A traditional Chinese medicine formula extracts stimulate proliferation and inhibit mineralization of human mesenchymal stem cells in vitro

被引:21
作者
Chen, Muwan [1 ,2 ,3 ]
Feng, Wenzhou [1 ,2 ]
Cao, Hui [4 ,5 ]
Zou, Lijin [3 ]
Chen, Chungui [4 ,5 ]
Baatrup, Anette [3 ]
Nielsen, Anne Bay [3 ]
Li, Haisheng [3 ]
Kassem, Moustapha [6 ]
Zou, Xuenong [1 ,2 ,3 ]
Bunger, Cody [3 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 1, Dept Orthopaed, Guangzhou 510080, Guangdong, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 5, Dept Pharm, Guangzhou 510080, Guangdong, Peoples R China
[3] Aarhus Univ Hosp, Orthopaed Res Lab, DK-8000 Aarhus C, Denmark
[4] Sun Yat Sen Univ, Natl Engn Res Ctr Modernizat Tradit Chinese Med, Guangzhou 510275, Guangdong, Peoples R China
[5] Sun Yat Sen Univ, Sch Life Sci, Guangzhou 510275, Guangdong, Peoples R China
[6] Odense Univ Hosp, Dept Endocrinol & Metab, DK-5000 Odense C, Denmark
关键词
TCM extracts; Human mesenchymal stem cell; Cell proliferation; Osteogenic differentiation; Osteoarthritis; MARROW STROMAL CELLS; SUBCHONDRAL BONE; OSTEOBLASTIC DIFFERENTIATION; OSTEOGENIC DIFFERENTIATION; INVERSE RELATIONSHIP; GROWTH-FACTORS; OSTEOARTHRITIS; OSTEOPOROSIS; DEGRADATION; PROGRESSION;
D O I
10.1016/j.jep.2009.06.013
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Aim of the study: To investigate the effects of a traditional Chinese medicine (TCM) formula extract, named as ZD-I, on the proliferation and osteogenic differentiation of human mesenchymal stem cells (hMSCs) in vitro. Materials and methods: When hMSCs cultivated in the basal medium with ZD-I, cell viability was assessed by MTT assay and cellular proliferation was assessed by SYBR green I assay. The effects of ZD-I on osteogenic differentiation of hMSCs were assessed by alkaline phosphatase (ALP) activity, mineralization assay and real-time RT-PCR. Results: ZD-I (0.78-100 mu g/ml) was non-cytotoxic. The 50% inhibitory concentration (IC50) of hMSCs was 200 mu g/ml. ZD-I (0.78-50 mu g/ml) stimulated the proliferation of hMSCs. ZD-I did not change ALP activity of hMSCs cultivated in osteogenic medium in the early stage (4 and 7 days), but ZD-I inhibited the mineralization of hMSCs through down-regulation of several osteogenic markers (e.g. osteocalcin, bone morphogenetic protein 2 and osteopontin) in the late stage. Conclusions: ZD-I stimulate cellular proliferation and decrease the bone mineral deposition of hMSCs. These results suggest ZD-I may play an important therapeutic role in osteoarthritic patients by improving proliferative capacity of hMSCs and inhibiting the mineralization of hMSCs. (C) 2009 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:75 / 82
页数:8
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