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Generation of an alveolar epithelial type II cell line from induced pluripotent stem cells.
Tamò, Luca; Hibaoui, Youssef; Kallol, Sampada; Alves, Marco P; Albrecht, Christiane; Hostettler, Katrin E; Feki, Anis; Rougier, Jean-Sebastien; Abriel, Hugues; Knudsen, Lars; Gazdhar, Amiq; Geiser, Thomas.
Afiliação
  • Tamò L; Department of Pulmonary Medicine, University Hospital Bern, University of Bern , Bern, Switzerland.
  • Hibaoui Y; Graduate School for Cellular and Biomedical Sciences, University of Bern , Bern, Switzerland.
  • Kallol S; Department of Biomedical Research, University of Bern , Bern, Switzerland.
  • Alves MP; Department of Gynecology and Obstetrics, University Hospital Geneva , Geneva, Switzerland.
  • Albrecht C; Graduate School for Cellular and Biomedical Sciences, University of Bern , Bern, Switzerland.
  • Hostettler KE; Institute of Biochemistry and Molecular Medicine, University of Bern , Bern, Switzerland.
  • Feki A; Department of Pediatric Pneumology, University Hospital Bern , Bern, Switzerland.
  • Rougier JS; Department of Infectious Diseases and Pathobiology, Vetsuisse Faculty, University of Bern , Bern, Switzerland.
  • Abriel H; Institute of Virology and Immunology , Bern , Switzerland.
  • Knudsen L; Institute of Biochemistry and Molecular Medicine, University of Bern , Bern, Switzerland.
  • Gazdhar A; Swiss National Center of Competence in Research, National Centre of Competence in Research TransCure, University of Bern , Bern , Switzerland.
  • Geiser T; Clinics of Respiratory Medicine, University Hospital Basel, University of Basel , Basel, Switzerland.
Am J Physiol Lung Cell Mol Physiol ; 315(6): L921-L932, 2018 12 01.
Article em En | MEDLINE | ID: mdl-30211653
ABSTRACT
Differentiation of primary alveolar type II epithelial cells (AEC II) to AEC type I in culture is a major barrier in the study of the alveolar epithelium in vitro. The establishment of an AEC II cell line derived from induced pluripotent stem cells (iPSC) represents a novel opportunity to study alveolar epithelial cell biology, for instance, in the context of lung injury, fibrosis, and repair. In the present study, we generated long-lasting AEC II from iPSC (LL-iPSC-AEC II). LL-iPSC-AEC II displayed morphological characteristics of AEC II, including growth in a cobblestone monolayer, the presence of lamellar bodies, and microvilli, as shown by electron microscopy. Also, LL-iPSC-AEC II expressed AEC type II proteins, such as cytokeratin, surfactant protein C, and LysoTracker DND 26 (a marker for lamellar bodies). Furthermore, the LL-iPSC-AEC II exhibited functional properties of AEC II by an increase of transepithelial electrical resistance over time, secretion of inflammatory mediators in biologically relevant quantities (IL-6 and IL-8), and efficient in vitro alveolar epithelial wound repair. Consistent with the AEC II phenotype, the cell line showed the ability to uptake and release surfactant protein B, to secrete phospholipids, and to differentiate into AEC type I. In summary, we established a long-lasting, but finite AEC type II cell line derived from iPSC as a novel cellular model to study alveolar epithelial cell biology in lung health and disease.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Epiteliais Alveolares / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Am J Physiol Lung Cell Mol Physiol Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Células Epiteliais Alveolares / Células-Tronco Pluripotentes Induzidas Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Revista: Am J Physiol Lung Cell Mol Physiol Ano de publicação: 2018 Tipo de documento: Article