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淫羊藿苷II促进大鼠骨髓间充质干细胞成骨分化过程中诱导型一氧化氮合酶和一氧化氮的变化

[The changes of iNOS and NO in the osteogenic differentiation process of rat bone marrow stromal cells promoted by icariside II].

作者信息

Zhai Yuan-kun, Chen Ke-ming, Ge Bao-feng, Ma Hui-ping, Ming Lei-guo, Cheng Guo-zheng

机构信息

Institute of Orthopaedics, Lanzhou General Hospital, Lanzhou Command, PLA, Lanzhou 730050, China.

出版信息

Yao Xue Xue Bao. 2011 Apr;46(4):383-9.

Abstract

This study is to investigate the effects on the expression of iNOS and production of NO in the osteogenic differentiation process of rat bone marrow stromal cells (rBMSCs) by icariside II. rBMSCs were cultured by adherence screening method. When the culture dishes were covered with 80% cells, the osteogenic induced cultures were adopted. Icariside II was supplemented into the culture at 1 x 10(-5) mol x L(-1). The activity of iNOS, content of NO and osteogenic differentiation markers including alkaline phosphatase (ALP) activity, CFU-FALP and mineralized bone nodules were compared among the icariside II-supplemented group, L-NMAE group, icariside II + L-NAME group and the control. Total RNA was isolated and the gene expression of iNOS, Osterix and Runx-2 was investigated by real-time PCR. Total protein was also isolated and the secretion of iNOS and collagen I was examined by Western blotting. Icariside II can significantly improved ALP activity, CFU-FALP amount and mineralized nodules. Besides, the mRNA level of factors related to the osteogenic differentiation includes Osterix and Runx-2 also enhanced. The secretion of collagen I also promoted significantly. But all of these effects can be inhibited by L-NAME which can specifically inhibit the activity of iNOS. Icariside II enhances the osteogenic differentiation of rBMSCs significantly, but if the activity of iNOS was blocked by L-NAME, the osteogenic differentiation markers decrease accompanied with iNOS and NO decrease, suggesting that icariside II stimulates the osteogenic differentiation via enhancing the activity of iNOS and promoting the generation of NO.

摘要

本研究旨在探讨淫羊藿次苷II对大鼠骨髓间充质干细胞(rBMSCs)成骨分化过程中诱导型一氧化氮合酶(iNOS)表达及一氧化氮(NO)生成的影响。采用贴壁筛选法培养rBMSCs。当培养皿中细胞铺满80%时,进行成骨诱导培养。将淫羊藿次苷II以1×10⁻⁵ mol·L⁻¹的浓度加入培养基中。比较淫羊藿次苷II添加组、L - NMAE组、淫羊藿次苷II + L - NAME组和对照组中iNOS的活性、NO的含量以及成骨分化标志物,包括碱性磷酸酶(ALP)活性、CFU - FALP和矿化骨结节。提取总RNA,通过实时PCR检测iNOS、Osterix和Runx - 2的基因表达。同时提取总蛋白,通过蛋白质免疫印迹法检测iNOS和I型胶原蛋白的分泌情况。淫羊藿次苷II可显著提高ALP活性、CFU - FALP数量和矿化结节。此外,与成骨分化相关的因子如Osterix和Runx - 2的mRNA水平也有所提高。I型胶原蛋白的分泌也显著增加。但L - NAME可特异性抑制iNOS的活性,从而抑制所有这些作用。淫羊藿次苷II可显著增强rBMSCs的成骨分化,但如果用L - NAME阻断iNOS的活性,则成骨分化标志物会随着iNOS和NO的减少而降低,这表明淫羊藿次苷II通过增强iNOS的活性和促进NO的生成来刺激成骨分化。

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