Effect of forsythoside A on the transcriptional profile of bovine mammary epithelial cells challenged with lipoteichoic acid

被引:1
作者
Shen, Puxiu [1 ]
Yu, Jingcheng [1 ]
Long, Xiaochuan [2 ]
Huang, Xiankai [2 ]
Tong, Chao [1 ,3 ]
Wang, Xinzhuang [1 ]
机构
[1] Henan Agr Univ, Coll Vet Med, Zhengzhou 450046, Peoples R China
[2] Guizhou Univ, Xibei Community Serv Ctr, Coll Anim Sci, Phase 2,West Campus, Guiyang, Guizhou, Peoples R China
[3] Wushu Overseas Students Pioneer Pk, Wuhu, Peoples R China
关键词
differentially expressed genes; forsythoside; lipoteichoic acid; mastitis; RNA sequencing; CANCER; APOPTOSIS;
D O I
10.1111/rda.14265
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 is a common disease of the dairy cattle, which affects the development of the dairy industry and leads to huge economic losses. Forsythoside A (FTA) has anti-inflammatory, antioxidant, antiviral and anti-apoptotic effects. However, the therapeutic effect and molecular mechanism of FTA on dairy cow mastitis remain unclear. In this study, bovine mammary epithelial cells (BMECs) were stimulated with lipoteichoic acid (LTA), a key virulence factor of Staphylococcus aureus (S. aureus), to construct in vitro models, and then treated with FTA. Subsequently, the differentially expressed genes (DEGs) in different groups were determined by RNA sequencing (RNA-Seq) analysis. Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) were used to analyse the possible function of the DEGs, real-time quantitative PCR (RT-qPCR) was used to verify whether the expression levels of these DEGs were consistent with RNA-Seq results. The results showed that cell division cycle 20B (CDC20B), endothelial cell surface expressed chemotaxis and apoptosis regulator (ECSCR), complement factor H-related 5 (CFHR5) and phospholipase A2 group IVA (PLA2G4A) were down-regulated after FTA treatment. In contrast, Kruppel-like factor 15 (KLF15) and Metallothionein 1E (MT1E) were up-regulated. These DEGs are involved in processes such as apoptosis, inflammation and development of cancer. This study provides valuable insights into the transcriptome changes in BMECs after FTA treatment. Further analysis may help identify the underlying molecular mechanisms.
引用
收藏
页码:89 / 96
页数:8
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