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首页> 外文期刊>The international journal of biochemistry and cell biology >YAP1 negatively regulates chondrocyte differentiation partly by activating the beta-catenin signaling pathway
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YAP1 negatively regulates chondrocyte differentiation partly by activating the beta-catenin signaling pathway

机译:YAP1通过激活β-catenin信号传导途径部分地对细胞分化进行负调节细胞分化

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摘要

YAP1 (Yes-associated protein 1) transcriptional coactivator is a downstream gene of the Hippo signaling pathway, which controls cell proliferation and differentiation. YAP1 plays a significant role in the regulation of cartilage and bone development. However, the molecular mechanism by which YAP1 regulates chondrocyte differentiation remains to be elucidated. Immunofluorescent staining was used to visualize the localization of YAP1 expression in the mouse chondroprogenitor ATDC5 cell line. ATDC5 cells with lentivirus-vector-mediated YAP1 overexpression and knockdown were established. The differentiation abilities were examined by real-time quantitative PCR and two staining methods The expression levels of sex-determining region Y-type high mobility group box protein (SOX9) and key proteins in the Wnt/beta-catenin pathway were analyzed by Western blot. The Dickkopf-1 (Dkk1) and small interfering RNA (siRNA) of beta-catenin were used for further study. The YAP1 protein was mainly expressed in the nucleus of ATDC5 cells. YAP1 overexpression enhanced chondrocyte proliferation but inhibited chondrocyte differentiation, which were contrary to the findings of the YAP1-knockdown group. Moreover, YAP1 overexpression activated Wnt/beta-catenin signaling pathway. Treatment with exogenous DKK1 and beta-catenin siRNA partially recaptured the effects of YAP1 overexpression on ATDC5 cell differentiation. Taken together, our study suggested that YAP1 attenuated ATDC5 cell chondrogenic and hypertrophic differentiation. We also demonstrated that YAP1 exerted its effect on the chondrocyte differentiation by activating the Wnt/beta-catenin signaling pathway.
机译:YAP1(yes-相关的蛋白质1)转录共觉器是河马信号通路的下游基因,其控制细胞增殖和分化。 YAP1在调节软骨和骨骼发育中起着重要作用。然而,YAP1调节软骨细胞分化的分子机制仍有待阐明。使用免疫荧光染色来可视化小鼠软糖氢催化剂ATDC5细胞中YAP1表达的定位。 ATDC5与慢病毒 - 载体介导的YAP1过表达和敲低的细胞。通过实时定量PCR检测分化能力,并通过Western印迹分析了两种染色方法,通过WebR / Beta-catenin途径中的性别测定区域Y型高迁移率组蛋白(SOX9)和关键蛋白质的表达水平。 β-catenin的Dickkopf-1(DKK1)和小干扰RNA(siRNA)用于进一步研究。 YAP1蛋白主要在ATDC5细胞的细胞核中表达。 YAP1过表达增强的软骨细胞增殖,但抑制软骨细胞分化,这与YAP1敲低局部的结果相反。此外,YAP1过表达活化的WNT /β-连环蛋白信号通路。用外源性DKK1和β-连环蛋白siRNA治疗部分重新覆盖YAP1过表达对ATDC5细胞分化的影响。我们的研究表明,YAP1减弱了ATDC5细胞软骨内和肥厚分化。我们还证明了YAP1通过激活WNT /β-连环蛋白信号通路来施加对软骨细胞分化的影响。

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