Icariin induces osteogenic differentiation in vitro in a BMP- and Runx2-dependent manner.

Published on May 2, 2008in Biochemical and Biophysical Research Communications2.985
· DOI :10.1016/J.BBRC.2008.02.054
Jiyuan Zhao3
Estimated H-index: 3
(UTokyo: University of Tokyo),
Shinsuke Ohba32
Estimated H-index: 32
(UTokyo: University of Tokyo)
+ 2 AuthorsTeruyuki Nagamune39
Estimated H-index: 39
(UTokyo: University of Tokyo)
Sources
Abstract
To effectively treat bone diseases using bone regenerative medicine, there is an urgent need to develop safe cheap drugs that can potently induce bone formation. Here, we demonstrate the osteogenic effect of icariin, the main active compound of Epimedium pubescens. Icariin induced osteogenic differentiation in pre-osteoblastic MC3T3-E1 cells and mouse primary osteoblasts. Icariin upregulated the mRNA expression levels of the osteoblast marker genes runt-related transcription factor 2 (Runx2) and inhibitor of DNA-binding 1 (Id-1). The osteogenic effect was inhibited by the introduction of Smad6 or dominant-negative Runx2, as well as Noggin treatment. Furthermore, icariin induced the mRNA expression of bone morphogenetic protein (BMP)-4. These data suggest that icariin exerts its potent osteogenic effect through induction of Runx2 expression, production of BMP-4 and activation of BMP signaling. The extremely low cost of icariin and its high abundance make it appealing for bone regenerative medicine.
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