Key Laboratory of Animal Disease and Human Health of Sichuan Province, College of Veterinary Medicine, Sichuan Agricultural University, Chengdu 611130, China.
Int J Mol Sci. 2023 Jul 11;24(14):11331. doi: 10.3390/ijms241411331.
Yaks are often subject to long-term starvation and a high prevalence of respiratory diseases and mortality in the withered season, yet the mechanisms that cause this remain unclear. Research has demonstrated that β-hydroxybutyrate (BHB) plays a significant role in regulating the immune system. Hence, we hypothesize that the low glucose and high BHB condition induced by severe starvation might have an effect on the pro-inflammatory response of the alveolar macrophages (AMs) in yaks. To validate our hypothesis, we isolated and identified primary AMs from freshly slaughtered yaks and cultured them in a medium with 5.5 mM of glucose or 2.8 mM of glucose plus 1-4 mM of BHB. Utilizing a real-time quantitative polymerase chain reaction (RT-qPCR), immunoblot assay, and enzyme-linked immunosorbent assay (ELISA), we evaluated the gene and protein expression levels of GPR109A (G-protein-coupled receptor 109A), NF-κB p65, p38, and PPARγ and the concentrations of pro-inflammatory cytokines interleukin (IL)-1β and IL-6 and tumor necrosis factor (TNF)-α in the supernatant. The results demonstrated that AMs exposed to low glucose plus BHB had significantly higher levels of IL-1β, IL-6, and TNF-α ( < 0.05) and higher activity of the GPR109A/NF-κB signaling pathway. A pretreatment of either pertussis toxin (PTX, inhibitor of GPR109A) or pyrrolidinedithiocarbamic (PDTC, inhibitor of NF-κB p65) was effective in preventing the elevated secretion of pro-inflammatory cytokines induced by low glucose plus BHB ( < 0.05). These results indicated that the low glucose plus BHB condition would induce an enhanced pro-inflammatory response through the activation of the GPR109A/NF-κB signaling pathway in primary yak AMs, which is probably the reason why yaks experience a higher rate of respiratory diseases and mortality. This study will offer new insight into the prevention and treatment of bovine respiratory diseases.
牦牛在枯水季节经常遭受长期饥饿和高呼吸疾病发生率和死亡率的影响,但导致这种情况的机制尚不清楚。研究表明,β-羟丁酸(BHB)在调节免疫系统方面发挥着重要作用。因此,我们假设严重饥饿引起的低血糖和高 BHB 条件可能对牦牛肺泡巨噬细胞(AMs)的促炎反应产生影响。为了验证我们的假设,我们从刚宰杀的牦牛中分离并鉴定了原代 AMs,并在含有 5.5mM 葡萄糖或 2.8mM 葡萄糖加 1-4mM BHB 的培养基中培养它们。利用实时定量聚合酶链反应(RT-qPCR)、免疫印迹分析和酶联免疫吸附试验(ELISA),我们评估了 GPR109A(G 蛋白偶联受体 109A)、NF-κB p65、p38 和 PPARγ 的基因和蛋白表达水平以及上清液中促炎细胞因子白细胞介素(IL)-1β和 IL-6 和肿瘤坏死因子(TNF)-α的浓度。结果表明,暴露于低糖加 BHB 的 AMs 具有显著更高水平的 IL-1β、IL-6 和 TNF-α(<0.05)和更高活性的 GPR109A/NF-κB 信号通路。普洛立定毒素(PTX,GPR109A 抑制剂)或吡咯烷二硫代氨基甲酸盐(PDTC,NF-κB p65 抑制剂)的预处理可有效防止低糖加 BHB 诱导的促炎细胞因子的升高分泌(<0.05)。这些结果表明,低葡萄糖加 BHB 条件通过激活原代牦牛 AMs 中的 GPR109A/NF-κB 信号通路,会诱导增强的促炎反应,这可能是牦牛呼吸疾病和死亡率较高的原因。本研究将为牛呼吸疾病的预防和治疗提供新的见解。