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密鳞赤鳞蕨通过诱导分化相关基因表达和抵御氧化应激诱导的凋亡损伤促进成骨细胞成熟。

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

机构信息

Department of Orthopedic Surgery, Yuan's General Hospital, Kaohsiung, Taiwan.

出版信息

J Ethnopharmacol. 2010 Aug 19;131(1):70-7. doi: 10.1016/j.jep.2010.05.063. Epub 2010 Jun 8.

Abstract

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.

摘要

研究目的

密鳞鳞毛蕨(Drynaria fortunei J. Sm.)是中国传统草药骨碎补的一个品种。本研究旨在评估昆氏水提取物对成骨细胞成熟的调节作用及其可能的机制。

材料与方法

从新生大鼠颅骨中制备原代成骨细胞,并用昆氏水提取物(WEK)处理,检测细胞毒性。通过分析细胞矿化来评估成骨细胞的成熟程度。通过 RT-PCR 确定 WEK 对成骨细胞分化相关基因表达的调节作用。使用流式细胞术定量测定硝化应激和凋亡细胞。

结果

WEK 暴露于大鼠颅骨成骨细胞不会影响细胞活力,但显著促进成骨细胞矿化。WEK 诱导成骨前体细胞增殖相关胰岛素样生长因子-1mRNA,但不影响胶原 I 型 mRNA 的表达。WEK 处理同样诱导基质成熟相关骨形态发生蛋白(BMP)-2 和 BMP-6 mRNA 的表达。因此,WEK 增强了成骨细胞中矿化相关碱性磷酸酶、骨桥蛋白和骨钙素 mRNA 的水平。此外,WEK 减轻了成骨细胞中硝化应激引起的凋亡损伤。

结论

本研究表明,WEK 可以通过调节骨分化相关基因表达和抵御硝化应激诱导的凋亡损伤来促进成骨细胞成熟。

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