Activation of PINK1-mediated mitophagy protects bovine mammary epithelial cells against lipopolysaccharide-induced mitochondrial and inflammatory damage in vitro

• Published in: Free radical biology & medicine Vol. 194; pp. 172 - 183
• Main Authors: Chang, Renxu, Tang, Yan, Jia, Hongdou, Dong, Zhihao, Gao, Shuang, Song, Qian, Dong, Hao, Xu, Qiushi, Jiang, Qianming, Loor, Juan J., Sun, Xudong, Xu, Chuang
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.2023
• Subjects: Animals; Autophagy; Bovine mammary epithelial cells; Cattle; Epithelial Cells - metabolism; Female; Inflammasomes - metabolism; Lipopolysaccharides - pharmacology; Mitochondria - metabolism; Mitochondrial damage; Mitophagy; NLR Family, Pyrin Domain-Containing 3 Protein - metabolism; NLRP3; PINK1; Protein Kinases - genetics; Protein Kinases - metabolism; Reactive Oxygen Species - metabolism; NLRP3; PINK1; Bovine mammary epithelial cells; Mitophagy; Mitochondrial damage
• ISSN: 0891-5849; 1873-4596; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2022.11.044

Increased metabolic stress during early lactation results in damage of mitochondria and inflammatory responses in bovine mammary epithelial cells, both of which could be aggravated by inhibition of mitophagy. PTEN-induced putative kinase 1 (PINK1)-mediated mitophagy is essential in the removal of damaged mitochondria and the regulation of inflammatory responses. The aim of the present study was to elucidate the role of PINK1-mediated mitophagy on mitochondrial damage and inflammatory responses in bovine mammary epithelial cells challenged with lipopolysaccharide (LPS). Exogenous LPS activated mitophagy and led to lower protein abundance of oxidative phosphorylation (OXPHOS) complexes (COI–V) and lower oxygen consumption rate (OCR) along with increased mitochondrial reactive oxygen species (Mito-ROS) content. These effects were also associated with increased protein abundance of Nucleotide-binding oligomerization domain-like receptor containing pyrin domain 3 (NLRP3) in a time-dependent manner. Pretreatment with 3-Methyladenine (3-MA) or knockdown of PINK1 aggravated the downregulation of COI–V protein abundance, the increase in Mito-ROS content, and the protein abundance of NLRP3, Cleaved-Caspase-1 and IL-1β induced by LPS. Overexpression of PINK1 activated mitophagy and alleviated LPS-induced NLRP3 inflammasome activation by reducing Mito-ROS production. Overall, the data suggested that PINK1-mediated mitophagy is a crucial anti-inflammatory mechanism that removes damaged mitochondria in bovine mammary epithelial cells experiencing an increased inflammatory load. •Exogenous LPS induced mitochondrial damage and inflammation in MAC-T cells.•Overexpression of PINK1 enhanced LPS-induced mitophagy in MAC-T cells.•PINK1-mediated mitophagy alleviated inflammation by remove damaged mitochondria.