Skip to main content
Log in

Achyranthes bidentata Saponins Promote Osteogenic Differentiation of Bone Marrow Stromal Cells Through the ERK MAPK Signaling Pathway

  • Original Paper
  • Published:
Cell Biochemistry and Biophysics Aims and scope Submit manuscript

Abstract

Achyranthes bidentata, is a herbal plant commonly used in the treatment of osteoporosis and bone nonunion in the Traditional Chinese Medicine. Saponins are the major compounds extracted from Achyranthes bidentata that have been shown to exert various pharmacological activities such as anti-inflammatory, antipyretic, antirheumatic, diuretic, and anti-osteoporosis. The Achyranthes bidentata saponins (ABS) were found to induce proliferation and differentiation in bone marrow stromal cells (BMSCs) as determined by the cell proliferation and alkaline phosphatase assays. Also, following the osteogenic induction, cells treated with ABS showed increased mRNA levels of rat bone morphogenetic protein-2, runt-related transcription factor 2, and osterix. Furthermore, ABS stimulated the activation of ERK as evidenced by increased phosphorylation of these proteins, which was blocked by an inhibitor of ERK (PD98059). Taken together, these results suggest that ABS stimulated osteogenic differentiation of BMSCs via activation of the ERK signaling pathway.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  1. Niu, Y., Li, Y., Huang, H., Kong, X., Zhang, R., Liu, L., et al. (2011). Asperosaponin VI, a saponin component from Dipsacus asper wall, induces osteoblast differentiation through bone morphogenetic protein-2/p38 and extracellular signal-regulated kinase 1/2 pathway. Phytotherapy Research, 25(11), 1700–1706.

    Article  CAS  PubMed  Google Scholar 

  2. Licata, A. A. (2005). Discovery, clinical development, and therapeutic uses of bisphosphonates. Annals of Pharmacotherapy, 39, 668–677.

    Article  CAS  PubMed  Google Scholar 

  3. Zhang, P., Dai, K. R., Yan, S. G., Yan, W. Q., Zhang, C., Chen, D. Q., et al. (2009). Effects of naringin on the proliferation and osteogenic differentiation of human bone mesenchymal stem cell. European Journal of Pharmacology, 607(1–3), 1–5.

    Article  CAS  PubMed  Google Scholar 

  4. Berger, I., Piecha, G., Rabkin, R., Kaya, N., Geldyyev, A., Sun, D., et al. (2007). Growth hormone treatment prevents osteoporosis in uremic rats. Histology Histopathology, 22(11), 1231–1239.

    CAS  PubMed  Google Scholar 

  5. Luhe, A., Kunkele, K. P., Haiker, M., Schad, K., Zihlmann, C., Bauss, F., et al. (2008). Preclinical evidence for nitrogen-containing bisphosphonate inhibition of farnesyl diphosphate (FPP) synthase in the kidney: Implications for renal safety. Toxicology in Vitro, 22(4), 899–909.

    Article  CAS  PubMed  Google Scholar 

  6. Nikolov, S., Thuan, N., & Zheljazkov, V. (1996). Flavonoids from Achyranthes Bidentata BC. Acta Horticulturae, 426, 75–78.

    Google Scholar 

  7. Shi, C. J., Zhou, Y. D., Zhang, J. B., & Tian, G. Y. (2006). Researches of polysaccharides from Achyrnthes bidentata. Chinese Journal of New Drug, 15, 1330–1334.

    CAS  Google Scholar 

  8. Li, J. X., Hareyama, T., Tezuka, Y., Zhang, Y., Miyahara, T., & Kadota, S. (2005). Five new oleanolic acid glycosides from Achyranthes bidentata with inhibitory activity on osteoclast formation. Planta Medica, 71(7), 673–679.

    Article  CAS  PubMed  Google Scholar 

  9. Wattel, A., Kamel, S., Prouillet, C., Petit, J. P., Lorget, F., Offord, E., et al. (2004). Flavonoid quercetin decreases osteoclastic differentiation induced by RANKL via a mechanism involving NF kappa B and AP-1. Journal of Cellular Biochemistry, 92(2), 285–295.

    Article  CAS  PubMed  Google Scholar 

  10. Meng, D. L., & Li, X. (2001). The research development in the chemical constituents and pharmacological activities of Achyranthes bidentata Bl. Chinese Journal of Medicinal Chemistry, 11, 120–124.

    CAS  Google Scholar 

  11. Yuan, Y. J., Cui, Y., Yu, Y., & Yong, Y. H. (2002). Different mechanisms mediate the exciting effect about Achyranthes bidentataon the spike activity of the uterine smooth muscle in virgin rats. Journal of Veterinary Science and Technology, 32(12), 8–12.

    Google Scholar 

  12. Zhang, W. X., Yang, S. L., Zhang, X. S., Xue, D. M., Zhang, S. L., & Wei, J. D. (2002). The relationship between anti-implantation of Achyranthes bidentata Bl. and mast cell in the uterus. Chinese Journal of Immunology, 18(7), 492–495.

    CAS  Google Scholar 

  13. Wang, Y. F., Wang, Q. D., Liu, C. J., Jiang, J. H., Sun, W. X., & Xia, W. (1997). Antitumor activity of the crude saponins from Achyranthes bidentata.  Journal of Henan Medical University, 32(4), 4–6.

    CAS  Google Scholar 

  14. Gao, C. K., Gao, J., Ma, R. L., Xu, X. X., Huang, P., & Ni, S. D. (2003). Research on analgesic and anti-inflammatory and invigorate circulation effects of total saponins of Achyranthes. Anhui Medical of Pharmaceutical Journal, 7(4), 248–249.

    Google Scholar 

  15. Liu, X. P., Chen, F. L., & Cheng, Y. J. (2005). Study of total isoflavone from Astragalus membranaceous on the prevention of osteoporosis in rats. Zhejiang JITCWM, 15(5), 282–283.

    Google Scholar 

  16. Ren, X. C., Xu, X. X., Xu, D. J., & Gao, J. (2011). Effects of Achyranthes bidentata saponins on bone metabolism of osteoporosis rats induced by retinoic acid. Chinese Journal of Experimental Traditional Medical Formulae, 17(4), 128–130.

    Google Scholar 

  17. Pearson, G., Robinson, F., Beers Gibson, T., Xu, B. E., Karandikar, M., Berman, K., et al. (2001). Mitogen-activated protein (MAP) kinase pathways: Regulation and physiological functions. Endocrine Reviews, 22(2), 153–183.

    CAS  PubMed  Google Scholar 

  18. Jaiswal, R. K., Jaiswal, N., Bruder, S. P., Mbalaviele, G., Marshak, D. R., & Pittenger, M. F. (2000). Adult human mesenchymal stem cell differentiation to the osteogenic or adipogenic lineage is regulated by mitogen-activated protein kinase. Journal of Biological Chemistry, 275(13), 9645–9652.

    Article  CAS  PubMed  Google Scholar 

  19. Sale, E. M., Atkinson, P. G., & Sale, G. J. (1995). Requirement of MAP kinase for differentiation of fibroblasts to adipocytes, for insulin activation of p90 S6 kinase and for insulin or serum stimulation of DNA synthesis. EMBO Journal, 14(4), 674–684.

    CAS  PubMed Central  PubMed  Google Scholar 

  20. Komori, T., Yagi, H., Nomura, S., Yamaguchi, A., Sasaki, K., Deguchi, K., et al. (1977). Targeted disruption of Cbfa1 results in a complete lack of bone formation owing to maturational arrest of osteoblast. Cell, 89(5), 755–764.

    Article  Google Scholar 

  21. Nakashima, K., Zhou, X., Kunkel, G., Zhang, Z., Deng, J., Behringer, R., et al. (2002). The novel zinc finger-containing transcription factor osterix is required for osteoblast differentiation and bone formation. Cell, 108(1), 17–29.

    Article  CAS  PubMed  Google Scholar 

  22. Nishio, Y., Dong, Y., Paris, M., OKeefe, R. J., Schwarz, E. M., & Drissi, H. (2006). Runx2-mediated regulation of the zinc finger Osterix/Sp7 gene. Gene, 372, 62–70.

    Article  CAS  PubMed  Google Scholar 

  23. Lee, M. H., Kim, Y. J., Kim, H. J., Park, H. D., Kang, A. R., Kyung, H. M., et al. (2003). BMP-2-induced Runx2 expression is mediated by Dlx5, and TGF-beta 1 opposes the BMP-2-induced osteoblast differentiation by suppression of Dlx5 expression. Journal of Biological Chemistry, 278(36), 34387–34394.

    Article  CAS  PubMed  Google Scholar 

  24. Turjanski, A. G., Vaque, J. P., & Gutkind, J. S. (2007). MAP kinases and the control of nuclear events. Oncogene, 26(22), 3240–3253.

    Article  CAS  PubMed  Google Scholar 

  25. Kirkham, G. R., & Cartmell, S. H. (2007). Genes and proteins involved in the regulation of osteogenesis. In: N. Ashammakhi, R. Reis & Chiellini E (Eds.). Topics in Tissue Engineering, vol. 3.

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hu Zhang.

Rights and permissions

Reprints and permissions

About this article

Cite this article

He, G., Guo, W., Lou, Z. et al. Achyranthes bidentata Saponins Promote Osteogenic Differentiation of Bone Marrow Stromal Cells Through the ERK MAPK Signaling Pathway. Cell Biochem Biophys 70, 467–473 (2014). https://doi.org/10.1007/s12013-014-9942-3

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s12013-014-9942-3

Keywords

Navigation