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Development of a physiomimetic model of acute respiratory distress syndrome by using ECM hydrogels and organ-on-a-chip devices

Marhuenda, Esther (author)
Carlos III Health Institute,University of Barcelona
Villarino, Alvaro (author)
University of Barcelona
Narciso, Maria (author)
Barcelona Institute of Science and Technology,University of Barcelona
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Elowsson, Linda (author)
Lund University,Lunds universitet,Lungbiologi,Forskargrupper vid Lunds universitet,Lung Biology,Lund University Research Groups
Almendros, Isaac (author)
University of Barcelona,Carlos III Health Institute,Institutd' Investigacions Biomèdiques August Pi iSunyer (IDIBAPS)
Westergren-Thorsson, Gunilla (author)
Lund University,Lunds universitet,Lungbiologi,Forskargrupper vid Lunds universitet,Lund University Bioimaging Center,Medicinska fakulteten,Lung Biology,Lund University Research Groups,Faculty of Medicine
Farré, Ramon (author)
Carlos III Health Institute,University of Barcelona,Institutd' Investigacions Biomèdiques August Pi iSunyer (IDIBAPS)
Gavara, Núria (author)
Barcelona Institute of Science and Technology,Carlos III Health Institute,University of Barcelona
Otero, Jorge (author)
University of Barcelona,Carlos III Health Institute,Barcelona Institute of Science and Technology
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 (creator_code:org_t)
2022-09-02
2022
English.
In: Frontiers in Pharmacology. - : Frontiers Media SA. - 1663-9812. ; 13
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • Acute Respiratory Distress Syndrome is one of the more common fatal complications in COVID-19, characterized by a highly aberrant inflammatory response. Pre-clinical models to study the effect of cell therapy and anti-inflammatory treatments have not comprehensively reproduced the disease due to its high complexity. This work presents a novel physiomimetic in vitro model for Acute Respiratory Distress Syndrome using lung extracellular matrix-derived hydrogels and organ-on-a-chip devices. Monolayres of primary alveolar epithelial cells were cultured on top of decellullarized lung hydrogels containing primary lung mesenchymal stromal cells. Then, cyclic stretch was applied to mimic breathing, and an inflammatory response was induced by using a bacteriotoxin hit. Having simulated the inflamed breathing lung environment, we assessed the effect of an anti-inflammatory drug (i.e., dexamethasone) by studying the secretion of the most relevant inflammatory cytokines. To better identify key players in our model, the impact of the individual factors (cyclic stretch, decellularized lung hydrogel scaffold, and the presence of mesenchymal stromal cells) was studied separately. Results showed that developed model presented a more reduced inflammatory response than traditional models, which is in line with what is expected from the response commonly observed in patients. Further, from the individual analysis of the different stimuli, it was observed that the use of extracellular matrix hydrogels obtained from decellularized lungs had the most significant impact on the change of the inflammatory response. The developed model then opens the door for further in vitro studies with a better-adjusted response to the inflammatory hit and more robust results in the test of different drugs or cell therapy.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Lungmedicin och allergi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Respiratory Medicine and Allergy (hsv//eng)

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