Department of Animal Anatomy and Physiology, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, Olsztyn, Poland.
Department of Plant Physiology, Genetics and Biotechnology, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, Olsztyn, Poland.
Biol Reprod. 2021 Jan 4;104(1):130-143. doi: 10.1093/biolre/ioaa200.
Female fertility depends greatly on the capacity of the uterus to recognize and eliminate microbial infections, a major reason of inflammation in the endometrium in many species. This study aimed to determine the in vitro effect of peroxisome proliferator-activated receptor gamma (PPARγ) ligands on the transcriptome genes expression and alternative splicing in the porcine endometrium in the mid-luteal phase of the estrous cycle during LPS-stimulated inflammation using RNA-seq technology. The endometrial slices were incubated in vitro in the presence of LPS and PPARγ agonists-PGJ2 or pioglitazone and antagonist-T0070907. We identified 222, 3, 4, and 62 differentially expressed genes after LPS, PGJ2, pioglitazone, or T0070907 treatment, respectively. In addition, we detected differentially alternative spliced events: after treatment with LPS-78, PGJ2-60, pioglitazone-52, or T0070907-134. These results should become a basis for further studies explaining the mechanism of PPARγ action in the reproductive system in pigs.
女性生育能力在很大程度上取决于子宫识别和消除微生物感染的能力,这也是许多物种子宫内膜炎的主要原因。本研究旨在使用 RNA-seq 技术确定过氧化物酶体增殖物激活受体γ (PPARγ) 配体在发情周期中期 LPS 刺激炎症期间对猪子宫内膜转录组基因表达和选择性剪接的体外影响。用 LPS 和 PPARγ 激动剂-PGJ2 或吡格列酮以及拮抗剂-T0070907 体外孵育子宫内膜切片。分别用 LPS、PGJ2、吡格列酮或 T0070907 处理后,我们鉴定出 222、3、4 和 62 个差异表达基因。此外,我们还检测到差异选择性剪接事件:用 LPS-78、PGJ2-60、吡格列酮-52 或 T0070907-134 处理后。这些结果应该成为进一步研究解释 PPARγ 在猪生殖系统中作用机制的基础。