Department of Veterinary Medicine, China Agricultural University, Beijing, China.
Front Immunol. 2021 Sep 14;12:715098. doi: 10.3389/fimmu.2021.715098. eCollection 2021.
is one of the most important pathogens that cause clinical mastitis in dairy cattle worldwide and lead to severe economic losses. Antibiotics are often used to treat this inflammatory disease; however, antimicrobial resistance and environmental pollution cannot be ignored. Probiotic is the best alternative; however, its mechanisms of action to prevent mastitis remain unclear. Moreover, the role of probiotics in regulating mitophagy, a selective autophagy that maintains mitochondrial quality, needs to be explored. infection induced NOD-like receptor family member pyrin domain-containing protein 3 (NLRP3) inflammasome assembly, Caspase-1 activation, and apoptosis in MAC-T cells. Infection also resulted in mitochondrial damage and subsequent increase in reactive oxygen species (ROS) production. Moreover, inhibition of ROS release by scavenger N-acetyl-L-cysteine (NAC) abrogated the importance of ROS in NLRP3 assembly and apoptosis in MAC-T cells. Pretreatment with GR-1 (LGR-1), a probiotic, alleviated -induced NLRP3 inflammasome activation and apoptosis ROS inhibition. Besides, infection inhibited mitophagy while LGR-1 pretreatment augmented PINK1/Parkin-mediated mitophagy activation, which further blocked ROS generation. To explore the effect of LGR-1 , a mouse mastitis model was established. The results showed that LGR-1 pretreatment had preventive and protective effects on induced mastitis, and could reduce cytokines levels such as IL-1β and TNF-α. In accordance with the results , can inhibit mitophagy and activate NLRP3 inflammasome and apoptosis, while LGR-1 can weaken the effect of . Taken together, our data indicated that LGR-1 pretreatment induced PINK1/Parkin-mediated mitophagy that eliminated damaged mitochondria and reduced ROS production and NLRP3 inflammasome activation, which subsequently decreased -induced apoptosis. To conclude, our study suggests that therapeutic strategies aiming at the upregulation of mitophagy under -induced mastitis may preserve mitochondrial function and provide theoretical support for the application of probiotics in bovine mastitis.
是引起全世界奶牛临床乳腺炎的最重要病原体之一,导致严重的经济损失。抗生素常用于治疗这种炎症性疾病;然而,抗生素耐药性和环境污染不容忽视。益生菌是最好的替代品;然而,其预防乳腺炎的作用机制尚不清楚。此外,需要探索益生菌在调节自噬中的作用,自噬是一种维持线粒体质量的选择性自噬。 感染诱导 MAC-T 细胞中 NOD 样受体家族成员 pyrin 结构域包含蛋白 3 (NLRP3) 炎性体组装、Caspase-1 激活和细胞凋亡。感染还导致线粒体损伤,随后活性氧 (ROS) 产生增加。此外,通过清除剂 N-乙酰-L-半胱氨酸 (NAC) 抑制 ROS 释放可消除 ROS 在 MAC-T 细胞中 NLRP3 组装和凋亡中的重要性。用益生菌 GR-1 (LGR-1) 预处理可减轻 诱导的 NLRP3 炎性体激活和凋亡 ROS 抑制。此外, 感染抑制了线粒体自噬,而 LGR-1 预处理增强了 PINK1/Parkin 介导的线粒体自噬激活,进一步阻止了 ROS 的产生。为了探讨 LGR-1 的作用,建立了小鼠乳腺炎模型。结果表明,LGR-1 预处理对 诱导的乳腺炎具有预防和保护作用,可降低白细胞介素-1β和肿瘤坏死因子-α等细胞因子水平。与结果一致, 可以抑制线粒体自噬并激活 NLRP3 炎性体和细胞凋亡,而 LGR-1 可以减弱 的作用。综上所述,我们的数据表明,LGR-1 预处理诱导的 PINK1/Parkin 介导的线粒体自噬消除了受损的线粒体,减少了 ROS 的产生和 NLRP3 炎性体的激活,从而减少了 诱导的细胞凋亡。总之,我们的研究表明,针对乳腺炎下线粒体自噬上调的治疗策略可能有助于维持线粒体功能,并为益生菌在奶牛乳腺炎中的应用提供理论支持。