Drynaria fortunei J. Sm. promotes osteoblast maturation by inducing differentiation-related gene expression and protecting against oxidative stress-induced apoptotic insults

被引:39
作者
Hung, Tai-Yuan [2 ,3 ]
Chen, Ta-Liang [4 ]
Liao, Mei-Hsiu
Ho, Wei-Pin [3 ]
Liu, Der-Zen [5 ]
Chuang, Wu-Chang [6 ]
Chen, Ruei-Ming [1 ,3 ]
机构
[1] Taipei Med Univ, Grad Inst Med Sci, Coll Med, Taipei 110, Taiwan
[2] Yuans Gen Hosp, Dept Orthoped Surg, Kaohsiung, Taiwan
[3] Taipei Med Univ Wan Fang Hosp, Cell Physiol & Mol Image Res Ctr, Taipei, Taiwan
[4] Taipei Med Univ Hosp, Dept Anesthesiol, Taipei, Taiwan
[5] Taipei Med Univ, Grad Inst Biomed Mat & Engn, Taipei 110, Taiwan
[6] Brion Res Inst Taiwan, Taipei, Taiwan
关键词
Drynaria fortunei J. Sm; Osteoblast maturation; Gene expression; Anti-apoptosis; BONE; GROWTH; PROLIFERATION; ACTIVATION; EXTRACT;
D O I
10.1016/j.jep.2010.05.063
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Aim of the study: Drynaria fortunei J. Sm. is one variety of the traditional Chinese medical herb Gusuibu. This study was aimed to evaluate the effects of water extracts of Kunze on regulation of osteoblast maturation and its possible mechanisms. Materials and methods: Primary osteoblasts prepared from neonatal rat calvarias were exposed to the water extracts of Kunze (WEK), and the cytotoxicity was assayed. Osteoblast maturation was evaluated by analyzing cell mineralization. RT-PCR was executed to determine the effects of WEK on regulation of osteoblast differentiation-related gene expression. Nitrosative stress and apoptotic cells were quantified using flow cytometry. Results: Exposure of rat calvarial osteoblasts to WEK did not affect cell viability, but significantly promoted osteoblast mineralization. WEK induced osteoprogenitor proliferation-related insulin-like growth factor-1 mRNA, but did not affect collagen type 1 mRNA expression. Treatment with WEK likewise induced the expression of matrix maturation-related bone morphogenetic protein (BMP)-2 and BMP-6 mRNA. Consequently, WEK enhanced the levels of mineralization-related alkaline phosphatase, ostepontin, and osteocalcin mRNA in osteoblasts. In addition, exposure of osteoblasts to WEK alleviated nitrosative stress-caused apoptotic insults. Conclusions: This study shows that WEK can promote osteoblast maturation by regulating bone differentiation-related gene expression and defending against nitrosative stress-induced apoptotic insults. (C) 2010 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:70 / 77
页数:8
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