Key Laboratory of Animal Disease and Human Health of Sichuan Province, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.
Chengdu Customs of the People's Republic of China, Chengdu, 610095, Sichuan, China.
BMC Vet Res. 2022 Aug 11;18(1):307. doi: 10.1186/s12917-022-03395-1.
Aside respiratory diseases, beef cattle may also suffer from serious kidney diseases after transportation. Hyperglycemia and gram-negative bacterial infection may be the main reasons why bovine is prone to severe kidney disease during transportation stress, however, the precise mechanism is still unclear. The purpose of the current study is to explore whether the combined treatment of high glucose (HG) and lipopolysaccharide (LPS) could induce madin-darby bovine kidney (MDBK) cells injury and autophagy, as well as investigate the potential molecular mechanisms involved.
As we discovered, the combined effect of HG and LPS decreased MDBK cells viability. And, HG and LPS combination also induced autophagy in MDBK cells, which was characterized by increasing the expression of LC3-II/I and Beclin1 and decreasing p62 expression. LC3 fluorescence signal formation was also significantly increased by HG and LPS combination treatment. Furthermore, we measured whether the mammalian target of rapamycin (mTOR) and the Notch3 signaling pathways were involved in HG and LPS-induced autophagy. The results showed that the combination of HG and LPS significantly increased the protein expression of Notch3 and decreased protein expression of p-mTOR, indicating that Notch3 and mTOR signaling pathways were activated. However, co-treatment with the Notch3 inhibitor (DAPT) could reverse the induction of autophagy, and increased the protein expression of p-mTOR.
This study demonstrated that the combination effect of HG and LPS could induce autophagy in MDBK cells, and the Notch3/mTOR signaling pathway was involved in HG and LPS-induced autophagy.
除了呼吸道疾病外,肉牛在运输后也可能患上严重的肾病。高血糖和革兰氏阴性菌感染可能是牛在运输应激时易发生严重肾病的主要原因,但具体机制尚不清楚。本研究旨在探讨高葡萄糖(HG)和脂多糖(LPS)联合处理是否会诱导牛肾细胞(MDBK)损伤和自噬,并探讨潜在的分子机制。
我们发现,HG 和 LPS 的联合作用降低了 MDBK 细胞活力。此外,HG 和 LPS 联合还诱导了 MDBK 细胞自噬,其特征是 LC3-II/I 和 Beclin1 的表达增加,p62 的表达减少。HG 和 LPS 联合处理也显著增加了 LC3 荧光信号的形成。此外,我们还测量了哺乳动物雷帕霉素靶蛋白(mTOR)和 Notch3 信号通路是否参与了 HG 和 LPS 诱导的自噬。结果表明,HG 和 LPS 的联合显著增加了 Notch3 的蛋白表达,降低了 p-mTOR 的蛋白表达,表明 Notch3 和 mTOR 信号通路被激活。然而,Notch3 抑制剂(DAPT)的共同处理可以逆转自噬的诱导,并增加 p-mTOR 的蛋白表达。
本研究表明,HG 和 LPS 的联合作用可诱导 MDBK 细胞自噬,Notch3/mTOR 信号通路参与了 HG 和 LPS 诱导的自噬。