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The American journal of anatomy1991; 192(4); 366-381; doi: 10.1002/aja.1001920405

Trophoblast-uterine interactions during equine chorionic girdle cell maturation, migration, and transformation.

Abstract: The structure of the equine chorionic girdle between days 28 and 42 of gestation was examined. Of particular interest were differentiation of trophoblastic cells within the girdle, adhesion between girdle and endometrium, invasion and displacement of the uterine epithelium, and the nature of the endometrium when girdle cells migrate into it to form endometrial cup cells. The chorionic girdle, identified initially as a band of tall columnar cells, becomes a stratified columnar epithelium indented by clefts and pits. Adhesion to and penetration through the endometrial luminal epithelium are rapid and occur initially in very limited areas. Stromal invasion occurs as strands of contiguous trophoblast cells invade through the basal lamina. Only girdle cells that are adjacent to the basal lamina or have entered the endometrial stroma undergo hypertrophy and differentiate into cup cells. At the initiation of trophoblastic invasion, the luminal epithelium contains numerous, large, intraepithelial, granular lymphocytes; small lymphocytes then accumulate in the stroma, but by day 42 lymphocytes are largely confined to the periphery of the cup. Although adhesion of trophoblast to the endometrial surface is initiated by small groups of girdle cells on restricted areas of the endometrial folds, the area is then increased by new areas of adhesion and by expansion of the initial invasion. Areas of girdle cells that do not attach undergo necrosis, as do superficial portions of areas of invasion. Consequently the girdle cells that form cups may be a minority of the original population. It is suggested that the differentiation of girdle cells is closely programmed and that cells that do not reach the stroma become necrotic at the same time that endometrial cup cells are differentiating.
Publication Date: 1991-12-01 PubMed ID: 1781447DOI: 10.1002/aja.1001920405Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • P.H.S.

Summary

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The study observes and provides insights into the interaction between trophoblast cells (part of the placenta) and the uterus in horses during the process of chorionic girdle cell maturation, migration, and transformation from 28th to 42nd day of gestation.

Study Methodology

  • The researchers closely examined the structure of the equine chorionic girdle from days 28 through 42 of gestation.
  • Key observations included the differentiation of trophoblast cells in the girdle, the adhesive process between the girdle and endometrium, the invasive process and displacement of uterine epithelium, and the characteristics of the endometrium during girdle cells’ migration to form endometrial cup cells.

Observations

  • In its initial stages, the chorionic girdle was identified as a band of tall columnar cells, which later develops into a stratified columnar epithelium forming indentations (clefts and pits).
  • The adhesion of trophoblast cells to the endometrial luminal epithelium and penetration through it were rapid, occurring initially in very limited areas.
  • Further interaction led to stromal invasion, with strands of trophoblast cells infiltrating the basal lamina.
  • Hypertrophy and differentiation into cup cells only take place in girdle cells adjacent to the basal lamina or those that have permeated the endometrial stroma.
  • During the initiation of trophoblastic invasion, the luminal epithelium had numerous granular lymphocytes, however, by day 42, they were largely confined to the cup periphery.

Conclusions

  • The adhesion of trophoblast to the endometrial surface is initiated by small clusters of girdle cells, and it expands by creating new adhesion areas and by enlarging the initial invasion space.
  • Areas of girdle cells that fail to attach undergo necrosis, as do the superficial sections of the invasion area.
  • The researchers suggest that the differentiation of girdle cells is highly programmed and cells failing to reach the stroma become necrotic concurrently to when endometrial cup cells differentiate.
  • The study indicates that the girdle cells that form cups could be a minority of the original population, a potentially significant insight for understanding placental development in horses.

Cite This Article

APA
Enders AC, Liu IK. (1991). Trophoblast-uterine interactions during equine chorionic girdle cell maturation, migration, and transformation. Am J Anat, 192(4), 366-381. https://doi.org/10.1002/aja.1001920405

Publication

ISSN: 0002-9106
NlmUniqueID: 0376312
Country: United States
Language: English
Volume: 192
Issue: 4
Pages: 366-381

Researcher Affiliations

Enders, A C
  • Department of Cell Biology and Human Anatomy, School of Medicine, University of California, Davis 95616.
Liu, I K

    MeSH Terms

    • Animals
    • Cell Death
    • Cell Differentiation
    • Cell Movement
    • Endometrium / ultrastructure
    • Female
    • Horses / anatomy & histology
    • Lymphocytes / ultrastructure
    • Pregnancy
    • Trophoblasts / ultrastructure

    Grant Funding

    • HD10342 / NICHD NIH HHS

    Citations

    This article has been cited 9 times.
    1. Zimmermann W, Kammerer R. The immune-modulating pregnancy-specific glycoproteins evolve rapidly and their presence correlates with hemochorial placentation in primates.. BMC Genomics 2021 Feb 18;22(1):128.
      doi: 10.1186/s12864-021-07413-8pubmed: 33602137google scholar: lookup
    2. Haig D. Comment on the exchange between Boddy et al. and Wagner et al.: malignancy, placentation and litter size.. Evol Med Public Health 2020;2020(1):217-218.
      doi: 10.1093/emph/eoaa027pubmed: 33214903google scholar: lookup
    3. McGowen MR, Erez O, Romero R, Wildman DE. The evolution of embryo implantation.. Int J Dev Biol 2014;58(2-4):155-61.
      doi: 10.1387/ijdb.140020dwpubmed: 25023681google scholar: lookup
    4. Cabrera-Sharp V, Read JE, Richardson S, Kowalski AA, Antczak DF, Cartwright JE, Mukherjee A, de Mestre AM. SMAD1/5 signaling in the early equine placenta regulates trophoblast differentiation and chorionic gonadotropin secretion.. Endocrinology 2014 Aug;155(8):3054-64.
      doi: 10.1210/en.2013-2116pubmed: 24848867google scholar: lookup
    5. Brosnahan MM, Miller DC, Adams M, Antczak DF. IL-22 is expressed by the invasive trophoblast of the equine (Equus caballus) chorionic girdle.. J Immunol 2012 May 1;188(9):4181-7.
      doi: 10.4049/jimmunol.1103509pubmed: 22490443google scholar: lookup
    6. Noronha LE, Huggler KE, de Mestre AM, Miller DC, Antczak DF. Molecular evidence for natural killer-like cells in equine endometrial cups.. Placenta 2012 May;33(5):379-86.
    7. de Mestre AM, Miller D, Roberson MS, Liford J, Chizmar LC, McLaughlin KE, Antczak DF. Glial cells missing homologue 1 is induced in differentiating equine chorionic girdle trophoblast cells.. Biol Reprod 2009 Feb;80(2):227-34.
      doi: 10.1095/biolreprod.108.070920pubmed: 18971425google scholar: lookup
    8. Carter AM, Enders AC. Comparative aspects of trophoblast development and placentation.. Reprod Biol Endocrinol 2004 Jul 5;2:46.
      doi: 10.1186/1477-7827-2-46pubmed: 15236656google scholar: lookup
    9. Enders AC, Meadows S, Stewart F, Allen WR. Failure of endometrial cup development in the donkey-in-horse model of equine abortion.. J Anat 1996 Jun;188 ( Pt 3)(Pt 3):575-89.
      pubmed: 8763475