中文摘要：

摘要：目的：以小鼠骨髓间充质干细胞系D1细胞为研究对象，探讨Wnt／β-catenin信号通路介导的红景天苷诱导D1细胞向神经细胞的定向分化。方法：实验分为对照组（D／F12完全培养基）和红景天苷诱导组（100μg／mL＋D／F12完全培养基）．将细胞分别诱导12、24、48和72h后，采用细胞免疫荧光化学染色方法检测β-catenin和Gsk-3β的阳性细胞率。利用红景天苷分别诱导MSCsi，2，8，12，24，48和72h后，利用实时PCR技术检测Wnt／β-catenin信号通路的关键信号分子wnt3a、Axin2、Lrp6和Gsk-3β mRNA的表达；采用Westernblot方法分析D1细胞诱导12、24、48和72h后，β-catenin和Gsk-3β蛋白的表达；运用Wnt／β-catenin信号通路特异性阻断剂DKKl阻断Wnt／β-catenin信号通路，Westernblot方法分析红景天苷对β-catenin和NSE蛋白表达的影响。结果：红景天苷诱导24h时β-catenin的阳性率可达55．76％，与其他组和对照组比较差异具有统计学意义（P〈0．01），诱导24h后Gsk-3β的阳性率与其他时间和对照组比较差异有统计学意义（P〈0．05）。实时PCR检测结果显示，红景天苷诱导MSCs不同时间能促进Wnt／β-catenin信号通路中关键信号分子Wnt3a、Ax-in2、Lrp6和Gsk-3β mRNA的表达，诱导不同时间Wnt3a、Axin2、Lrp6和Gsk-3βmRNA的表达不尽相同。Westernblot结果表明，红景天苷诱导D1细胞12h和24h时β-catenin蛋白的表达明显上调，且与其他组比较差异具有统计学意义（P〈0．05）；随着作用时间的延长，Gsk-3β蛋白的表达增加且差异具有统计学意义（P〈0．05），阻断Wnt／β-catenin信号通路后，β-catenin和NSE蛋白的表达水平明显下调。结论：红景天苷能诱导D1细胞定向分化为神经元样细胞，红景天苷通过激活Wnt／β-catenin信号通路实现其诱导MSCs向神经细胞定向分化。

英文摘要：

Objective：This work was carried out to investigate the directed differentiation of MSCs into neural cells inWnt/β-catenin signaling pathway induced by salidroside （SD）, utilizing the mouse bone marrow-derived mesenchymal stem cell series D1 as the model. Methods：Two groups were designed,a control group （D/F12 complete medium） and a SD group （ 100 μg,/mL ＋ D/F12 complete medium）. These two groups were left to induction for 12,24,48 and 72 h and the positive rate of NSE, MAP2,β-Tubulin III and GFAP, as well as the expression of β-catenin and GSK-3β were detected by immunocytochemistry staining method. The real-time PCR results gave the expression of the critical signaling molecules in Wnt/β-catenin signaling pathway, such as wnt3a, Axin2, Lrp6 and Gsk-3β mRNA. The expression of β- catenin and Gsk-3β were analyzed according to Western blot method. Results：It was found that salidrosides can induce MSCs differentiate into neuron-like cells. In the case of SD group with the induction time of 24 h, the positive rate of β- catenin was 55.76% and a significant difference was observed compared with the control group （ P 〈 0.01 ）. Mean- while,the positive rate of Gsk-3β also exhibited significant difference when induced for a period of 24 and 48 h. Real- time PCR results indicated that all the signaling molecules, Wnt3a, Axin2, Lrp6, and Gsk-3β mRNA could be efficiently expressed in the SD groups at each time point. The only difference is that the extent of expression changed with the in- creasing induction time. From the Western blot, the expression of β-catenin protein and Gsk-313 gradually went up in the SD groups with the increasing time, which is significantly different from the control groups （ P 〈 0.05 ）. The expression of β-catenin and NSE protein, which was induced with salidroside, were significantly decreased while Wnt/β-catenin sig- nal pathway was blocked by DKK1. Conclusions ： Salidroside can induce the differentiation of MSCs into neuron-like cells and Wnt/β-c