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Placenta2001; 22(8-9); 749-767; doi: 10.1053/plac.2001.0707

A structural and immunological study of chorionic gonadotrophin production by equine trophoblast girdle and cup cells.

Abstract: Equine chorionic gonadotropin (eCG) production by the fetally derived endometrial cups appears to be necessary for the establishment and maintenance of normal equine pregnancy. Starting at about the 27th day of pregnancy, an equatorial band of trophectodermal cells on the surface of the spherical conceptus forms the chorionic girdle. This girdle consists initially of flat trophectodermal epithelium which corrugates into folds as the cells proliferate. The folds are then pressed against the uterine epithelium by expansion of the conceptus. The cells on the apices of the folds become binucleate before they start to invade the endometrium at days 35-37. Ultrastructural immunogold labelling shows that they begin to synthesize eCG as early as day 32, before they migrate into and through the maternal epithelium. Clusters of the girdle binucleate cells penetrate deep into the endometrium. The mature cup cell has a cytoplasm full of mitochondria, rough endoplasmic reticulum cisternae, a large Golgi apparatus and a strong immunoreactivity for the glucose transporter 1 isoform on its plasmalemma. Immunocytochemistry also demonstrates that eCG is localized in the Golgi cisternae, and in small dense granules similar to those found in the migrating girdle cell and present both in the Golgi region and at the peripheral plasmalemma. Release of eCG would therefore seem to be by the usual exocytotic mechanism as found for other protein hormones. The small size and absence of any significant accumulation of eCG-containing granules are in marked contrast to the numerous large luteinizing hormone (eLH) containing granules in the equine pituitary gonadotroph, although both hormones, eLH and eCG, show complete identity at the amino acid sequence level. These morphological indicators suggest that the cup cell secretes eCG constitutively (that is, continuously), with no requirement for secretagogues, whereas in the pituitary cell the regulated pathway is utilized capable of massive secretion under appropriate stimulation.
Publication Date: 2001-10-13 PubMed ID: 11597196DOI: 10.1053/plac.2001.0707Google Scholar: Lookup
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  • Journal Article

Summary

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This research article examines how embryonic horses produce a hormone called equine chorionic gonadotropin (eCG) during pregnancy. The researchers analyzed the structural and biological processes behind its formation and secretion.

Process of eCG Production

  • The research shows that eCG production starts around the 27th day of horse pregnancy, from an equatorial band of cells called the trophectodermal cells found on the surface of the conception sphere. This band forms the chorionic girdle.
  • The girdle initially consists of a flat trophectodermal epithelium that corrugates into folds as the cell proliferation progresses.
  • These folds are then pressed against the uterine epithelium as the conceptus grows. Some cells become binucleate, having two nuclei, before they start to penetrate the endometrium around days 35-37 of the pregnancy.

Early eCG Synthesis and Migration

  • Immunogold labelling, a technique used to visualize the location of proteins or other molecules in cells or tissues, shows that these cells begin to synthesize eCG as early as day 32, before they invade the maternal epithelium.
  • Clusters of binucleate cells from the girdle penetrate deep into the endometrium where they mature further.

Appearance of Mature Cup Cells

  • The cytoplasm of mature cup cells, which are involved in eCG production, is filled with mitochondria, rough endoplasmic reticulum cisternae, and a large Golgi apparatus.
  • Using immunocytochemistry, or the use of antibodies to visualize proteins, the research identifies strong immunoreactivity for glucose transporter 1 isoform on its plasmalemma, or the plasma membrane.
  • The researchers also found that eCG is localized in the Golgi cisternae, and small dense granules, similar to those found in the migrating cells.

Release of eCG Hormone

  • The research suggests the release of eCG presumably happens via exocytosis, the usual mechanism for other protein hormones.
  • Markers suggest cup cells continuously secrete eCG with no requirement for secretagogues, in contrast to pituitary cells which utilize a regulated pathway capable of massive secretion under appropriate stimulation.
  • This constant secretion of eCG is necessary for the establishment and maintenance of a normal equine pregnancy.

Distinct Hormonal Characteristics

  • The study notes a marked contrast in the small size and absence of significant accumulation of eCG-containing granules compared to the larger granules containing a hormone called luteinizing hormone (eLH) in the equine pituitary gonadotroph.
  • Interestingly, despite this difference in granule accumulation and their distinct roles in the body, both hormones share complete identity at the amino acid sequence level.

Cite This Article

APA
Wooding FB, Morgan G, Fowden AL, Allen WR. (2001). A structural and immunological study of chorionic gonadotrophin production by equine trophoblast girdle and cup cells. Placenta, 22(8-9), 749-767. https://doi.org/10.1053/plac.2001.0707

Publication

ISSN: 0143-4004
NlmUniqueID: 8006349
Country: Netherlands
Language: English
Volume: 22
Issue: 8-9
Pages: 749-767

Researcher Affiliations

Wooding, F B
  • The Physiological Laboratory, University of Cambridge, Downing Street, Cambridge, UK.
Morgan, G
    Fowden, A L
      Allen, W R

        MeSH Terms

        • Acid Phosphatase
        • Animals
        • Cell Membrane / chemistry
        • Chorionic Gonadotropin / analysis
        • Chorionic Gonadotropin / biosynthesis
        • Cytoplasm / chemistry
        • DNA / analysis
        • Endometrium / cytology
        • Endoplasmic Reticulum, Rough / chemistry
        • Epithelium / metabolism
        • Female
        • Gestational Age
        • Golgi Apparatus / chemistry
        • Horses
        • Immunohistochemistry
        • Isoenzymes
        • Luteinizing Hormone / analysis
        • Metalloproteins / analysis
        • Microscopy, Electron
        • Pituitary Gland, Anterior / chemistry
        • Pregnancy
        • Tartrate-Resistant Acid Phosphatase
        • Trophoblasts / metabolism
        • Trophoblasts / ultrastructure

        Citations

        This article has been cited 10 times.
        1. Vegas AR, Podico G, Canisso IF, Bollwein H, Fröhlich T, Bauersachs S, Almiñana C. Dynamic regulation of the transcriptome and proteome of the equine embryo during maternal recognition of pregnancy.. FASEB Bioadv 2022 Dec;4(12):775-797.
          doi: 10.1096/fba.2022-00063pubmed: 36479207google scholar: lookup
        2. Wooding FBP. The ruminant placental trophoblast binucleate cell: an evolutionary breakthrough.. Biol Reprod 2022 Sep 12;107(3):705-716.
          doi: 10.1093/biolre/ioac107pubmed: 35594454google scholar: lookup
        3. Antczak DF, Allen WRT. Placentation in Equids.. Adv Anat Embryol Cell Biol 2021;234:91-128.
          doi: 10.1007/978-3-030-77360-1_6pubmed: 34694479google scholar: lookup
        4. Read JE, Cabrera-Sharp V, Offord V, Mirczuk SM, Allen SP, Fowkes RC, de Mestre AM. Dynamic changes in gene expression and signalling during trophoblast development in the horse.. Reproduction 2018 Oct 1;156(4):313–330.
          doi: 10.1530/REP-18-0270pubmed: 30306765google scholar: lookup
        5. Read JE, Cabrera-Sharp V, Offord V, Mirczuk SM, Allen SP, Fowkes RC, de Mestre AM. Dynamic changes in gene expression and signalling during trophoblast development in the horse.. Reproduction 2018 Oct 1;156(4):313-330.
          doi: 10.1530/REP-18-0270pubmed: 29991567google scholar: lookup
        6. Cohen L, Bousfield GR, Ben-Menahem D. The recombinant equine LHβ subunit combines divergent intracellular traits of human LHβ and CGβ subunits.. Theriogenology 2015 Jun;83(9):1469-76.
        7. 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
        8. Antczak DF, de Mestre AM, Wilsher S, Allen WR. The equine endometrial cup reaction: a fetomaternal signal of significance.. Annu Rev Anim Biosci 2013 Jan;1:419-42.
        9. 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
        10. 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