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Molecules of the early equine trophoblast.

Abstract: Three monoclonal antibodies raised against equine trophoblast cells were tested to determine the characteristics of the identified molecules. First, the antibodies were used to precipitate molecules from radiolabelled equine trophoblast cells of the chorionic girdle. Antibody F71.1 precipitated a molecule of 115 kDa, whereas antibodies 71.8 and 71.10 precipitated a molecule of 66 kDa. Second, 2 of the antibodies were used in an indirect immunoperoxidase assay on frozen sections of equine conceptuses of different gestational ages beginning at Day 8. Antibody F71.1 labelled trophoblast cells from Day 13 onward, whereas antibody F71.8 first labelled trophoblast cells beginning on Day 24. Third, the antibodies were tested for reactivity with first trimester human placental tissues using an indirect immunoperoxidase assay. Antibody F71.1 labelled villous cytotrophoblast cells, whereas antibody F71.8 labelled only the syncytiotrophoblast cells. Neither antibody reacted with extra-villous trophoblast cells. The molecular weight and tissue distribution of the antigen identified by antibody F71.8 suggest that it may be a placental form of alkaline phosphatase. The molecule identified by antibody F71.1 was first detected very close to the time of maternal recognition of pregnancy in the mare.
Publication Date: 1991-01-01 PubMed ID: 1795290
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • Non-P.H.S.
  • Research Support
  • U.S. Gov't
  • P.H.S.

Summary

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This research paper investigates the characteristics and roles of various molecules in horse trophoblast cells using three different monoclonal antibodies. The study further compares the reactivity of these antibodies with human placental tissues, providing deeper insights into the similarity between horse and human reproductive techniques.

Conducting Experiments With Monoclonal Antibodies

  • The experiment started with the use of three monoclonal antibodies raised against equine trophoblast cells. They aimed to identify the molecules’ characteristics these antibodies would recognize.
  • Antibody F71.1 precipitated a molecule of 115 kDa, whereas antibodies 71.8 and 71.10 precipitated a molecule of 66 kDa. These molecules were extracted from radiolabelled equine trophoblast cells of the chorionic girdle—a specialized part of equine placenta—using the antibodies.
  • The antibodies’ reactivity was tested at different gestational age periods. This examination showed that antibody F71.1 labelled trophoblast cells from Day 13 onward while antibody F71.8 started labelling cells from Day 24.

Testing on Human Placental Tissues

  • After analyzing the effects of antibodies on equine trophoblast cells, the researchers proceeded to test the antibodies’ reactivity with human placental tissues.
  • Through the use of an indirect immunoperoxidase assay—an investigative method that determines antibody-antigen interactions—a distinction was made in the effect of the two antibodies upon different cell types. Antibody F71.1 labelled villous cytotrophoblast cells, whereas antibody F71.8 labelled only the syncytiotrophoblast cells.
  • However, neither antibody reacted with extra-villous trophoblast cells—cells that anchor the placenta to the womb’s wall.

Conclusions and Implications

  • The experiment showed that the molecular weight and distribution of the antigen recognized by antibody F71.8 could be a placental form of alkaline phosphatase—a key enzyme in pregnant mammals. However, this conclusion would require further validation.
  • Interestingly, the molecule identified by antibody F71.1 was first detected very close to the time of maternal recognition of pregnancy in the mare, hinting at its possible importance in the early stages of equine pregnancy.
  • The findings also reinforce the idea of commonality in some aspects of the reproductive mechanisms of equines and humans despite the species’ differences.

Cite This Article

APA
Oriol JG, Donaldson WL, Dougherty DA, Antczak DF. (1991). Molecules of the early equine trophoblast. J Reprod Fertil Suppl, 44, 455-462.

Publication

ISSN: 0449-3087
NlmUniqueID: 0225652
Country: England
Language: English
Volume: 44
Pages: 455-462

Researcher Affiliations

Oriol, J G
  • James A. Baker Institute for Animal Health, New York State College of Veterinary Medicine, Cornell University, Ithaca 14853.
Donaldson, W L
    Dougherty, D A
      Antczak, D F

        MeSH Terms

        • Animals
        • Antibodies, Monoclonal
        • Cross Reactions / immunology
        • Female
        • Horses / embryology
        • Horses / immunology
        • Molecular Weight
        • Precipitin Tests
        • Pregnancy
        • Pregnancy, Animal / immunology
        • Pregnancy, Animal / metabolism
        • Trophoblasts / chemistry
        • Trophoblasts / immunology

        Citations

        This article has been cited 2 times.
        1. Tachibana Y, Sakurai T, Bai H, Shiota K, Nambo Y, Nagaoka K, Imakawa K. RNA-seq analysis of equine conceptus transcripts during embryo fixation and capsule disappearance.. PLoS One 2014;9(12):e114414.
          doi: 10.1371/journal.pone.0114414pubmed: 25514169google scholar: lookup
        2. de Mestre AM, Hanlon D, Adams AP, Runcan E, Leadbeater JC, Erb HN, Costa CC, Miller D, Allen WR, Antczak DF. Functions of ectopically transplanted invasive horse trophoblast.. Reproduction 2011 Jun;141(6):849-56.
          doi: 10.1530/REP-10-0462pubmed: 21389079google scholar: lookup