College of Veterinary Medicine, South China Agricultural University, Guangzhou, 510642, China.
Key Laboratory of Zoonosis Prevention and Control of Guangdong Province, South China Agricultural University, Guangzhou, 510642, China.
Vet Res. 2021 Aug 19;52(1):110. doi: 10.1186/s13567-021-00979-x.
This study aimed to explore the mutual regulation between chicken telomerase reverse transcriptase (chTERT) and the Wnt/β-catenin signalling pathway and its effects on cell growth and avian leukosis virus subgroup J (ALV-J) replication in LMH cells. First, LMH cells stably overexpressing the chTERT gene (LMH-chTERT cells) and corresponding control cells (LMH-NC cells) were successfully constructed with a lentiviral vector expression system. The results showed that chTERT upregulated the expression of β-catenin, Cyclin D1, TCF4 and c-Myc. chTERT expression level and telomerase activity were increased when cells were treated with LiCl. When the cells were treated with ICG001 or IWP-2, the activity of the Wnt/β-catenin signalling pathway was significantly inhibited, and chTERT expression and telomerase activity were also inhibited. However, when the β-catenin gene was knocked down by small interfering RNA (siRNA), the changes in chTERT expression and telomerase activity were consistent with those in cells treated with ICG001 or IWP-2. These results indicated that chTERT and the Wnt/β-catenin signalling pathway can be mutually regulated. Subsequently, we found that chTERT not only shortened the cell cycle to promote proliferation but also inhibited apoptosis by downregulating the expression of Caspase 3, Caspase 9 and BAX; upregulating BCL-2 and BCL-X expression; and promoting autophagy. Moreover, chTERT significantly enhanced the migration ability of LMH cells, upregulated the protein and mRNA expression of ALV-J and increased the virus titre. ALV-J replication promoted chTERT expression and telomerase activity.
本研究旨在探讨鸡端粒酶逆转录酶(chTERT)与 Wnt/β-catenin 信号通路之间的相互调控及其对 LMH 细胞中细胞生长和禽白血病病毒亚群 J(ALV-J)复制的影响。首先,我们使用慢病毒载体表达系统成功构建了稳定过表达 chTERT 基因的 LMH 细胞(LMH-chTERT 细胞)及其相应的对照细胞(LMH-NC 细胞)。结果表明,chTERT 上调了β-catenin、Cyclin D1、TCF4 和 c-Myc 的表达。用 LiCl 处理细胞时,chTERT 表达水平和端粒酶活性增加。当用 ICG001 或 IWP-2 处理细胞时,Wnt/β-catenin 信号通路的活性显著抑制,chTERT 表达和端粒酶活性也受到抑制。然而,当用小干扰 RNA(siRNA)敲低β-catenin 基因时,chTERT 表达和端粒酶活性的变化与用 ICG001 或 IWP-2 处理的细胞一致。这些结果表明,chTERT 和 Wnt/β-catenin 信号通路可以相互调节。随后,我们发现 chTERT 不仅通过下调 Caspase 3、Caspase 9 和 BAX 的表达、上调 BCL-2 和 BCL-X 的表达以及促进自噬来缩短细胞周期以促进增殖,还抑制凋亡。此外,chTERT 显著增强了 LMH 细胞的迁移能力,上调了 ALV-J 的蛋白和 mRNA 表达,并增加了病毒滴度。ALV-J 复制促进了 chTERT 表达和端粒酶活性。