College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Jiangsu Key Laboratory of Sericutural Biology and Biotechnology, School of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu 212018, China.
Mol Immunol. 2020 Nov;127:157-163. doi: 10.1016/j.molimm.2020.09.011. Epub 2020 Sep 25.
In the perinatal period of dairy cows, negative energy balance (NEB) is likely to occur, which increases the level of non-esterified fatty acids (NEFA) in the follicular fluid, hinders the proliferation of granulosa cells (GCs), and thus endangers the development of oocytes and the fecundity of dairy cows. We found that there were oxidative stress and inflammatory response in the serum of cows with perinatal ketosis. Whether the oxidative stress induced by NEFA is involved in the pyroptosis and inflammation of GCs remains unclear. After NEFA treatment, the expression of NLRP3 and caspase-1 and the release of inflammatory cytokines IL-1β were increased in a dose-dependent manner, indicating that NEFA may contribute to pyroptosis. Besides, NEFA stimulation induced oxidative stress, resulting in the phosphorylation of NF-κB, and increased the production of interleukin (IL)-6 and nitric oxide (NO), indicating that NEFA may induce inflammation in GCs. However, the NEFA-mediated effects were observably reversed when the GCs were pre-treated with antioxidant and radical scavenger, N-acetylcysteine (NAC). Taken together, our results reveal that NEFA can induce pyroptosis and inflammation through NLRP3 inflammasome and TLR4/NF-κB pathway, respectively, and NAC can alleviate these conditions.
在奶牛围产期,可能会发生负氮平衡(NEB),这会增加卵泡液中的非酯化脂肪酸(NEFA)水平,抑制颗粒细胞(GCs)的增殖,从而危害卵母细胞的发育和奶牛的繁殖力。我们发现,患有围产期酮病的奶牛的血清中存在氧化应激和炎症反应。NEFA 诱导的氧化应激是否参与 GCs 的细胞焦亡和炎症仍不清楚。经 NEFA 处理后,NLRP3 和半胱天冬酶-1 的表达以及炎性细胞因子 IL-1β 的释放呈剂量依赖性增加,表明 NEFA 可能导致细胞焦亡。此外,NEFA 刺激诱导氧化应激,导致 NF-κB 磷酸化,并增加白细胞介素(IL)-6 和一氧化氮(NO)的产生,表明 NEFA 可能导致 GCs 炎症。然而,当 GCs 用抗氧化剂和自由基清除剂 N-乙酰半胱氨酸(NAC)预处理时,NEFA 介导的作用明显逆转。综上所述,我们的研究结果表明,NEFA 可以通过 NLRP3 炎性小体和 TLR4/NF-κB 途径分别诱导细胞焦亡和炎症,而 NAC 可以减轻这些情况。