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1000 Titel
  • Bronchoscopic biopsies - a novel source for primary airway epithelial cells in respiratory research
1000 Autor/in
  1. Barbet, Kimberly |
  2. Schmitz, Mona S. |
  3. Westhölter, Dirk |
  4. Kamler, Markus |
  5. Rütten, Stephan |
  6. Thiebes, Anja L. |
  7. Sitek, Barbara |
  8. Bayer, Malte |
  9. Schedel, Michaela |
  10. Reuter, Sebastian |
  11. Darwiche, Kaid |
  12. Luengen, Anja E. |
  13. Taube, Christian |
1000 Verlag BioMed Central
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-12-24
1000 Erschienen in
1000 Quellenangabe
  • 25(1):439
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s12931-024-03060-1 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11669235/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title> <jats:sec> <jats:title>Background</jats:title> <jats:p>Using primary airway epithelial cells (AEC) is essential to mimic more closely different types and stages of lung disease in humans while reducing or even replacing animal experiments. Access to lung tissue remains limited because these samples are generally obtained from patients who undergo lung transplantation for end-stage lung disease or thoracic surgery for (mostly) lung cancer. We investigated whether forceps or cryo biopsies are a viable alternative source of AEC compared to the conventional technique.</jats:p> </jats:sec> <jats:sec> <jats:title>Methods</jats:title> <jats:p>AECs were obtained ex vivo from healthy donor lung tissue using the conventional method and two biopsy procedures (forceps, cryo). The influence of the isolation method on the quality and function of AEC was investigated at different time-points during expansion and differentiation in air-liquid interface cultures. In addition, fully-differentiated AECs were stimulated with house dust mite extract (HDM) to allow functional analyses in an allergic in vitro model. Vitality or differentiation capacity were determined using flow cytometry, scanning electron microscope, periodic acid-Schiff reaction, immunofluorescence staining, and proteomics.</jats:p> </jats:sec> <jats:sec> <jats:title>Results</jats:title> <jats:p>As anticipated, no significant differences between each of the sampling methods were detected for any of the measured outcomes. The proteome composition was comparable for each isolation method, while donor-dependent effects were observed. Treatment with HDM led to minor differences in mucociliary differentiation.</jats:p> </jats:sec> <jats:sec> <jats:title>Conclusions</jats:title> <jats:p>Our findings confirmed the adequacy of these alternative approaches for attaining primary AECs, which can now expand the research for a broader range of lung diseases and for studies at an earlier stage not requiring lung surgery.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Female [MeSH]
lokal Cell Differentiation/physiology [MeSH]
lokal Cryo biopsy
lokal Respiratory Mucosa/pathology [MeSH]
lokal Adult [MeSH]
lokal Biopsy [MeSH]
lokal Humans [MeSH]
lokal Primary airway epithelial cells
lokal Middle Aged [MeSH]
lokal 3R-principle
lokal Animals [MeSH]
lokal Epithelial Cells/metabolism [MeSH]
lokal In vitro disease-model
lokal Male [MeSH]
lokal Research
lokal Respiratory Mucosa/metabolism [MeSH]
lokal Forceps biopsy
lokal Cells, Cultured [MeSH]
lokal Epithelial Cells/pathology [MeSH]
lokal Air-liquid interface
lokal Respiratory Mucosa/cytology [MeSH]
lokal Bronchoscopy/methods [MeSH]
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1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/QmFyYmV0LCBLaW1iZXJseQ==|https://frl.publisso.de/adhoc/uri/U2NobWl0eiwgTW9uYSBTLg==|https://frl.publisso.de/adhoc/uri/V2VzdGjDtmx0ZXIsIERpcms=|https://frl.publisso.de/adhoc/uri/S2FtbGVyLCBNYXJrdXM=|https://frl.publisso.de/adhoc/uri/UsO8dHRlbiwgU3RlcGhhbg==|https://frl.publisso.de/adhoc/uri/VGhpZWJlcywgQW5qYSBMLg==|https://frl.publisso.de/adhoc/uri/U2l0ZWssIEJhcmJhcmE=|https://frl.publisso.de/adhoc/uri/QmF5ZXIsIE1hbHRl|https://frl.publisso.de/adhoc/uri/U2NoZWRlbCwgTWljaGFlbGE=|https://frl.publisso.de/adhoc/uri/UmV1dGVyLCBTZWJhc3RpYW4=|https://frl.publisso.de/adhoc/uri/RGFyd2ljaGUsIEthaWQ=|https://frl.publisso.de/adhoc/uri/THVlbmdlbiwgQW5qYSBFLg==|https://frl.publisso.de/adhoc/uri/VGF1YmUsIENocmlzdGlhbg==
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  1. Universitätsklinikum Essen |
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    1000 Förderer Universitätsklinikum Essen |
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1000 Erstellt am 2025-07-05T10:02:29.400+0200
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1000 Objekt bearb. Tue Aug 19 10:20:23 CEST 2025
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