College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
College of Animal Science and Technology, Nanjing Agricultural University, Nanjing 210095, China.
Ecotoxicol Environ Saf. 2023 May;256:114889. doi: 10.1016/j.ecoenv.2023.114889. Epub 2023 Apr 18.
Heat stress (HS) triggers mammary gland degradation, accompanied by apoptosis and autophagy in bovine mammary epithelial cells, negatively affecting milk performance and mammary gland health. Ferroptosis is iron-mediated regulated cell death caused by over production of lipid peroxides, however, the relationship between ferroptosis and HS in bovine mammary epithelial cells has not been clarified. Methionine (Met) plays a notable role in alleviating HS affecting the mammary glands in dairy cows, but the underlying mechanisms require further exploration. Therefore, we evaluated the regulatory effect and mechanism of Met in alleviating HS-induced ferroptosis by using bovine mammary epithelial cell line (MAC-T) as an in vitro model. The results showed that Met improved cell vitality, restored mitochondrial function; reduced the content of various reactive oxygen species (ROS), especially hydrogen peroxide (HO) and superoxide anion (O-); had positive effects on antioxidant enzyme activity, namely glutathione peroxidase (GSH-Px) and superoxide dismutase (SOD). More importantly, Met reduced labile iron protein (LIP) levels; increased iron storage and simultaneously decreased the levels of lipid reactive oxygen species (lipid ROS) and malondialdehyde (MDA), which all caused by HS in MAC-T. Mechanistically, Met increased the protein expression levels of glutathione peroxidase 4 (GPX4), solute carrier family 7, member 11 (SLC7A11) and ferritin heavy chain 1 (FTH1) by activating nuclear factor E2-related factor 2 (Nrf2) expression. Additionally, the protection effect of Met was cut off in MAC-T cells after interference with Nrf2, manifesting in decresing the protein expression levels of GPX4, SLC7A11 and FTH1,and increasing the levels of LIP and lipid ROS. Our findings indicate that Met eases HS-induced ferroptosis in MAC-T through the Nrf2 pathway, revealing that Met produces a marked effect on easing HS-induced bovine mammary gland injury in dairy cows.
热应激 (HS) 会引发乳腺退化,伴随着牛乳腺上皮细胞的细胞凋亡和自噬,从而对产奶性能和乳腺健康产生负面影响。铁死亡是由脂质过氧化物过度产生引起的铁介导的调节性细胞死亡,然而,铁死亡与牛乳腺上皮细胞中的 HS 之间的关系尚未阐明。蛋氨酸 (Met) 在缓解热应激对奶牛乳腺的影响方面发挥着显著作用,但潜在机制仍需进一步探索。因此,我们使用牛乳腺上皮细胞系 (MAC-T) 作为体外模型,评估了 Met 缓解 HS 诱导的铁死亡的调节作用和机制。结果表明,Met 提高了细胞活力,恢复了线粒体功能;降低了各种活性氧 (ROS) 的含量,特别是过氧化氢 (HO) 和超氧阴离子 (O-);对谷胱甘肽过氧化物酶 (GSH-Px) 和超氧化物歧化酶 (SOD) 等抗氧化酶活性有积极影响。更重要的是,Met 降低了不稳定铁蛋白 (LIP) 的水平;增加铁储存,同时降低脂质活性氧 (lipid ROS) 和丙二醛 (MDA) 的水平,这些都是由 MAC-T 中的 HS 引起的。在机制上,Met 通过激活核因子 E2 相关因子 2 (Nrf2) 的表达,增加了谷胱甘肽过氧化物酶 4 (GPX4)、溶质载体家族 7 成员 11 (SLC7A11) 和铁蛋白重链 1 (FTH1) 的蛋白表达水平。此外,在 MAC-T 细胞中干扰 Nrf2 后,Met 的保护作用被阻断,表现为 GPX4、SLC7A11 和 FTH1 的蛋白表达水平降低,LIP 和脂质 ROS 的水平增加。我们的研究结果表明,Met 通过 Nrf2 通路缓解了 MAC-T 中的 HS 诱导的铁死亡,表明 Met 对缓解奶牛热应激引起的奶牛乳腺损伤具有显著作用。