Frontiers in Bioengineering and Biotechnology (Apr 2024)

A miniaturized multicellular platform to mimic the 3D structure of the alveolar-capillary barrier

  • Michela Licciardello,
  • Michela Licciardello,
  • Michela Licciardello,
  • Cecilia Traldi,
  • Cecilia Traldi,
  • Cecilia Traldi,
  • Martina Cicolini,
  • Martina Cicolini,
  • Valentina Bertana,
  • Simone Luigi Marasso,
  • Simone Luigi Marasso,
  • Matteo Cocuzza,
  • Chiara Tonda-Turo,
  • Chiara Tonda-Turo,
  • Chiara Tonda-Turo,
  • Gianluca Ciardelli,
  • Gianluca Ciardelli,
  • Gianluca Ciardelli,
  • Gianluca Ciardelli

DOI
https://doi.org/10.3389/fbioe.2024.1346660
Journal volume & issue
Vol. 12

Abstract

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Several diseases affect the alveoli, and the efficacy of medical treatments and pharmaceutical therapies is hampered by the lack of pre-clinical models able to recreate in vitro the diseases. Microfluidic devices, mimicking the key structural and compositional features of the alveoli, offer several advantages to medium and high-throughput analysis of new candidate therapies. Here, we developed an alveolus-on-a-chip recapitulating the microanatomy of the physiological tissue by including the epithelium, the fibrous interstitial layer and the capillary endothelium. A PDMS device was obtained assembling a top layer and a bottom layer obtained by replica molding. A polycaprolactone/gelatin (PCL-Gel) electrospun membrane was included within the two layers supporting the seeding of 3 cell phenotypes. Epithelial cells were grown on a fibroblast-laden collagen hydrogel located on the top side of the PCL-Gel mats while endothelial cells were seeded on the basolateral side of the membrane. The innovative design of the microfluidic device allows to replicate both cell-cell and cell-extracellular matrix interactions according to the in vivo cell arrangement along with the establishment of physiologically relevant air-liquid interface conditions. Indeed, high cell viability was confirmed for up to 10 days and the formation of a tight endothelial and epithelial barrier was assessed by immunofluorescence assays.

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