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Molecular reproduction and development2012; 79(11); 777-784; doi: 10.1002/mrd.22112

Gene profiling of inflammatory genes in day 18 endometria from pregnant and non-pregnant mares.

Abstract: Maternal recognition of pregnancy is a physiological process that primarily describes endometrial responses to a conceptus. Recognition of a conceptus prevents the release of prostaglandin F(2α) , thereby ensuring survival of the corpus luteum and continued progesterone production. Exactly how this occurs in the mare is poorly understood. Because prostaglandin F(2α) is a pro-inflammatory hormone, we hypothesized that differential gene expression in the endometrium at the time of maternal recognition reflects an anti-inflammatory event leading to decreased prostaglandin F(2α) secretion. Mares were inseminated, and endometrial biopsies were recovered from pregnant mares on Day 18 post-ovulation. In subsequent estrous cycles, mares were not inseminated and Day 18 post-ovulation endometrial biopsies were collected (non-pregnant control, matched per individual). Endometrial gene expression profiles were examined by screening an Affymetrix equine GeneChip containing probes specific for genes related to inflammatory processes. Microarray analysis revealed 118 genes that were up-regulated and 93 genes that were down-regulated (P < 0.001) at least 1.5-fold in the endometrium of pregnant versus non-pregnant mares. Quantitative, real-time RT-PCR confirmed the microarray results for three up-regulated genes homologous to TSC22D3, PPAPDC2, and KLF6, and three down-regulated genes homologous to ESR1, MARCKSL1, and EPSTI1 (P < 0.05). It is concluded that the presence of the equine embryo induces differential gene expression in the endometrium of Day 18 pregnant mares, and that these genes are associated with inflammatory processes and pathways involving cellular growth and proliferation. The results from this study provide important new insights into endometrial gene expression in response to early equine pregnancy.
Publication Date: 2012-09-28 PubMed ID: 22968947DOI: 10.1002/mrd.22112Google Scholar: Lookup
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  • Journal Article

Summary

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This study investigates the processes within a horse’s uterine lining (endometrium) around day 18 of pregnancy to better understand how the body recognizes and supports the early stages of pregnancy. The research shows that early equine pregnancy impacts the gene expression within the endometrium, particularly those genes involved with inflammation and cell growth.

Research Methodology

  • The researchers’ methodology involved inseminating mares and obtaining endometrial biopsies from pregnant mares on Day 18 post-ovulation.
  • For control purposes, during subsequent estrous cycles, mares were not inseminated and Day 18 post-ovulation endometrial biopsies were also taken.
  • They used an Affymetrix equine GeneChip (microarray technology) to track gene expression profiles. This chip was specially designed with probes that screen for genes linked to inflammation processes.

Major Findings

  • Analysis showed that 118 genes were more active (up-regulated), while 93 genes were less active (down-regulated) in the endometrium of pregnant mares when compared to non-pregnant mares.
  • The changes were significant, with at least a 1.5-fold difference in activity.
  • The team confirmed these results using quantitative, real-time RT-PCR for a few select genes.
  • Increased expression was seen for genes TSC22D3, PPAPDC2, and KLF6 that have homologous function in humans, while the expression of genes ESR1, MARCKSL1, and EPSTI1 with homologous function in humans was decreased.

Conclusions

  • The different gene expression observed around Day 18 in pregnant mares, the researchers concluded, likely reflects an anti-inflammatory reaction that reduces the production of a particular hormone (prostaglandin F(2α)) that could cause the termination of pregnancy by letting the corpus luteum (a temporary structure that is crucial in maintaining pregnancy) die off.
  • This implies that the presence of an embryo in the equine uterus triggers gene activity adjustments within the endometrium.
  • The genes with changed expression are related to inflammation processes and pathways involving cellular growth and proliferation, suggesting their potential role in maternal recognition or support of early pregnancy.
  • These findings provide important insights into the body’s genetic responses during the early stages of equine pregnancy and may contribute to the understanding of pregnancy in other species, possibly including humans.

Cite This Article

APA
Patterson AL, Squires EL, Hansen TR, Bouma GJ, Bruemmer JE. (2012). Gene profiling of inflammatory genes in day 18 endometria from pregnant and non-pregnant mares. Mol Reprod Dev, 79(11), 777-784. https://doi.org/10.1002/mrd.22112

Publication

ISSN: 1098-2795
NlmUniqueID: 8903333
Country: United States
Language: English
Volume: 79
Issue: 11
Pages: 777-784

Researcher Affiliations

Patterson, Amanda L
  • Department of Animal Science, Colorado State University, Fort Collins, Colorado 80523-1680, USA.
Squires, Edward L
    Hansen, Thomas R
      Bouma, Gerrit J
        Bruemmer, Jason E

          MeSH Terms

          • Animals
          • Corpus Luteum / physiology
          • Dinoprost / biosynthesis
          • Dinoprost / metabolism
          • Down-Regulation
          • Endometrium / immunology
          • Endometrium / metabolism
          • Estrous Cycle / metabolism
          • Female
          • Gene Expression
          • Gene Expression Profiling
          • Horses
          • Inflammation / genetics
          • Inflammation / veterinary
          • Pregnancy
          • Pregnancy, Animal
          • Progesterone / metabolism
          • Up-Regulation

          Citations

          This article has been cited 1 times.
          1. Lekva T, Lyle R, Roland MC, Friis C, Bianchi DW, Jaffe IZ, Norwitz ER, Bollerslev J, Henriksen T, Ueland T. Gene expression in term placentas is regulated more by spinal or epidural anesthesia than by late-onset preeclampsia or gestational diabetes mellitus. Sci Rep 2016 Jul 11;6:29715.
            doi: 10.1038/srep29715pubmed: 27405415google scholar: lookup