College of Animal Science and Technology, Henan University of Science and Technology, Luoyang,471023, China.
Animal Husbandry and Veterinary Research Institute of Qingdao, 266000,Qingdao, China.
Pol J Vet Sci. 2020 Sep;23(3):359-372. doi: 10.24425/pjvs.2020.133653.
Telomerase reverse transcriptase (TERT) vectors were transfected into bone marrow mesen- chymal stem cells (BMSCs) which were then cultured and selected to establish TERT-BMSC cell lines whilst sequencing BMSCs and TERT-BMSCs via transcriptome in this study to explore their regulatory mechanism and effect on osteogenic differentiation after TERT ectopic expres- sion in sheep BMSCs. After sequencing and analysing differential genes, PI3K/Akt signalling pathway related to osteogenic differentiation was investigated. Western blot was used before and after applying the PI3K/Akt signalling pathway inhibitor LY294002 to detect protein expression levels of AKT and p-AKT. On the twenty-first day of osteogenic differentiation, RT-qPCR and Western blot were used to detect mRNA and protein expression levels of RUNX2 and OPN and alizarin red staining was utilised to analyse calcium salt deposition. Results showed that pro- tein expression levels of AKT and p-AKT were significantly up-regulated, mRNA and protein expression levels of RUNX2 and OPN increased and calcium salt deposition increased after ectopic expression of TERT. After applying LY294002, the protein expression of AKT and p-AKT was down-regulated, mRNA and protein expression levels of RUNX2 and OPN were reduced and calcium salt deposition was reduced. These results confirmed the stable integration and expression of the exogenous TERT gene in BMSCs to promote the differentiation of BMSC osteoblasts, which may be mediated by the PI3K/Akt signalling pathway.
端粒酶逆转录酶(TERT)载体被转染到骨髓间充质干细胞(BMSCs)中,然后进行培养和选择,以建立 TERT-BMSC 细胞系,同时通过转录组对 BMSCs 和 TERT-BMSC 进行测序,以探索其在绵羊 BMSCs 中 TERT 异位表达后对成骨分化的调节机制和影响。测序和分析差异基因后,研究了与成骨分化相关的 PI3K/Akt 信号通路。在应用 PI3K/Akt 信号通路抑制剂 LY294002 前后,使用 Western blot 检测 AKT 和 p-AKT 的蛋白表达水平。在成骨分化的第二十一天,使用 RT-qPCR 和 Western blot 检测 RUNX2 和 OPN 的 mRNA 和蛋白表达水平,并使用茜素红染色分析钙盐沉积。结果表明,TERT 异位表达后 AKT 和 p-AKT 的蛋白表达水平显著上调,RUNX2 和 OPN 的 mRNA 和蛋白表达水平增加,钙盐沉积增加。应用 LY294002 后,AKT 和 p-AKT 的蛋白表达下调,RUNX2 和 OPN 的 mRNA 和蛋白表达水平降低,钙盐沉积减少。这些结果证实了外源性 TERT 基因在 BMSCs 中的稳定整合和表达,促进了 BMSC 成骨细胞的分化,这可能是由 PI3K/Akt 信号通路介导的。