Mierzejewski Karol, Gerwel Zuzanna, Kurzyńska Aleksandra, Golubska Monika, Bogacka Iwona
Department of Animal Anatomy and Physiology, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, 10-719, Olsztyn, Poland.
Department of Animal Anatomy and Physiology, Faculty of Biology and Biotechnology, University of Warmia and Mazury in Olsztyn, 10-719, Olsztyn, Poland.
Theriogenology. 2023 Jun;203:69-81. doi: 10.1016/j.theriogenology.2023.03.003. Epub 2023 Mar 14.
The corpus luteum (CL) is a temporary endocrine structure in the female ovaries that develops cyclically in mature females during luteinization. This study aimed to determine the in vitro effects of peroxisome proliferator-activated receptor gamma (PPARγ) ligands on the transcriptomic profile of the porcine CL in the mid- and late-luteal phase of the estrous cycle using RNA-seq technology. The CL slices were incubated in the presence of PPARγ agonist - pioglitazone or antagonist - T0070907. We identified 40 differentially expressed genes after treatment with pioglitazone and 40 after treatment with T0070907 in the mid-luteal phase as well as 26 after pioglitazone and 29 after T0070907 treatment in the late-luteal phase of the estrous cycle. In addition, we detected differences in gene expression between the mid- and late-luteal phase without treatment (409 differentially expressed genes). This study revealed a number of novel candidate genes that may play a role in controlling the function of CL by regulating signaling pathways related to ovarian steroidogenesis, metabolic processes, cell differentiation, apoptosis, and immune responses. These findings become a basis for further studies to explain the mechanism of PPARγ action in the reproductive system.
黄体(CL)是雌性卵巢中的一种临时性内分泌结构,在成熟雌性动物的黄体化过程中呈周期性发育。本研究旨在利用RNA测序技术,确定过氧化物酶体增殖物激活受体γ(PPARγ)配体对发情周期中、后期猪黄体转录组图谱的体外影响。将黄体切片在PPARγ激动剂——吡格列酮或拮抗剂——T0070907存在的情况下进行孵育。我们发现在发情周期的中期,用吡格列酮处理后有40个差异表达基因,用T0070907处理后有40个;在发情周期的后期,用吡格列酮处理后有26个,用T0070907处理后有29个。此外,我们还检测到未处理的中期和后期黄体之间的基因表达差异(409个差异表达基因)。本研究揭示了一些新的候选基因,这些基因可能通过调节与卵巢类固醇生成、代谢过程、细胞分化、凋亡和免疫反应相关的信号通路,在控制黄体功能中发挥作用。这些发现为进一步研究解释PPARγ在生殖系统中的作用机制奠定了基础。