AI Article Synopsis

  • Lipopolysaccharide (LPS) from Gram-negative bacteria is linked to mastitis and metritis in dairy cattle, causing inflammation in the endometrium and stimulating proliferation of endometrial epithelial cells.
  • A transcriptomic study identified 752 and 727 differentially expressed genes (DEGs) related to proliferation and apoptosis after exposing bovine endometrial epithelial cells to various concentrations of LPS.
  • The analysis revealed 116 potential transcription factors and highlighted key signaling pathways, showing that LPS significantly activates pro-inflammatory and cell proliferation pathways, which may explain its role in endometrial issues.

Article Abstract

Lipopolysaccharide (LPS) is a component of the outer membrane of Gram-negative bacteria involved in the pathogenic processes leading to mastitis and metritis in animals such as dairy cattle. LPS causes cell proliferation associated with endometrium inflammation. Former studies have demonstrated that LPS induces an intense stimulation of the proliferation of a pure population of bovine endometrial epithelial cells. In a follow-up transcriptomic study based on RNA-sequencing data obtained after 24 h exposure of primary bovine endometrial epithelial cells to 0, 2, and 8 μg/mL LPS, 752 and 727 differentially expressed genes (DEGs) were detected between the controls and LPS-treated samples that encode proteins known to be associated with either proliferation or apoptosis, respectively. The present bioinformatic analysis was performed to decipher the gene networks involved to obtain a deeper understanding of the mechanisms underlying the proliferative and apoptosis processes. Our findings have revealed 116 putative transcription factors (TFs) and the most significant number of interactions between these TFs and DEGs belong to , , , and . Moreover, our results provide novel insights into the early signaling and metabolic pathways in bovine endometrial epithelial cells associated with the innate immune response and cell proliferation to -LPS infection. The results further indicated that LPS challenge elicited a strong transcriptomic response, leading to potent activation of pro-inflammatory pathways that are associated with a marked endometrial cancer, Toll-like receptor, NFKβ, AKT, apoptosis, and MAPK signaling pathways. This effect may provide a mechanistic explanation for the relationship between LPS and cell proliferation.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778113PMC
http://dx.doi.org/10.3390/genes13122342DOI Listing

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