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Ethanol extract of Lithospermum erythrorhizon Sieb. et Zucc. promotes osteoblastogenesis through the regulation of Runx2 and Osterix

Authors :
Soo Im Choi
You Hee Choi
Sun Woo Jin
Geum Soog Kim
Dae Young Lee
Young Sup Ahn
Kwang Youl Lee
Jae Ho Choi
Hyung Gyun Kim
Hye Gwang Jeong
Seung Yu Kim
Younho Han
Source :
International Journal of Molecular Medicine. 38:610-618
Publication Year :
2016
Publisher :
Spandidos Publications, 2016.

Abstract

Bone remodeling and homeostasis are largely the result of the coordinated action of osteoblasts and osteoclasts. Osteoblasts are responsible for bone formation. The differentiation of osteoblasts is regulated by the transcription factors, Runx2 and Osterix. Natural products of plant origin are still a major part of traditional medicinal systems in Korea. The root of Lithospermum erythrorhizon Sieb. et Zucc. (LR), the purple gromwell, is an herbal medicine used for inflammatory and infectious diseases. LR is an anti-inflammatory and exerts anticancer effects by inducing the apoptosis of cancer cells. However, the precise molecular signaling mechanisms of osteoblastogenesis as regards LR and osteoblast transcription are not yet known. In this study, we investigated the effects of ethanol (EtOH) extract of LR (LES) on the osteoblast differentiation of C2C12 myoblasts induced by bone morphogenetic protein 4 (BMP4) and the potential involvement of Runx2 and Osterix in these effects. We found that the LES exhibited an ability to induce osteoblast differentiation. LES increased the expression of the osteoblast marker, alkaline phosphatase (ALP), as well as its activity, as shown by ALP staining and ALP activity assay. LES also increased mineralization, as shown by Alizarin Red S staining. Treatment with LES increased the protein levels (as shown by immunoblotting), as well as the transcriptional activity of Runx2 and Osterix and enhanced osteogenic activity. These results suggest that LES modulates osteoblast differentiation at least in part through Runx2 and Osterix.

Details

ISSN :
1791244X and 11073756
Volume :
38
Database :
OpenAIRE
Journal :
International Journal of Molecular Medicine
Accession number :
edsair.doi.dedup.....bc809c4091f43021a7e8b47f5176cfa2
Full Text :
https://doi.org/10.3892/ijmm.2016.2655