<i>Panax Notoginseng</i> Saponins Promote Osteogenic Differentiation of Bone Marrow Stromal Cells Through the ERK and P38 MAPK Signaling Pathways
Author(s) -
Xuedong Li,
Zhao-yong Liu,
Bo-Jui Chang,
Dongxin Liu,
Bin Chen,
Chun Guo,
Yunguo Wang,
Jiankun Xu,
Dongyang Huang,
Shixin Du
Publication year - 2011
Publication title -
cellular physiology and biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.486
H-Index - 87
eISSN - 1421-9778
pISSN - 1015-8987
DOI - 10.1159/000331753
Subject(s) - panax notoginseng , mapk/erk pathway , bone sialoprotein , stromal cell , chemistry , alkaline phosphatase , microbiology and biotechnology , p38 mitogen activated protein kinases , signal transduction , bone marrow , osteoblast , osteocalcin , medicine , cancer research , biology , biochemistry , pathology , enzyme , alternative medicine , in vitro
The Chinese medicinal herb, Panax notoginseng, has long been used to treat bone fractures and Panax notoginseng saponins (PNS) could promote bone formation. Here, we investigated whether PNS could promote osteogenesis of bone marrow stromal cells (BMSCs) through modulating the MAPK signaling pathways, which are implicated in BMSC osteogenesis. We found that PNS markedly increased the mineralization of BMSCs by alizarin red S assays and stimulate alkaline phosphatase activity of these cells. Additionally, PNS significantly increased the mRNA levels of alkaline phosphatase, core-binding factor a1, and bone sialoprotein while decreasing PPARγ2 mRNA levels. Furthermore, inhibitors of ERK, PD98059, and p38, SB203580 inhibited the osteogenesis-potentiating effects by PNS. PNS stimulated the activation of ERK and p38 as evidenced by increased phosphorylation of these proteins, which was inhibited by PD98059 and SB203580. Our findings indicate that PNS could promote BMSC osteogenesis by activating the ERK and p38 signaling pathways.
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