Your browser doesn't support javascript.
Lung-on-a-Chip Models of the Lung Parenchyma.
Zamprogno, Pauline; Schulte, Jan; Ferrari, Dario; Rechberger, Karin; Sengupta, Arunima; van Os, Lisette; Weber, Tobias; Zeinali, Soheila; Geiser, Thomas; Guenat, Olivier T.
  • Zamprogno P; Organs-on-Chip Technologies Laboratory, ARTORG Center, University of Bern, Bern, Switzerland.
  • Schulte J; Organs-on-Chip Technologies Laboratory, ARTORG Center, University of Bern, Bern, Switzerland.
  • Ferrari D; Organs-on-Chip Technologies Laboratory, ARTORG Center, University of Bern, Bern, Switzerland.
  • Rechberger K; Organs-on-Chip Technologies Laboratory, ARTORG Center, University of Bern, Bern, Switzerland.
  • Sengupta A; Organs-on-Chip Technologies Laboratory, ARTORG Center, University of Bern, Bern, Switzerland.
  • van Os L; Organs-on-Chip Technologies Laboratory, ARTORG Center, University of Bern, Bern, Switzerland.
  • Weber T; Organs-on-Chip Technologies Laboratory, ARTORG Center, University of Bern, Bern, Switzerland.
  • Zeinali S; Organs-on-Chip Technologies Laboratory, ARTORG Center, University of Bern, Bern, Switzerland.
  • Geiser T; Department of Pulmonary Medicine, University Hospital of Bern, Bern, Switzerland.
  • Guenat OT; Organs-on-Chip Technologies Laboratory, ARTORG Center, University of Bern, Bern, Switzerland. olivier.guenat@unibe.ch.
Adv Exp Med Biol ; 1413: 191-211, 2023.
Article in English | MEDLINE | ID: covidwho-2327320
ABSTRACT
Since the publication of the first lung-on-a-chip in 2010, research has made tremendous progress in mimicking the cellular environment of healthy and diseased alveoli. As the first lung-on-a-chip products have recently reached the market, innovative solutions to even better mimic the alveolar barrier are paving the way for the next generation lung-on-chips. The original polymeric membranes made of PDMS are being replaced by hydrogel membranes made of proteins from the lung extracellular matrix, whose chemical and physical properties exceed those of the original membranes. Other aspects of the alveolar environment are replicated, such as the size of the alveoli, their three-dimensional structure, and their arrangement. By tuning the properties of this environment, the phenotype of alveolar cells can be tuned, and the functions of the air-blood barrier can be reproduced, allowing complex biological processes to be mimicked. Lung-on-a-chip technologies also provide the possibility of obtaining biological information that was not possible with conventional in vitro systems. Pulmonary edema leaking through a damaged alveolar barrier and barrier stiffening due to excessive accumulation of extracellular matrix proteins can now be reproduced. Provided that the challenges of this young technology are overcome, there is no doubt that many application areas will benefit greatly.
Subject(s)
Keywords

Full text: Available Collection: International databases Database: MEDLINE Main subject: Pulmonary Alveoli / Lung Language: English Journal: Adv Exp Med Biol Year: 2023 Document Type: Article Affiliation country: 978-3-031-26625-6_10

Similar

MEDLINE

...
LILACS

LIS


Full text: Available Collection: International databases Database: MEDLINE Main subject: Pulmonary Alveoli / Lung Language: English Journal: Adv Exp Med Biol Year: 2023 Document Type: Article Affiliation country: 978-3-031-26625-6_10