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首页> 外文期刊>International journal of molecular medicine >Overexpression of heparan sulfate 6-O-sulfotransferase-2 enhances fibroblast growth factor-mediated chondrocyte growth and differentiation
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Overexpression of heparan sulfate 6-O-sulfotransferase-2 enhances fibroblast growth factor-mediated chondrocyte growth and differentiation

机译:硫酸乙酰肝素6-O-磺基转移酶-2的过表达增强成纤维细胞生长因子介导的软骨细胞的生长和分化

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In our previous study, we reported that heparan sulfate 6-O-sulfotransferase?2?(HS6ST2) plays an important role in the cartilage of patients with osteoarthritis and Kashin-Beck disease and that it regulates aggrecan?(Acan) metabolism and the viability of chondrocytes. However, its role in chondrocyte differentiation remains poorly understood. In the present study, we aimed to investigate the role of HS6ST2 in chondrocyte differentiation in?vitro using mouse prechondrocytic cells. We found that the overexpression or silencing of HS6ST2 significantly enhanced or abrogated the effects of fibroblast growth factor (FGF)?2 on chondrocyte growth, respectively. We found that the overexpression of HS6ST2 significantly induced the expression of Acan as well as the amount of total proteoglycans in the prechondrocytic cells in the presence of FGF?2, whereas the silencing of HS6ST2 caused the opposite effect. Furthermore, the expresssion of FGF?2?induced sex?determining region?Y?type high mobility group box protein?9?(SOX9), a major transcription factor for chondrocyte proliferation and differentiation, was also enhanced or blocked by HS6ST2 overexpression or HS6ST2 knockdown, respectively. Additionally, Wnt/β?catenin signaling, which inhibited chondrocyte proliferation and differentiation, was suppressed by HS6ST2. Taken together, these data suggest that HS6ST2 plays an important role in regulating chondrocyte growth and differentiation by modulating FGF?2 signaling, thus indicating that it may be a potential and valuable molecular target for the treatment of skeletal dysplasias, such as dwarfism.
机译:在我们以前的研究中,我们报道了硫酸乙酰肝素6-O-磺基转移酶β2?(HS6ST2)在骨关节炎和Kashin-Beck病患者的软骨中起重要作用,并且它调节聚集蛋白聚糖(Acan)的代谢和生存能力。软骨细胞。但是,其在软骨细胞分化中的作用仍然知之甚少。在本研究中,我们旨在研究HS6ST2在使用小鼠软骨细胞的体外软骨细胞分化中的作用。我们发现,HS6ST2的过表达或沉默分别显着增强或消除了成纤维细胞生长因子(FGF)?2对软骨细胞生长的影响。我们发现,在FGF?2存在的情况下,HS6ST2的过表达显着诱导了软骨细胞中Acan的表达以及总蛋白聚糖的量,而HS6ST2的沉默则产生了相反的作用。此外,HS6ST2过表达或HS6ST2也增强或阻断了FGF2诱导性决定区γY型高迁移率族框蛋白9(SOX9)的表达,这是软骨细胞增殖和分化的主要转录因子。分别击倒。此外,抑制软骨细胞增殖和分化的Wnt /β-catenin信号传导被HS6ST2抑制。综上所述,这些数据表明,HS6ST2通过调节FGF?2信号在调节软骨细胞的生长和分化中起着重要作用,因此表明它可能是治疗骨骼发育不良(例如侏儒症)的潜在且有价值的分子靶标。

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