The effect of simvastatin on the proliferation and differentiation of human bone marrow stromal cells

被引:89
作者
Baek, KH
Lee, WY
Oh, KW
Tae, HJ
Lee, JM
Lee, EJ
Han, JH
Kang, MI
Cha, BY
Lee, KW
Son, HY
Kang, SK
机构
[1] Catholic Univ Korea, Coll Med, Dept Internal Med, Seoul, South Korea
[2] Sungkyunkwan Univ, Kangbuk Samsung Hosp, Sch Med, Seoul, South Korea
[3] Hallym Univ, Pyungchon Sacred Heart Hosp, Coll Med, Anyang, South Korea
关键词
simvastatin; osteoblasts; cell proliferation; cell differentiation; bone marrow cells; stromal cells;
D O I
10.3346/jkms.2005.20.3.438
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Statins have been postulated to affect the bone metabolism. Recent experimental and epidemiologic studies have suggested that statins may also have bone protective effects. This study assessed the effects of simvastatin on the proliferation and differentiation of human bone marrow stromal cells (BMSCs) in an ex vivo culture. The bone marrow was obtained from healthy donors. Mononuclear cells were isolated and cultured to osteoblastic lineage. In the primary culture, 10(-6) simvastatin diminished the mean size of the colony forming units-fibroblastic (CFU-Fs) and enhanced matrix calcification. At near confluence, the cells were sub-cultured. Thereafter, the alkaline phosphatase (ALP) activities of each group were measured by the time course of the secondary culture. Simvastatin increased the ALP activity in a dose dependent manner, and this stimulatory effect was more evident during the early period of culture. A 3-[4, 5-dimethylthiazol-2-yl]-2, 5-diphenyltetrazolium bromide (MTT) assay was performed during the secondary culture in order to estimate the effect of simvastatin on the proliferation of human. When compared to the control group, simvastatin significantly decreased the proliferation of cells of each culture well. 10(-6) of simvastatin also significantly enhanced the osteocalcin expression level. This study shows that simvastatin has a stimulatory effect on bone formation through osteoblastic differentiation, and has an inhibitory effect on the proliferative potential of human BMSCs.
引用
收藏
页码:438 / 444
页数:7
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