36 research outputs found

    Influence of potting geometry of inserts load-carrying capability in sandwich structure

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    The work was supported from European Regional Development Fund-Project „Research and Development of Intelligent Components of Advanced Technologies for the Pilsen Metropolitan Area (InteCom)” (No. CZ.02.1.01/0.0/0.0/17_048/0007267) and from project SGS-2019-009 of the Czech Ministry of Education, Youth and Sports

    Embryo-lethal and teratogenic effect of the new platinum compound DPR in pregnant mice.

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    Demonstration of enzymes in cells cultured on semipermeable membrane in a double chamber

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    Cytoarchitecture modifications of the human uterine endocervical mucosa in long-term three-dimensional organotypic culture

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    We assayed the effects of phenol red (pr), estrogen (Es), and progesterone (Pg) in three-dimensional organotypic cultures of human uterine endocervix. Small intact fragments deposited on sponges submerged in DMEM with 10% fetal bovine serum were cultured in three different conditions: with pr (DMEM(pr+)), without pr (DMEM(pr-)), and without pr but with the addition of physiological concentrations of Es and Pg [DMEM(pr-)(Es+Pg)]. Cell viability and cellular responses were assayed after 4, 10, and 21 days using immunohistochemistry for the expression and distribution of the following markers: mucins and mucopolysaccharides (PAS staining), pan-cytokeratins (AE1/AE3), CK19, p63, Ki-67, vimentin, estrogen receptor-alpha (ER-alpha), and progesterone receptor (PR). The fragments cultivated in DMEM(pr+) showed a cuboidal, poorly differentiated epithelial phenotype and signs of stroma degeneration. In DMEM(pr-), both tissue architecture and cellular heterogeneity were much better preserved: epithelial cells showed a more columnar shape, and stroma was very well conserved, maintaining cell density. The addition of Es and Pg further improved the histology and physiology of the fragments: in DMEM(pr-)(Es+Pg), epithelial cells retained a columnar shape, secreted mucins, and formed areas of squamous hyperplasia
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