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Cytokine2020; 137; 155307; doi: 10.1016/j.cyto.2020.155307

Expression profile of proinflammatory mediators in the placenta of mares during physiological detachment and retention of fetal membranes.

Abstract: Physiological parturition is characterized by sterile, inflammatory-like processes. During parturition, the placenta expresses various proinflammatory mediators, such as chemokines and IL-17. Nevertheless, inflammatory processes present in the parturient mare are poorly characterized. The aim of this study was to investigate the expression of selected chemokines and IL-17 in the allantochorion and the endometrium of mares that retained fetal membranes (RFM) and expelled them physiologically. We hypothesized that the expression of these mediators may be altered in the placenta of mares with RFM and result in RFM occurrence. Differences in mRNA expression in the placenta of investigated groups of mares were detected for CCL2, CCL3, CCL4, CCL8, CXCL1, CXCL8, CXCL10, CX3CL1 and IL-17. There were no differences in mRNA expression of CCL5 and CXCL6. Gene ontology network analysis showed enrichment in genes related to leukocyte migration, cell chemotaxis and response to chemokine in tissues of RFM mares. Analysis of association network suggested denotations between CXCL6, CXCL8, CXCL1, CCL5, CCL4, CX3CL1 and CXCL10. Moreover, possible inhibition of CXCL10 by IL-17A and prostaglandin peroxide synthase 2 (PTGS2) by CXCL1 was detected. Our results suggest that, based on differences in chemokines and IL-17 expression, recruited subsets of leukocytes might differ between the analyzed groups of mares, which in turn may impair the separation of fetal membranes in the group of RFM mares. In addition, the results of the expression analysis suggest that macrophages might be one of the most abundant cells infiltrating the equine placenta during the expulsion of fetal membranes. Furthermore, we suspect that the synthesis of PTGS2 might be inhibited in mares with RFM.
Publication Date: 2020-10-01 PubMed ID: 33011402DOI: 10.1016/j.cyto.2020.155307Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This study investigate the expression levels of specific chemokines and IL-17 in the placentas of mares that have retained their fetal membranes (RFM) during parturition, versus those that have expelled them normally. Their findings suggest that differences in chemokine expression and the types of immune cells recruited may contribute to RFM occurrence.

Background and Aim

  • The researchers aim to better understand the inflammatory processes that occur during physiological parturition (the process of giving birth) in mares.
  • They focus on a condition known as Retention of Fetal Membranes (RFM), where the placenta fails to be expelled post-parturition. This condition is poorly understood in horses.
  • The team hypothesizes that differences in the expression of certain proinflammatory mediators may contribute to RFM.

Methodology

  • Expression levels of selected chemokines (proteins that guide the movement of cells) and interleukin 17 (IL-17, a type of immune signalling molecule) were evaluated in the parts of the equine placenta (allantochorion and the endometrium).
  • Comparison was made between mares that had RFM and those that expelled their membranes normally.

Findings

  • Differences in mRNA expression in the placenta were observed among the mare groups for genes encoding for several chemokines and IL-17.
  • No differences were observed in the expression of CCL5 and CXCL6 genes.
  • Analysis suggested links among the expression patterns of several chemokines (CXCL6, CXCL8, CXCL1, CCL5, CCL4, CX3CL1 and CXCL10).
  • Possible inhibition of the chemokine CXCL10 by IL-17A and the enzyme PTGS2 by CXCL1 was also observed.

Implications

  • The study suggests that differences in expression of these proinflammatory mediators could influence the types of leukocytes (white blood cells) recruited to the site of inflammation, potentially affecting membrane separation.
  • The abundance of macrophages (a type of immune cell) in the placenta of mares could be a significant factor during normal expulsion of the fetal membranes.
  • It is also hypothesized that the synthesis of PTGS2, an enzyme involved in producing molecules that stimulate inflammation and pain, might be inhibited in mares with RFM, which could contribute to the disease.

Cite This Article

APA
Jaworska J, Ropka-Molik K, Kowalczyk-Zięba I, Boruszewska D, Wocławek-Potocka I, Siemieniuch M. (2020). Expression profile of proinflammatory mediators in the placenta of mares during physiological detachment and retention of fetal membranes. Cytokine, 137, 155307. https://doi.org/10.1016/j.cyto.2020.155307

Publication

ISSN: 1096-0023
NlmUniqueID: 9005353
Country: England
Language: English
Volume: 137
Pages: 155307
PII: S1043-4666(20)30323-9

Researcher Affiliations

Jaworska, Joanna
  • Department of Gamete and Embryo Biology, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, 10-747 Olsztyn, Poland. Electronic address: joanna.jaworska11@gmail.com.
Ropka-Molik, Katarzyna
  • Department of Animal Molecular Biology, National Research Institute of Animal Production, 32-083 Balice, Poland.
Kowalczyk-Zięba, Ilona
  • Department of Gamete and Embryo Biology, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, 10-747 Olsztyn, Poland.
Boruszewska, Dorota
  • Department of Gamete and Embryo Biology, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, 10-747 Olsztyn, Poland.
Wocławek-Potocka, Izabela
  • Department of Gamete and Embryo Biology, Institute of Animal Reproduction and Food Research, Polish Academy of Sciences, 10-747 Olsztyn, Poland.
Siemieniuch, Marta
  • Research Station of the Institute of Reproduction and Food Research, Polish Academy of Sciences in Popielno, 12-220 Ruciane-Nida, Poland.

MeSH Terms

  • Allantois / metabolism
  • Animals
  • Chemokines / genetics
  • Chemokines / metabolism
  • Chorion / metabolism
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Endometrium / metabolism
  • Extraembryonic Membranes / metabolism
  • Female
  • Gene Expression Profiling / methods
  • Horses
  • Inflammation Mediators / metabolism
  • Interleukin-17 / genetics
  • Interleukin-17 / metabolism
  • Placenta / metabolism
  • Pregnancy

Citations

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