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Placenta2017; 58; 115-121; doi: 10.1016/j.placenta.2017.08.075

A lectin histochemical study to detect variation in glycosylation at the feto-maternal interface in three interbreeding equine species.

Abstract: In this study, we compare glycosylation at the fetomaternal interface in 3 equine species: horse, donkey and zebra, all of which can interbreed to produce hybrids, to assess their glycan similarities and differences. Methods: Sections cut from 3 specimens of horse (Equus caballus) placenta (50, 200 and 280 days gestation), one donkey (Equus asinus) placenta (65 cm crown-rump length) and 5 specimens of zebra (Equus quagga) placentae (81-239 days gestation) were stained with a panel of 24 biotinylated lectins using an avidin-peroxidase revealing system. Results: There were only slight quantitative differences in the lectin histochemistry at the feto-maternal interface between all three specimens; zebra placentae expressed more α2,6-linked sialic acid, with α1,2fucosyl residues at the microvillous interface. However, zebra trophoblast showed histological differences from the other two species, with polarised cells, prominent supranuclear Golgi bodies, and fewer intracellular granules. Conclusions: Our findings appear to confirm the hypothesis that closely related, interbreeding species with epitheliochorial placentae express similar glycans at the feto-maternal interface, thereby supporting the existence of a placental glycocode. We also observed intraspecies evolutionary diversion to be associated with a different histological architecture and the absence of significant intracellular granules.
Publication Date: 2017-09-04 PubMed ID: 28962689DOI: 10.1016/j.placenta.2017.08.075Google Scholar: Lookup
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  • Journal Article

Summary

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The research paper discusses a study investigating variations in glycosylation, a cellular process that attaches glycans to proteins or lipids, at the fetomaternal interface in three interbreeding types of equines: horses, donkeys, and zebras.

Methods

  • The study involved histological analysis of placental sections taken from three horses, one donkey, and five zebras, all at different stages of gestation.
  • The researchers utilized a lectin histochemical approach to analyze glycosylation. Lectin histochemistry involves using lectins, proteins that bind to specific carbohydrates, to detect and visualize certain types of glycosylation.
  • The placental samples were stained with a panel of 24 biotinylated lectins, and revelations were made using an avidin-peroxidase system (a common method to detect biotin, a type of B-vitamin).

Results

  • The findings showed only slight quantitative differences in lectin histochemistry at the fetomaternal interface across all three species.
  • Zebra placentas had more of a particular type of glycan, the α2,6-linked sialic acid, and showed α1,2fucosyl residues at a specific part of the placenta, the microvillous interface.
  • Zebra trophoblast, a type of cell that plays a key role in pregnancy, was found to be histologically different from that in horses or donkeys, with specific cellular structures being more prominent and fewer intracellular granules.

Conclusions

  • The team’s observations seemed to confirm their initial hypothesis that closely related species with epitheliochorial placentae (a type of placenta structure found in equines and other species) express similar types of glycans at the fetomaternal interface. This supports the existence of a placental glycocode – a concept suggesting that particular patterns of glycosylation might carry coded information.
  • The study also notes that slight histological differences were found within a species (intraspecies evolutionary diversion), possibly associated with different placental architectural features and the absence of significant intracellular granules.

Cite This Article

APA
Jones CJP, Allen WRT, Wilsher S. (2017). A lectin histochemical study to detect variation in glycosylation at the feto-maternal interface in three interbreeding equine species. Placenta, 58, 115-121. https://doi.org/10.1016/j.placenta.2017.08.075

Publication

ISSN: 1532-3102
NlmUniqueID: 8006349
Country: Netherlands
Language: English
Volume: 58
Pages: 115-121
PII: S0143-4004(17)31098-6

Researcher Affiliations

Jones, Carolyn J P
  • Maternal and Fetal Health Research Centre, Division of Developmental Biology and Medicine, School of Medical Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Oxford Road, Manchester M13 9WL, UK. Electronic address: carolyn.jones@manchester.ac.uk.
Allen, W R Twink
  • The Paul Mellon Laboratory, 'Brunswick', 18 Woodditton Road, Newmarket, Suffolk CB8 9BJ, UK.
Wilsher, Sandra
  • The Paul Mellon Laboratory, 'Brunswick', 18 Woodditton Road, Newmarket, Suffolk CB8 9BJ, UK.

MeSH Terms

  • Animals
  • Equidae
  • Female
  • Glycosylation
  • Histocytochemistry
  • Horses
  • Lectins / metabolism
  • Placenta / metabolism
  • Pregnancy
  • Trophoblasts / metabolism
  • Uterus / metabolism

Citations

This article has been cited 3 times.
  1. Ziganshina MM, Dolgushina NV, Kulikova GV, Fayzullina NM, Yarotskaya EL, Khasbiullina NR, Abdurakhmanova NF, Asaturova AV, Shchegolev AI, Dovgan AA, Sukhikh GT. Epithelial apical glycosylation changes associated with thin endometrium in women with infertility - a pilot observational study. Reprod Biol Endocrinol 2021 May 15;19(1):73.
    doi: 10.1186/s12958-021-00750-zpubmed: 33992099google scholar: lookup
  2. Shilova NV, Galanina OE, Polyakova SM, Nokel AY, Pazynina GV, Golovchenko VV, Patova OA, Mikshina PV, Gorshkova TA, Bovin NV. Specificity of widely used lectins as probed with oligosaccharide and plant polysaccharide arrays. Histochem Cell Biol 2024 Dec;162(6):495-510.
    doi: 10.1007/s00418-024-02323-8pubmed: 39182197google scholar: lookup
  3. Navarrete Zamora MB, da Silva TS, da Silva MD, Almeida GHDR, da Silva-Júnior LN, Horvath-Pereira BO, Baracho Hill AT, Acuña F, Carreira ACO, Barreto RDSN, Sato AS, Miglino MA. Term alpaca placenta glycosylation profile and its correlation with pregnancy maintenance and fetal survival. Front Cell Dev Biol 2023;11:1193468.
    doi: 10.3389/fcell.2023.1193468pubmed: 37342231google scholar: lookup