Transcriptome Analysis Reveals That NEFA and β-Hydroxybutyrate Induce Oxidative Stress and Inflammatory Response in Bovine Mammary Epithelial Cells.
Chengmin LiJunpeng HuangXiangxing ChenYexiao YanLian LiWeiguo ZhaoPublished in: Metabolites (2022)
Non-esterified fatty acids (NEFA) and β-hydroxybutyrate (BHBA) are the metabolites of fat mobilization initiated by negative energy balance (NEB) during the perinatal period in dairy cows, which have an adverse effect on cell physiology of various bovine cell types. The aim of this study was to explore the biological roles of NEFA and BHBA on provoking oxidative stress and inflammatory responses in bovine mammary epithelial cells (BMECs). RNA sequencing analysis showed that there are 1343, 48, and 1725 significantly differentially expressed genes (DEGs) in BMECs treated with NEFA, BHBA and their combination. GO functional analysis revealed that the DEGs were significantly enriched in "response to oxidative stress" and "inflammatory response". Further study demonstrated that NEFA and BHBA elevated the malondialdehyde (MDA) and reactive oxygen species (ROS) accumulation and reduced the total superoxide dismutase (T-SOD) and glutathione peroxidase (GSH-Px) activity to cause oxidative stress. In addition, expression of inflammatory markers (NO, TNF-α, IL-6, and IL-1β) were increased after NEFA and BHBA stimulation. Mechanistically, our data showed that NEFA and BHBA activated the MAPK signaling pathway. Collectively, our results indicate that NEFA and BHBA induce oxidative stress and inflammatory response probably via the MAPK signaling pathway in BMECs.
Keyphrases
- oxidative stress
- inflammatory response
- signaling pathway
- induced apoptosis
- single cell
- dna damage
- reactive oxygen species
- diabetic rats
- ischemia reperfusion injury
- pi k akt
- lipopolysaccharide induced
- fatty acid
- dairy cows
- epithelial mesenchymal transition
- pregnant women
- hydrogen peroxide
- rheumatoid arthritis
- adipose tissue
- gene expression
- stem cells
- nitric oxide
- emergency department
- genome wide
- dna methylation
- mesenchymal stem cells
- heat shock
- big data
- data analysis
- cell cycle arrest