Methionine and arginine supplementation alter inflammatory and oxidative stress responses during lipopolysaccharide challenge in bovine mammary epithelial cells in vitro

被引:49
|
作者
Dai, H. [1 ,2 ,3 ]
Coleman, D. N. [2 ,3 ]
Hu, L. [2 ,3 ,4 ]
Martinez-Cortes, I [2 ,3 ,5 ]
Wang, M. [4 ]
Parys, C. [6 ]
Shen, X. [1 ]
Loor, J. J. [2 ,3 ]
机构
[1] Nanjing Agr Univ, Coll Vet Med, Nanjing 210095, Jiangsu, Peoples R China
[2] Univ Illinois, Dept Anim Sci, 328 Mumford Hall, Urbana, IL 61801 USA
[3] Univ Illinois, Div Nutr Sci, Urbana, IL 61801 USA
[4] Yangzhou Univ, Coll Anim Sci & Technol, Yangzhou 225009, Jiangsu, Peoples R China
[5] UAM Xochimilco, Agr & Anim Prod Dept, Mexico City 04960, DF, Mexico
[6] Evonik Nutr & Care GmbH, D-63457 Hanau, Germany
关键词
amino acids; immune response; mammary epithelial cell; mastitis; NITRIC-OXIDE SYNTHASE; IMMUNE-RESPONSES; HEME OXYGENASE-1; AMINO-ACIDS; DAIRY-COWS; IMMUNOMETABOLIC STATUS; MACROPHAGES; GLUTATHIONE; METABOLISM; INDUCTION;
D O I
10.3168/jds.2019-16631
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Mastitis, inflammation of the udder, is one of the most common diseases hampering milk yield of dairy cows. Methionine (Met) and arginine (Arg) are key nutrients with potential to regulate inflammation and oxidative stress. The aim of this study was to evaluate the effect of increased supply of Met and Arg on mRNA, and protein abundance associated with innate immune response and redox balance during lipopolysaccharide (LPS) stimulation in primary bovine mammary epithelial cells (BMEC). Primary BMEC (n = 4 replicates per treatment) were pre-incubated for 12 h in media with the following amino acid combinations: ideal profile of amino acids (control; Con), increased Met supply (incMet), increased Arg supply (incArg), and increased supply of Met and Arg (incMetArg). Subsequently, cells were challenged with or without LPS (1 mu g/mL) and incubated for 6 h. Data were analyzed as a 2 x 2 x 2 factorial using the MIXED procedure of SAS 9.4 (SAS Institute Inc., Cary, NC). The downregulation of SLC36A1 and SLC7A1 mRNA abundance induced by LPS was attenuated in the incArg cultures. Although challenge with LPS led to lower abundance of proteins related to the antioxidant response (NFE2L2, NQO1, GPX1), lower levels of ATG7, and lower mRNA abundance of GPX3, we found little effect in cultures with incMet or incArg. Cultures with incMet, incArg, or incMetArg led to attenuation of the upregulation of SOD2 and NOS2 induced by LPS. Abundance of phosphorylated p65 (RELA) was greater after LPS stimulation, but the response was attenuated in cultures with incMet. The greater ratio of pRELA to total RELA. in responses to LPS was also attenuated in cultures with incMetArg. The greater mRNA abundance of the proinflammatory cytokine IL1B induced by LPS was attenuated in cultures with incMet, and the same trend induced by LPS on CXCL2 was also alleviated in cultures with incArg. Overall, the data suggest that greater supply of Met and Arg alleviated the proinflammatory responses triggered by LPS through controlling the abundance of proinflammatory cytokines and chemokines and activity of NF-kappa B. Little benefit on oxidative stress induced by LPS challenge in BMEC was detected with greater supply of Met and Arg.
引用
收藏
页码:676 / 689
页数:14
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