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10.1186/s12931-018-0841-9

http://scihub22266oqcxt.onion/10.1186/s12931-018-0841-9
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C6056940!6056940!30041633
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suck abstract from ncbi


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pmid30041633      Respir+Res 2018 ; 19 (ä): ä
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  • Human alveolar epithelial cells type II are capable of TGF?-dependent epithelial-mesenchymal-transition and collagen-synthesis #MMPMID30041633
  • Goldmann T; Zissel G; Watz H; Drömann D; Reck M; Kugler C; Rabe KF; Marwitz S
  • Respir Res 2018[]; 19 (ä): ä PMID30041633show ga
  • Background: The origin of collagen-producing cells in lung fibrosis is unclear. The involvement of embryonic signaling pathways has been acknowledged and trans-differentiation of epithelial cells is discussed critically. The work presented here investigates the role of TGFB in cytoskeleton remodeling and the expression of Epithelial-Mesenchymal-Transition markers by Alveolar Epithelial Cells Type II and tests the hypothesis if human alveolar epithelial cells are capable of trans-differentiation and production of pro-fibrotic collagen. Methods: Primary human alveolar epithelial cells type II were extracted from donor tissues and stimulated with TGF? and a TGF?-inhibitor. Transcriptome and pathway analyses as well as validation of results on protein level were conducted. Results: A TGF?-responsive fingerprint was found and investigated for mutual interactions. Interaction modules exhibited enrichment of genes that favor actin cytoskeleton remodeling, differentiation processes and collagen metabolism. Cross-validation of the TGF?-responsive fingerprint in an independent IPF dataset revealed overlap of genes and supported the direction of regulated genes and TGF?-specificity. Conclusions: Primary human alveolar epithelial cells type II seem undergo a TGF?-dependent phenotypic change, exhibit differential expression of EMT markers in vitro and acquire the potential to produce collagen. Electronic supplementary material: The online version of this article (10.1186/s12931-018-0841-9) contains supplementary material, which is available to authorized users.
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