4.8 Article

Reconstituting Organ-Level Lung Functions on a Chip

Journal

SCIENCE
Volume 328, Issue 5986, Pages 1662-1668

Publisher

AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1188302

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Funding

  1. NIH [R01-ES016665]
  2. American Heart Association [0835618D]
  3. Department of Defense [W81XWH-05-1-0115]
  4. Wyss Institute for Biologically Inspired Engineering at Harvard University
  5. Wyss Technology Development Fellowship

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Here, we describe a biomimetic microsystem that reconstitutes the critical functional alveolar-capillary interface of the human lung. This bioinspired microdevice reproduces complex integrated organ-level responses to bacteria and inflammatory cytokines introduced into the alveolar space. In nanotoxicology studies, this lung mimic revealed that cyclic mechanical strain accentuates toxic and inflammatory responses of the lung to silica nanoparticles. Mechanical strain also enhances epithelial and endothelial uptake of nanoparticulates and stimulates their transport into the underlying microvascular channel. Similar effects of physiological breathing on nanoparticle absorption are observed in whole mouse lung. Mechanically active organ-on-a-chip microdevices that reconstitute tissue-tissue interfaces critical to organ function may therefore expand the capabilities of cell culture models and provide low-cost alternatives to animal and clinical studies for drug screening and toxicology applications.

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