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Iksan526 Rice Callus Extract Induces Dedifferentiation of Rabbit Articular Chondrocytes via ERK1/2 and PI-3K/Akt Pathways

机译:IKSAN526稻愈伤组织提取物通过ERK1 / 2和PI-3K / AKT途径诱导兔关节软骨细胞的去分化

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The resveratrol-enriched transgenic rice line Iksan526 (IS526), first developed by the Rural Development Administration of Korea using genetic engineering techniques, shows beneficial health effects in mitigating metabolic syndrome and obesity. However, the effects of IS526 on the differentiation of chondrocytes and the underlying mechanism have not been investigated in detail. In this study, the effects and cellular regulatory mechanisms of IS526 on rabbit articular chondrocytes were examined. Following IS526 callus extract treatment, the expression levels of differentiation-related proteins were detected via western blotting, Alcian blue staining and immune-luorescence staining. IS526 decreased the type II collagen and proteoglycan levels in dose- and time-dependent manners. We further analyzed the effects of IS526 on skeleton genesis in zebrafish larvae using Alcian blue staining, which showed a reduction in cartilage formation along with increased production of matrix metalloproteinase (MMP)-13. IS526 also increased the phosphorylation of ERK1/2 and p38 kinase but inhibited the phosphorylation of Akt. Pharmacological inhibition of MMP-13 blocked the IS526-induced decrease in type II collagen levels. Inhibition of p38 kinase or PI-3K/Akt with SB203580 and LY294002 enhanced the suppression of type II collagen, but the blockage of ERK-1/2 by PD98059 rescued IS526-induced dedifferentiation. These results suggested that IS526 regulates type II collagen and MMP-13 expression via the ERK1/2 and PI-3K/Akt pathways in rabbit articular chondrocytes.
机译:富含白藜芦醇富含的转基因稻米Iksan526(IS526)首先由韩国农村发展管理使用基因工程技术开发,表明了缓解代谢综合征和肥胖症的有益健康影响。然而,尚未详细研究了IS526对软骨细胞和潜在机制的分化的影响。在该研究中,研究了IS526对兔关节软骨细胞的影响和细胞调节机制。在IS526愈伤组织提取物处理之后,通过蛋白质印迹,Alcian蓝染色和免疫旋转染色来检测分化相关蛋白的表达水平。 IS526以剂量和时间依赖的方式降低II型胶原蛋白和蛋白多糖水平。我们进一步分析了IS526对斑马鱼幼虫在斑马鱼幼虫的骨骼创世纪的影响,SALCian蓝染色显示软骨形成的降低以及基质金属蛋白酶(MMP)-13的增加。 IS526还增加了ERK1 / 2和P38激酶的磷酸化,但抑制AKT的磷酸化。 MMP-13的药理抑制阻断II型胶原蛋白水平的IS526诱导的降低。抑制P38激酶或PI-3K / AKT,具有SB203580和LY294002增强了II型胶原蛋白的抑制,但通过PD98059堵塞ERK-1/2的堵塞是526诱导的去分化。这些结果表明,IS526通过兔关节软骨细胞中的ERK1 / 2和PI-3K / AKT途径调节II型胶原蛋白和MMP-13表达。

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