases.

参考文章(51)
Li-hua Yin, Wen-xiao Cheng, Zi-shun Qin, Ke-mo Sun, Mei Zhong, Jia-kui Wang, Wei-yue Gao, Zhan-hai Yu, Effects of ginsenoside Rg-1 on the proliferation and osteogenic differentiation of human periodontal ligament stem cells Chinese Journal of Integrative Medicine. ,vol. 21, pp. 676- 681 ,(2015) , 10.1007/S11655-014-1856-9
Kai Ge, Epigenetic regulation of adipogenesis by histone methylation Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. ,vol. 1819, pp. 727- 732 ,(2012) , 10.1016/J.BBAGRM.2011.12.008
Hai Dan Yuan, Hai Yan Quan, Mi-Song Jung, Su-Jung Kim, Bo Huang, Do-Yeon Kim, Sung-Hyun Chung, Anti-Diabetic Effect of Pectinase-Processed Ginseng Radix (GINST) in High Fat Diet-Fed ICR Mice Journal of Ginseng Research. ,vol. 35, pp. 308- 314 ,(2011) , 10.5142/JGR.2011.35.3.308
I. Ben-Sahra, J. J. Howell, J. M. Asara, B. D. Manning, Stimulation of de Novo Pyrimidine Synthesis by Growth Signaling Through mTOR and S6K1 Science. ,vol. 339, pp. 1323- 1328 ,(2013) , 10.1126/SCIENCE.1228792
Jin-Taek Hwang, Myoung-Su Lee, Hyun-Jin Kim, Mi-Jeong Sung, Hye Young Kim, Myung Sunny Kim, Dae Young Kwon, Antiobesity effect of ginsenoside Rg3 involves the AMPK and PPAR‐γ signal pathways Phytotherapy Research. ,vol. 23, pp. 262- 266 ,(2009) , 10.1002/PTR.2606
J. L. Owen, Y. Zhang, S.-H. Bae, M. S. Farooqi, G. Liang, R. E. Hammer, J. L. Goldstein, M. S. Brown, Insulin stimulation of SREBP-1c processing in transgenic rat hepatocytes requires p70 S6-kinase Proceedings of the National Academy of Sciences of the United States of America. ,vol. 109, pp. 16184- 16189 ,(2012) , 10.1073/PNAS.1213343109
Heejung Yang, Guijae Yoo, Hye Seong Kim, Jeom Yong Kim, Sun Ok Kim, Young Hyo Yoo, Sang Hyun Sung, Implication of the stereoisomers of ginsenoside derivatives in the antiproliferative effect of HSC-T6 cells. Journal of Agricultural and Food Chemistry. ,vol. 60, pp. 11759- 11764 ,(2012) , 10.1021/JF303714C
Xiaoju Max Ma, John Blenis, Molecular mechanisms of mTOR-mediated translational control Nature Reviews Molecular Cell Biology. ,vol. 10, pp. 307- 318 ,(2009) , 10.1038/NRM2672
H. Huang, T.-J. Song, X. Li, L. Hu, Q. He, M. Liu, M. D. Lane, Q.-Q. Tang, BMP signaling pathway is required for commitment of C3H10T1/2 pluripotent stem cells to the adipocyte lineage Proceedings of the National Academy of Sciences of the United States of America. ,vol. 106, pp. 12670- 12675 ,(2009) , 10.1073/PNAS.0906266106
Dong-Hyun Kwon, Shambhunath Bose, Mi-Young Song, Myeong-Jong Lee, Chi-Yeon Lim, Bum-Sun Kwon, Ho-Jun Kim, Efficacy of Korean Red Ginseng by Single Nucleotide Polymorphism in Obese Women: Randomized, Double-blind, Placebo-controlled Trial Journal of Ginseng Research. ,vol. 36, pp. 176- 189 ,(2012) , 10.5142/JGR.2012.36.2.176