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10.1038/srep44616

http://scihub22266oqcxt.onion/10.1038/srep44616
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C5356009!5356009!28303918
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suck abstract from ncbi


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pmid28303918      Sci+Rep 2017 ; 7 (ä): ä
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  • Effects of matrix stiffness on epithelial to mesenchymal transition-like processes of endometrial epithelial cells: Implications for the pathogenesis of endometriosis #MMPMID28303918
  • Matsuzaki S; Darcha C; Pouly JL; Canis M
  • Sci Rep 2017[]; 7 (ä): ä PMID28303918show ga
  • Endometriosis is defined as the presence of endometrial glands and stroma within extrauterine sites. Our previous study revealed an epithelial to mesenchymal transition (EMT)-like process in red peritoneal endometriosis, whereas membrane localization of E-cadherin was well maintained in epithelial cells of deep infiltrating endometriosis (DIE). Here we show that endometrial epithelial cells (EEE) grown on polyacrylamide gel substrates (PGS) of 2 kilopascal (kPa), a soft matrix, initiate a partial EMT-like process with transforming growth factor-?1 (TGF-?1) stimulation. Increasing matrix stiffness with TGF-?1 stimulation reduced the number of cell-cell contacts. Cells that retained cell-cell contacts showed decreased expression of E-cadherin and zonula occludens 1 (ZO-1) to cell-cell junctions. Few deep endometriotic epithelial cells (DEE) grown on 30-kPa PGS, which may mimic in vivo tissue compliance of DIE, retained localization of E-cadherin to cell-cell junctions with TGF-?1 treatment. Immunohistochemical analysis showed no phosphorylated Smad 2/3 nuclear localization in E-cadherin+ epithelial cells of DIE. We hypothesize that EEE may undergo an EMT-like process after attachment of endometrium to peritoneum in a TGF-?1?rich microenvironment. However, TGF-?1 signaling may be absent in DIE, resulting in a more epithelial cell-like phenotype in a rigid microenvironment.
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