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Reproduction (Cambridge, England)2003; 125(6); 855-863; doi: 10.1530/rep.0.1250855

Production of capsular material by equine trophoblast transplanted into immunodeficient mice.

Abstract: A novel xenogeneic transplantation approach was used to determine whether it is embryonic or maternal tissue that produces the material that gives rise to the mucin-like glycoprotein of the equine embryonic capsule. Endometrial biopsy samples and conceptuses from six mares at days 13-15 after ovulation were prepared as 1 mm(3) grafts of endometrium, trophoblast and capsule for transplantation, alone or in combination, into various sites in 88 immunodeficient (severe combined immunodeficient or RAG2/gamma(c) double mutant) mice. The overall recovery rate of grafts was over 50%, reaching 100% with experience and use of the renal subcapsular space exclusively. Periodic acid-Schiff (PAS) staining demonstrated capsule-like extracellular glycoprotein secretions at the graft site in 11 of 22 sites examined. Strong PAS-positive reactions (5-7 microm thick) were found in four of six sites containing trophoblast alone, five of six endometrium plus trophoblast sites, and zero of eight grafts of endometrium alone. Two recovered grafts of capsule were also PAS-positive. The secreted glycoprotein was identified as equine embryonic capsule material by using a monoclonal antibody (mAb) specific to equine capsule (mAb OC-1) in two experiments. In the first, in cryosections, this antibody bound to 19 of 19 recovered trophoblast graft secretions (including those in 12 from mice that had not received endometrium at any site), ten of ten recovered endometrium plus trophoblast grafts, and zero of 12 recovered endometrial grafts from mice in which trophoblast had been grafted to the same site or another site in the same mouse. In the second experiment, in paraformaldehyde-fixed sections of grafts from 11 mice, specific staining, identical to that shown by grafted capsule, was obtained with grafts of trophoblast (both alone and in combination with endometrium) but not with grafts of endometrium. These results support the contention that trophoblast is the principal source of equine embryonic capsule. In addition, they demonstrate that xenogeneic grafting is a useful means of culturing endometrium and conceptus tissues outside the mare when in vitro techniques do not suffice.
Publication Date: 2003-05-30 PubMed ID: 12773108DOI: 10.1530/rep.0.1250855Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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This study investigates the origin of the material responsible for producing the mucin-like glycoprotein in the equine embryonic capsule. Using a new transplantation method on immunodeficient mice, the researchers have determined that the trophoblast tissue in equine embryos is the main source of this glycoprotein, proving invaluable for in vitro tissue cultures when other techniques are insufficient.

Methodology

  • The research made use of a unique xenogeneic transplantation approach to discern whether the embryonic or maternal tissue is responsible for the production of the equine embryonic capsule.
  • Endometrial biopsy samples and conceptuses from six mares were grafted into immunodeficient mice using primarily the renal subcapsular space. This procedure had a high recovery rate, going up to 100% with experience and consistent use of the renal subcapsular space.

Findings

  • Periodic Acid-Schiff (PAS) staining was applied to detect the presence of extracellular glycoprotein secretions that were capsule-like at the graft site. The staining was substantially present in the graft sites that contained the trophoblast alone or the trophoblast with the endometrium, but none were found within grafts of endometrium alone.
  • The secreted glycoprotein was identified as equine embryonic capsule material via a monoclonal antibody (mAb). Positive reactions were found in all recovered trophoblast graft secretions and grafts containing both endometrium and trophoblast. However, no positive reaction was found in the grafts of the endometrium alone.

Conclusion

  • The results from the antibody reactions and the PAS staining aligned to indicate that the trophoblast is the primary source of the equine embryonic capsule rather than the endometrium. This is a critical finding, as it confirms the origin of the mucin-like glycoprotein that constitutes the equine embryonic capsule.
  • Beyond confirming the source of the glycoprotein, the researchers also observed that xenogeneic grafting serves as a useful method for culturing endometrium and conceptus tissues outside the mare, particularly when in vitro techniques are not effective.

Cite This Article

APA
Albihn A, Waelchli RO, Samper J, Oriol JG, Croy BA, Betteridge KJ. (2003). Production of capsular material by equine trophoblast transplanted into immunodeficient mice. Reproduction, 125(6), 855-863. https://doi.org/10.1530/rep.0.1250855

Publication

ISSN: 1470-1626
NlmUniqueID: 100966036
Country: England
Language: English
Volume: 125
Issue: 6
Pages: 855-863

Researcher Affiliations

Albihn, A
  • Department of Biomedical Sciences, Ontario Veterinary College, Canada.
Waelchli, R O
    Samper, J
      Oriol, J G
        Croy, B A
          Betteridge, K J

            MeSH Terms

            • Animals
            • Antibodies, Monoclonal / pharmacology
            • Biopsy / methods
            • Embryo, Mammalian / immunology
            • Endometrium / metabolism
            • Endometrium / transplantation
            • Female
            • Horses
            • Immunohistochemistry / methods
            • Mice
            • Mice, SCID
            • Models, Animal
            • Transplantation, Heterologous
            • Trophoblasts / physiology
            • Trophoblasts / transplantation

            Citations

            This article has been cited 5 times.
            1. Swegen A. Maternal recognition of pregnancy in the mare: does it exist and why do we care?. Reproduction 2021 May 5;161(6):R139-R155.
              doi: 10.1530/REP-20-0437pubmed: 33957605google scholar: lookup
            2. Flesken-Nikitin A, Harlan BA, Nikitin AY. Transplantation Into the Mouse Ovarian Fat Pad. J Vis Exp 2016 Sep 7;(115).
              doi: 10.3791/54444pubmed: 27684746google scholar: lookup
            3. Park TS, Gavina M, Chen CW, Sun B, Teng PN, Huard J, Deasy BM, Zimmerlin L, Péault B. Placental perivascular cells for human muscle regeneration. Stem Cells Dev 2011 Mar;20(3):451-63.
              doi: 10.1089/scd.2010.0354pubmed: 20923371google scholar: lookup
            4. Jeschke U, Walzel H, Mylonas I, Papadopoulos P, Shabani N, Kuhn C, Schulze S, Friese K, Karsten U, Anz D, Kupka MS. The human endometrium expresses the glycoprotein mucin-1 and shows positive correlation for Thomsen-Friedenreich epitope expression and galectin-1 binding. J Histochem Cytochem 2009 Sep;57(9):871-81.
              doi: 10.1369/jhc.2009.952085pubmed: 19506091google scholar: lookup
            5. Bazer FW, Johnson GA. Early Embryonic Development in Agriculturally Important Species. Animals (Basel) 2024 Jun 26;14(13).
              doi: 10.3390/ani14131882pubmed: 38997994google scholar: lookup