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A 3-D cell culture system to study epithelia functions using microcarriers.
Jakob, Petra H; Kehrer, Jessica; Flood, Peter; Wiegel, Catharina; Haselmann, Uta; Meissner, Markus; Stelzer, Ernst H K; Reynaud, Emmanuel G.
Afiliación
  • Jakob PH; European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
  • Kehrer J; Wellcome Trust Centre for Molecular Parasitology, Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
  • Flood P; School of Biology and Environmental Science, UCD Science Centre West, University College Dublin, Room 141, Science Center West, Belfield, Dublin 4, Ireland.
  • Wiegel C; European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
  • Haselmann U; European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
  • Meissner M; Wellcome Trust Centre for Molecular Parasitology, Institute of Infection, Immunity and Inflammation, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK.
  • Stelzer EH; Goethe University Frankfurt, Frankfurt am Main, Germany.
  • Reynaud EG; School of Biology and Environmental Science, UCD Science Centre West, University College Dublin, Room 141, Science Center West, Belfield, Dublin 4, Ireland. emmanuel.reynaud@ucd.ie.
Cytotechnology ; 68(5): 1813-25, 2016 Oct.
Article en En | MEDLINE | ID: mdl-26847791
In vitro cell culture models used to study epithelia and epithelial diseases would benefit from the recognition that organs and tissues function in a three-dimensional (3D) environment. This context is necessary for the development of cultures that more realistically resemble in vivo tissues/organs. Our aim was to establish and characterize biologically meaningful 3D models of epithelium. We engineered 3D epithelia cultures using a kidney epithelia cell line (MDCK) and spherical polymer scaffolds. These kidney epithelia were characterized by live microscopy, immunohistochemistry and transmission electron microscopy. Strikingly, the epithelial cells displayed increased physiological relevance; they were extensively polarized and developed a more differentiated phenotype. Using such a growth system allows for direct transmission and fluorescence imaging with few restrictions using wide-field, confocal and Light Sheet Fluorescence Microscopy. We also assessed the wider relevance of this 3D culturing technique with several epithelial cell lines. Finally, we established that these 3D micro-tissues can be used for infection as well as biochemical assays and to study important cellular processes such as epithelial mesenchymal transmission. This new biomimetic model could provide a broadly applicable 3D culture system to study epithelia and epithelia related disorders.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cytotechnology Asunto de la revista: BIOTECNOLOGIA / GENETICA Año: 2016 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cytotechnology Asunto de la revista: BIOTECNOLOGIA / GENETICA Año: 2016 Tipo del documento: Article País de afiliación: Alemania Pais de publicación: Estados Unidos