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Activation of cannabinoid receptor type 2-induced osteogenic differentiation involves autophagy induction and p62-mediated Nrf2 deactivation

机译:大麻素2型受体诱导的成骨分化的激活涉及自噬诱导和p62介导的Nrf2失活

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摘要

Alterations in CNR2, autophagy molecules, and Nrf2 during osteogenic differentiation in vitro To stimulate osteogenic differentiation, hFOB 1.19 cells were transferred from 34 °C to 39 °C, and cultured for indicated periods. ALP activities of hFOB 1.19 cells were determined via a commercial kit. The expression levels of osteopontin and osteocalcin, two osteogenic markers, were analyzed with real-time PCR. Cell mineralization was determined with Alizarin red staining. mRNA expression levels of CNR2 and GAPDH were determined with RT-PCR. - Protein levels of CNR2, LC3, beclin 1, p62 and Nrf2 (nuclear and cytoplasmic) were determined with western blotting, and normalized to that of GAPDH or laminB. Symbols*, ** and *** indicated a value
机译:体外成骨分化过程中CNR2,自噬分子和Nrf2的变化为了刺激成骨分化,将hFOB 1.19细胞从34°C转移到39°C,并培养指定的时间。通过商业试剂盒测定hFOB 1.19细胞的ALP活性。用实时荧光定量PCR分析了两种成骨性标志物骨桥蛋白和骨钙素的表达水平。用茜素红染色测定细胞矿化。用RT-PCR测定CNR2和GAPDH的mRNA表达水平。 -用蛋白质印迹法测定CNR2,LC3,beclin 1,p62和Nrf2(核和细胞质)的蛋白质水平,并将其标准化为GAPDH或laminB的蛋白质水平。符号*,**和***表示一个值

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