College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, 450000, People's Republic of China.
College of Veterinary Medicine, Henan Agricultural University, Zhengzhou, 450000, People's Republic of China; Wuhu Overseas Students Pioneer Park, Wuhu, 241006, PR China.
Theriogenology. 2021 Jun;167:85-93. doi: 10.1016/j.theriogenology.2021.03.012. Epub 2021 Mar 19.
After parturition, bovine uterine stromal cells are often exposed to complex bacterial and viral stimuli owing to epithelial cell rupture, resulting in an inflammatory response. In this study, we used an in vitro model to study the response of bovine endometrial stromal cells to inflammatory mediators and the associated regulated microRNAs in response to lipopolysaccharide. Lipopolysaccharide (LPS) is a bacterial wall component in gram-negative bacteria that causes inflammation upon immune recognition, which is used to create in vitro inflammation models. Thus, we used high-throughput RNA sequencing to identify miRNAs that may have an anti-inflammatory role in the LPS-induced inflammatory response. Two groups of bovine uterine cells were treated with phosphate buffer saline (PBS) and LPS, respectively. Compared with the control (PBS) group, the LPS-treated group had 219 differentially expressed miRNAs, of which 113 were upregulated, and 106 were downregulated. Gene ontology enrichment analysis revealed that the target genes of differentially expressed miRNAs were significantly enriched in several activities, such as transferase activity, small molecule binding, and protein binding. Kyoto Encyclopedia of Genes and Genomes pathway analysis indicated that the target genes of differential miRNAs were significantly enriched in fluid shear stress and atherosclerosis, MAPK signaling pathway, TNF signaling pathway. By analyzing differentially expressed miRNAs, we found that miR-200c, miR-1247-3p, and let-7b are directly related to the inflammatory response. For instance, miR-200c target genes (MAP3K1, MAP4K3, MAPKAPK5, MAP3K8, MAP3K5) and let-7b target genes (CASP3, IL13, MAPK8, CXCL10) were significantly enriched in the MAPK and IL-17 signaling pathways, respectively. In summary, our research provides insight into the molecular mechanism underlying LPS-induced inflammation in vitro, which may unveil new targets for the treatment of endometritis.
分娩后,由于上皮细胞破裂,牛的子宫基质细胞经常暴露于复杂的细菌和病毒刺激下,导致炎症反应。在这项研究中,我们使用体外模型研究了牛子宫内膜基质细胞对炎症介质的反应以及对脂多糖的反应相关调节 microRNA。脂多糖(LPS)是革兰氏阴性菌细胞壁的组成部分,在免疫识别时会引起炎症,常用于创建体外炎症模型。因此,我们使用高通量 RNA 测序来鉴定在 LPS 诱导的炎症反应中可能具有抗炎作用的 microRNA。两组牛子宫细胞分别用磷酸盐缓冲盐水(PBS)和 LPS 处理。与对照组(PBS)相比,LPS 处理组有 219 个差异表达的 microRNA,其中 113 个上调,106 个下调。基因本体富集分析显示,差异表达 microRNA 的靶基因显著富集于几种活性中,如转移酶活性、小分子结合和蛋白质结合。京都基因与基因组百科全书通路分析表明,差异 microRNA 的靶基因显著富集于流体剪切力和动脉粥样硬化、MAPK 信号通路、TNF 信号通路。通过分析差异表达的 microRNA,我们发现 miR-200c、miR-1247-3p 和 let-7b 与炎症反应直接相关。例如,miR-200c 的靶基因(MAP3K1、MAP4K3、MAPKAPK5、MAP3K8、MAP3K5)和 let-7b 的靶基因(CASP3、IL13、MAPK8、CXCL10)分别显著富集于 MAPK 和 IL-17 信号通路中。总之,我们的研究提供了 LPS 诱导的体外炎症分子机制的见解,这可能为子宫内膜炎的治疗揭示新的靶点。