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Animal reproduction science2022; 245; 107064; doi: 10.1016/j.anireprosci.2022.107064

Endometrial and luteal gene expression of putative gene regulators of the equine maternal recognition of pregnancy.

Abstract: Our understanding of the temporal changes in endometrial and luteal gene transcripts related to the actions of oxytocin and prostaglandin during early equine pregnancy is incomplete. Additionally, the role of oxytocinase, also known as Leucyl-cystinyl aminopeptidase (LNPEP), during early pregnancy in mares has not been previously investigated. Luteal and endometrial biopsies were obtained on Day (D)8, D10, D12 and D15 post-ovulation in pregnant (PREG) and diestrus (DIEST) mares for real-time qPCR. Differences in endometrial gene expression occurred over time in: SLC2A4, SLC2A1, PTGES, OXTR and LNPEP. PTGFR and PLA2G2C had lower relative abundance in PREG D15 endometrium compared to D10. OXT and OXTR were increased on D10 and 15 PREG, respectively. Regarding luteal mRNA relative abundance, ESR1, PTGS2, PTGFR, and PTGES had higher relative abundance in D12 of DIEST and PREG. Luteal expression of OXTR and OXT had higher relative abundance in D15 compared to D8, and LNPEP had higher relative abundance in D10 and 12. Endometrial and luteal PTGES had an increased mRNA abundance in both D12 DIEST and PREG mares, which may lead to additional luteoprotective prostaglandin E2 (PGE2) secretion. Furthermore, luteal SLC2A1 had higher relative abundance in pregnancy, and likely supports the high metabolic activity of luteal tissue by increasing glucose uptake. Oxytocinase is present in endometrial and luteal tissue and its role in oxytocin induced prostaglandin secretion is uncertain.
Publication Date: 2022-09-01 PubMed ID: 36087407DOI: 10.1016/j.anireprosci.2022.107064Google Scholar: Lookup
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  • Journal Article

Summary

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The research paper focuses on enhancing our understanding of changes in gene expression relating to oxytocin and prostaglandin activity during early stages of equine pregnancy. The study mainly investigated the role of oxytocinase in luteal and endometrial tissues at different post-ovulation days in pregnant and diestrus mares.

Methods and Findings

  • Biopsies were acquired from endometrial and luteal tissues in horses on days 8, 10, 12 and 15 after ovulation, both in pregnant and diestrus (non-pregnant) states. These samples were examined through real-time qPCR, a technique for determining gene expressions.
  • The research discovered time-dependent variations in endometrial gene expression for SLC2A4, SLC2A1, PTGES, OXTR, and LNPEP. The gene expression varied over time meaning it was not constant at different stages of the pregnancy.
  • Between day 10 and day 15 of pregnancy, a lower relative abundance was found in PTGFR and PLA2G2C genes in the endometrial tissue.
  • On the other hand, the OXT and OXTR genes were found to display higher expressions on days 10 and 15 of pregnancy, implying their critical roles at these stages.
  • In the luteal tissue, an increased relative abundance of ESR1, PTGS2, PTGFR, PTGES gene transcripts was discovered on day 12, both in pregnant and diestrus states.
  • Also, a sharp increase was noticed in the expression of OXTR and OXT genes, while LNPEP had higher relative abundance on days 10 and 12.

Implication of Findings

  • In the context of the study, relative abundance refers to the relative amount of a specific gene present at a given time. It gives an indication of the degree of gene expression.
  • The variations in gene expressions could influence prostaglandin secretion. Prostaglandin E2 (PGE2) has a vital role in pregnancy due to its protective influence on the luteal tissue.
  • Enhancement of SLC2A1 gene expression during pregnancy likely supports the high metabolic activity of luteal tissue by increasing glucose uptake.
  • One significant finding was the presence of oxytocinase (LNPEP) in both endometrial and luteal tissues. The role of this enzyme in oxytocin-induced prostaglandin secretion, however, remains unclear and might need further investigation.

Cite This Article

APA
Diel de Amorim M, Bramer SA, Rajamanickam GD, Klein C, Card C. (2022). Endometrial and luteal gene expression of putative gene regulators of the equine maternal recognition of pregnancy. Anim Reprod Sci, 245, 107064. https://doi.org/10.1016/j.anireprosci.2022.107064

Publication

ISSN: 1873-2232
NlmUniqueID: 7807205
Country: Netherlands
Language: English
Volume: 245
Pages: 107064
PII: S0378-4320(22)00143-9

Researcher Affiliations

Diel de Amorim, Mariana
  • Department of Clinical Sciences, Cornell University, 930 Campus Rd, Ithaca, NY 14853, USA. Electronic address: md649@cornell.edu.
Bramer, Sarah A
  • Department of Veterinary Clinical and Diagnostic Science, University of Calgary, 2500 University Drive NW, Calgary, Alberta T2N 1N4, Canada.
Rajamanickam, Gayathri D
  • Department of Veterinary Clinical and Diagnostic Science, University of Calgary, 2500 University Drive NW, Calgary, Alberta T2N 1N4, Canada.
Klein, Claudia
  • Department of Veterinary Clinical and Diagnostic Science, University of Calgary, 2500 University Drive NW, Calgary, Alberta T2N 1N4, Canada.
Card, Claire
  • Department of Large Animal Clinical Sciences, Western College of Veterinary Medicine, 52 Campus Drive, Saskatoon, SK S7N 5B4, Canada. Electronic address: claire.card@usask.ca.

MeSH Terms

  • Animals
  • Cyclooxygenase 2 / metabolism
  • Cystinyl Aminopeptidase / genetics
  • Cystinyl Aminopeptidase / metabolism
  • Dinoprostone / metabolism
  • Endometrium / metabolism
  • Female
  • Gene Expression
  • Glucose / metabolism
  • Horses / genetics
  • Oxytocin / pharmacology
  • Pregnancy
  • Prostaglandins / metabolism
  • RNA, Messenger / metabolism

Conflict of Interest Statement

Competing interests statement The authors declare no conflicts of interest.

Citations

This article has been cited 5 times.
  1. Ma Q, Chang L, Wang W, Che L, Song X, Li G, Zhang Y, Chen Y, Gu Z, Ge X. Leucyl and Cystinyl Aminopeptidase as a Prognostic-Related Biomarker in OV Correlating with Immune Infiltrates. Pharmgenomics Pers Med 2023;16:551-568.
    doi: 10.2147/PGPM.S400145pubmed: 37293607google scholar: lookup
  2. Newcombe JR, Cuervo-Arango J, Wilsher S. The Timing of the Maternal Recognition of Pregnancy Is Specific to Individual Mares. Animals (Basel) 2023 May 22;13(10).
    doi: 10.3390/ani13101718pubmed: 37238148google scholar: lookup
  3. Diel de Amorim M, Dong L, Byron M, Foster RA, Klein C, Saleh M, Saleh T, Card C. Characterization of serum and tissue oxytocinase and tissue oxytocin in the pregnant and non-pregnant mare. Sci Rep 2023 Mar 21;13(1):4616.
    doi: 10.1038/s41598-023-31540-9pubmed: 36944665google scholar: lookup
  4. Ramsaran LN, Byron M, Parry S, Lection J, Back B, Grenier J, Cheong SH, Diel de Amorim M. Investigation of gene stability in equine luteal tissue during mid-diestrus phase and early pregnancy - Research Article. BMC Vet Res 2026 Jan 9;22(1):84.
    doi: 10.1186/s12917-025-05241-6pubmed: 41507934google scholar: lookup
  5. Hidalgo I, Sorolla MA, Sorolla A, Salud A, Parisi E. Secreted Phospholipases A2: Drivers of Inflammation and Cancer. Int J Mol Sci 2024 Nov 19;25(22).
    doi: 10.3390/ijms252212408pubmed: 39596471google scholar: lookup