4.6 Article

Ovarian inflammatory mRNA profiles of a dehydroepiandrosterone plus high-fat diet-induced polycystic ovary syndrome mouse model

期刊

REPRODUCTIVE BIOMEDICINE ONLINE
卷 44, 期 5, 页码 791-802

出版社

ELSEVIER SCI LTD
DOI: 10.1016/j.rbmo.2021.10.024

关键词

Gene expression; Inflammation; Polycystic ovary syndrome; RNA sequencing

资金

  1. Chongqing Natural Science Foundation [cstc2020jcyj-msxmX0294, cstc2018jxj1130065, jxyn2019-2-7]
  2. Science and Technology Project of Chongqing Yuzhong District [20200103]
  3. National Natural Science Foundation of China [82171624, 82104923]
  4. Scientific Research and Innovation Experiment Project of Chongqing Medical University [SRIEP202002, SRIEP202106]
  5. Chongqing Municipal Health Bureau Chinese Medicine Technology Project [ZY20182044]

向作者/读者索取更多资源

This study investigated the expression pattern of inflammatory mRNA profiles in the ovarian tissues of a DHEA plus HFD-induced PCOS mouse model. The differentially expressed genes were found to be associated with PCOS inflammation and could potentially serve as therapeutic options against the disease.
Research question: What is the expression pattern of inflammatory mRNA profiles of a dehydroepiandrosterone (DHEA) plus high-fat diet (HFD)-induced polycystic ovary syndrome (PCOS) mouse model? Design: RNA sequencing was performed to investigate the mRNA expression profiles in the ovarian tissues of a DHEA plus HFD-induced PCOS mouse model. Six samples were divided into two groups (control and PCOS), with three biological replicates in each group. This was followed by hierarchical clustering, gene ontology and Kyoto Encyclopedia of Genes and Genomes pathway analyses. The relative expression levels of nine inflammatory genes were validated via quantitative reverse-transcription polymerase chain reaction. Results: A total of 436 genes were differentially expressed between the control and PCOS mice. Out of these, 137 genes were up-regulated while 299 genes were down-regulated. Gene ontology analysis indicated that differentially expressed mRNA were associated with T cell-mediated cytotoxicity and homocysteine metabolic processes. Pathway analysis further showed that these abnormally expressed mRNA were associated with signalling pathways, such as NF-kB signalling, tyrosine metabolism and phenylalanine metabolism. All these pathways are involved in chronic inflammation and PCOS. Conclusion: The differentially expressed genes are potentially involved in the inflammation that is evident in PCOS, and so could serve as therapeutic options against the disease. Nevertheless, prospective studies are needed to test this hypothesis.

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