Capturing the Onset of Bacterial Pulmonary Infection in Acini-On-Chips.
Acinar Cells
/ cytology
Cell Culture Techniques
/ instrumentation
Cell Line, Transformed
Coculture Techniques
Dimethylpolysiloxanes
/ chemistry
High-Throughput Screening Assays
Humans
Interleukin-8
/ biosynthesis
Lab-On-A-Chip Devices
Lipopolysaccharides
/ pharmacology
Microtechnology
/ instrumentation
Models, Biological
Respiratory Mucosa
/ cytology
THP-1 Cells
epithelial barrier
in vitro assays
microfluidics
organ-on-chip
pulmonary infection
Journal
Advanced biosystems
ISSN: 2366-7478
Titre abrégé: Adv Biosyst
Pays: Germany
ID NLM: 101711718
Informations de publication
Date de publication:
09 2019
09 2019
Historique:
received:
26
02
2019
revised:
30
06
2019
entrez:
11
7
2020
pubmed:
11
7
2020
medline:
20
9
2020
Statut:
ppublish
Résumé
Bacterial invasion of the respiratory system leads to complex immune responses. In the deep alveolar regions, the first line of defense includes foremost the alveolar epithelium, the surfactant-rich liquid lining, and alveolar macrophages. Typical in vitro models come short of mimicking the complexity of the airway environment in the onset of airway infection; among others, they neither capture the relevant anatomical features nor the physiological flows innate of the acinar milieu. Here, novel microfluidic-based acini-on-chips that mimic more closely the native acinar airways at a true scale with an anatomically inspired, multigeneration alveolated tree are presented and an inhalation-like maneuver is delivered. Composed of human alveolar epithelial lentivirus immortalized cells and macrophages-like human THP-1 cells at an air-liquid interface, the models maintain critically an epithelial barrier with immune function. To demonstrate, the usability and versatility of the platforms, a realistic inhalation exposure assay mimicking bacterial infection is recapitulated, whereby the alveolar epithelium is exposed to lipopolysaccharides droplets directly aerosolized and the innate immune response is assessed by monitoring the secretion of IL8 cytokines. These efforts underscore the potential to deliver advanced in vitro biosystems that can provide new insights into drug screening as well as acute and subacute toxicity assays.
Identifiants
pubmed: 32648651
doi: 10.1002/adbi.201900026
pmc: PMC7611792
mid: EMS136011
doi:
Substances chimiques
Dimethylpolysiloxanes
0
Interleukin-8
0
Lipopolysaccharides
0
baysilon
63148-62-9
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e1900026Subventions
Organisme : European Research Council
ID : 677772
Pays : International
Informations de copyright
© 2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
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