Icariin promotes bone formation via the BMP-2/Smad4 signal transduction pathway in the hFOB 1.19 human osteoblastic cell line.

@article{Liang2012IcariinPB,
  title={Icariin promotes bone formation via the BMP-2/Smad4 signal transduction pathway in the hFOB 1.19 human osteoblastic cell line.},
  author={Wenna Liang and Mu-nan Lin and Xi-hai Li and Candong Li and Bizhen Gao and Huijuan Gan and Zhaoyang Yang and Xuejuan Lin and Linghong Liao and Min Yang},
  journal={International journal of molecular medicine},
  year={2012},
  volume={30 4},
  pages={
          889-95
        }
}
Icariin, the main active compound of the traditional Chinese medicine, Epimedium, is commonly used for the clinical treatment of osteoporosis. However, the precise molecular mechanism of the therapeutic effect of icariin has not been elucidated. The aim of this study was to examine the effect of icariin on cell viability, alkaline phosphatase (ALP) activity, the amount of calcified nodules, and to delineate the molecular mechanism of icariin-enhanced bone formation by investigating the… 

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References

SHOWING 1-10 OF 58 REFERENCES

Icariin stimulates MC3T3-E1 cell proliferation and differentiation through up-regulation of bone morphogenetic protein-2.

Investigation of the osteogenic effects of icariin in an undifferentiated osteoblast cell line by detecting cell morphology, viability, cell cycling and bone morphogenetic protein-2 (BMP-2) expression found it to promote osteoblasts proliferation and differentiation in vitro.

Icariin enhances the osteogenic differentiation of bone marrow stromal cells but has no effects on the differentiation of newborn calvarial osteoblasts of rats.

It is indicated that icariin may exert bone-strengthening activity by enhancing the osteogenic differentiation of MSCs, which partially explains the anti-osteoporosis action of Epimedium herb.

Icariin is more potent than genistein in promoting osteoblast differentiation and mineralization in vitro

In vitro studies have demonstrated that icariin has a stronger osteogenic activity than genistein, while the prenyl group on C‐8 of icARIin could be the active group that takes part in osteoblastic differentiation and explains its greater potency in osteogenesis, mechanisms of action, and reasons for the relative potency of icariIn need to be further studied.

BMP2 Regulates Osterix through Msx2 and Runx2 during Osteoblast Differentiation*

Osterix is regulated via both Runx2-dependent and -independent mechanisms, and that Osterix controls osteoblast differentiation, at least in part, by regulating the expression of genes not controlled by Runx 2.

Involvement of BMPs/Smad Signaling Pathway in Mechanical Response in Osteoblasts

It is found that mechanical strain enhanced alkaline phosphatase (ALP) expression and activated BMPs/Smad signaling pathway and the protein levels of Smad1 and Smad5, but not their mRNA levels, were up-regulated by mechanical strain.
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