Structural Differentiation of Human Uterine Luminal and Glandular Epithelium during Early Pregnancy: An Ultrastructural and Immunohistochemical Study

The differentiation of human endometrial epithelium is a dynamic event that occurs throughout the menstrual cycle and early pregnancy. The structural transformation and differentiation of human uterine luminal and glandular epithelium of early human pregnancy (n=14) was investigated ultrastructurall...

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Veröffentlicht in:Placenta (Eastbourne) 2002-09, Vol.23 (8-9), p.672-684
Hauptverfasser: Demir, R., Kayisli, U.A., Celik-Ozenci, C., Korgun, E.T., Demir-Weusten, A.Y., Arici, A.
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container_issue 8-9
container_start_page 672
container_title Placenta (Eastbourne)
container_volume 23
creator Demir, R.
Kayisli, U.A.
Celik-Ozenci, C.
Korgun, E.T.
Demir-Weusten, A.Y.
Arici, A.
description The differentiation of human endometrial epithelium is a dynamic event that occurs throughout the menstrual cycle and early pregnancy. The structural transformation and differentiation of human uterine luminal and glandular epithelium of early human pregnancy (n=14) was investigated ultrastructurally and immunohistochemically using antibodies against cytokeratin (CT), endothelial marker CD31, Fas, and proliferating cell nuclear antigen (PCNA). Ultrastructurally, luminal epithelial cells showed distinctive euchromatic nuclei with prominent nucleoli and relatively loose cell membranes in all poles (apical to basal). Subcellular components were easily recognized in luminal epithelium except in degenerating cells. Mainly two cell types, dark and clear cells, formed the glandular epithelium. In the early gestation period, microvilli were abundant on the apical and apico-lateral poles of these cells. Only a few cytoplasmic projections were observed in dark cells. Numerous cilia were observed on the apical pole of some clear cells, located at the adluminal segment. In contrast, dark cells lacked cilia, nuclear channels, or giant mitochondrial profiles. Glycogen synthesis and apocrine secretion were recognizable for several days during early gestation. The apocrine secretory activity differed among dark cells of the glandular epithelium. The immunoreactivity of PCNA and Fas, and ultrastructural observations in the glandular epithelium suggest that, even in different segments of the same gland, epithelial cells do not regress during early gestation, but proliferate, perhaps representing a resistance against trophoblastic invasion. These morphological and molecular changes suggest that both luminal and glandular epithelium may play an important role in cellular defense and limitation for trophoblastic invasion during early pregnancy since plasma membrane alterations of the surface epithelium take place at the apical, basal and lateral poles compared to early secretory phase endometrial cells. Besides glandular epithelium may be consequently responsible for uterine secretions, which may be critical for early embryo development.
doi_str_mv 10.1053/plac.2002.0841
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Besides glandular epithelium may be consequently responsible for uterine secretions, which may be critical for early embryo development.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>12361686</pmid><doi>10.1053/plac.2002.0841</doi><tpages>13</tpages></addata></record>
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subjects Adult
Apoptosis - physiology
Biological and medical sciences
Biomarkers
Cell Differentiation
Cell Division - physiology
Decidua - cytology
Decidua - metabolism
Embryo Implantation - physiology
Epithelium - metabolism
Epithelium - ultrastructure
fas Receptor - metabolism
Female
Fluorescent Antibody Technique, Indirect
Fundamental and applied biological sciences. Psychology
Gestational Age
Humans
Immunoenzyme Techniques
Keratins - metabolism
Microscopy, Electron
Microvilli - ultrastructure
Mother. Fetoplacental unit. Mammary gland. Milk
Pregnancy
Pregnancy. Parturition. Lactation
Proliferating Cell Nuclear Antigen - metabolism
Vertebrates: reproduction
title Structural Differentiation of Human Uterine Luminal and Glandular Epithelium during Early Pregnancy: An Ultrastructural and Immunohistochemical Study
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