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Theriogenology2008; 71(2); 264-274; doi: 10.1016/j.theriogenology.2008.07.008

Immunohistochemical and histochemical identification of proteins and carbohydrates in the equine endometrium Expression patterns for mares suffering from endometrosis.

Abstract: Although alterations in patterns of protein secretion revealed in uterine flushings from mares suffering from endometrosis have been described, little is known about alterations at the cellular level. Hence, the aim of this study was to characterize deviations in patterns of uterine gland secretion patterns using endometrial biopsies, histochemical and newly established immunohistochemical methods. Forty-eight endometrial biopsies were obtained from mares suffering from various types of endometrosis (active and inactive, destructive and non-destructive) and degree (mild to severe) were analyzed for expression of the proteins uteroglobin, uteroferrin, calbindinD9k and uterocalin as representatives of endometrial proteins detectable by immunohistochemistry using polyclonal antibodies. Glycogen was identified using the PAS-reaction and mucopolysaccharides were stained with alcian blue. Uterine glandular epithelia within fibrotic foci mostly revealed a protein and carbohydrate pattern of expression which was independent of hormonal changes during the estrous cycle. In comparison to non-affected glands, most epithelial cells within periglandular fibrosis exhibited decreased immunostaining intensity for proteins, especially when there was destructive endometrosis. However, uteroferrin staining intensity was strong within areas of severe destructive endometrosis. Moreover, only few basal glandular epithelial cells, especially those in cystic glands, stained for mucopolysaccharides that are typically seen within the luminal epithelia. Usually a single fibrotic focus caused only slight alterations in glandular proteins and carbohydrate reaction patterns, so that only more severe endometrosis lead to deviations which were detectable in uterine flushings. The highly sensitive methods used in the present study allow studies of uterine secretion patterns in the context of routine assessment of endometrial biopsies.
Publication Date: 2008-08-31 PubMed ID: 18762329DOI: 10.1016/j.theriogenology.2008.07.008Google Scholar: Lookup
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  • Journal Article

Summary

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The research paper studies the deviations in the secretion patterns of the uterine gland in mares affected by endometrosis using endometrial biopsies, histochemical and newly established immunohistochemical methods. It reveals that fibrotic foci in uterine glandular epithelia have a distinct protein and carbohydrate pattern of expression which is not influenced by hormonal changes during the estrous cycle.

Research Objectives and Methods

  • The aim of the study was to determine variations in the secretion patterns of the uterine gland at the cellular level in mares suffering from endometrosis. Different types and degrees (mild to severe, active and inactive, destructive and non-destructive) of endometrosis were studied.
  • The researchers obtained forty-eight endometrial biopsies from affected mares. The expression of certain proteins (uteroglobin, uteroferrin, calbindinD9k, and uterocalin) that can be identified by immunohistochemistry using polyclonal antibodies were examined.
  • A histochemical method, the PAS-reaction, was used to identify glycogen and mucopolysaccharides were stained with alcian blue.

Key Findings

  • The uterine glandular epithelia within fibrotic foci exhibited a pattern of protein and carbohydrate expression largely independent of hormonal changes during the estrous cycle.
  • Compared to non-affected glands, the study found that most epithelial cells in areas affected by periglandular fibrosis exhibited a decreased intensity of immunostaining for proteins, especially in the case of destructive endometrosis.
  • However, cervical mucus staining intensity was strong within the areas of severe destructive endometrosis.
  • Only a few basal glandular epithelial cells, specifically within cystic glands, stained for mucopolysaccharides. This behavior is typically seen within the luminal epithelia.
  • The study also found that slight alterations in glandular proteins and carbohydrate reaction patterns caused by only a single fibrotic focus were generally identified in uterine flushings. These were more detectable in cases of severe endometrosis.
  • The high sensitivity of the methods used in this study facilitates further studies on uterine secretion patterns in the context of routine evaluations of endometrial biopsies.

Cite This Article

APA
Hoffmann C, Bazer FW, Klug J, Aupperle H, Ellenberger C, Schoon HA. (2008). Immunohistochemical and histochemical identification of proteins and carbohydrates in the equine endometrium Expression patterns for mares suffering from endometrosis. Theriogenology, 71(2), 264-274. https://doi.org/10.1016/j.theriogenology.2008.07.008

Publication

ISSN: 0093-691X
NlmUniqueID: 0421510
Country: United States
Language: English
Volume: 71
Issue: 2
Pages: 264-274

Researcher Affiliations

Hoffmann, C
  • Institute of Veterinary Pathology of the Faculty of Veterinary Medicine, University of Leipzig, An den Tierkliniken 33, 04103 Leipzig, Germany. christine.hoffmann@fli.bund.de
Bazer, F W
    Klug, J
      Aupperle, H
        Ellenberger, C
          Schoon, H-A

            MeSH Terms

            • Acid Phosphatase / metabolism
            • Animals
            • Calbindins
            • Carbohydrate Metabolism
            • Endometriosis / metabolism
            • Endometriosis / veterinary
            • Endometrium / metabolism
            • Female
            • Gene Expression Profiling / veterinary
            • Gene Expression Regulation / physiology
            • Glycogen / metabolism
            • Glycosaminoglycans / metabolism
            • Horse Diseases / metabolism
            • Horses
            • Immunohistochemistry / veterinary
            • Isoenzymes / metabolism
            • Lipocalins / genetics
            • Lipocalins / metabolism
            • Proteins / metabolism
            • S100 Calcium Binding Protein G / genetics
            • S100 Calcium Binding Protein G / metabolism
            • Tartrate-Resistant Acid Phosphatase
            • Uteroglobin / genetics
            • Uteroglobin / metabolism

            Citations

            This article has been cited 10 times.
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