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The effect of age and emphysematous and fibrotic injury on the re-cellularization of de-cellularized lungs

  • Dino Sokocevic
  • , Nicholas R. Bonenfant
  • , Darcy E. Wagner
  • , Zachary D. Borg
  • , Melissa J. Lathrop
  • , Ying Wai Lam
  • , Bin Deng
  • , Michael J. DeSarno
  • , Taka Ashikaga
  • , Roberto Loi
  • , Andrew M. Hoffman
  • , Daniel J. Weiss*
  • *Corresponding author for this work
  • University of Vermont
  • University of Cagliari
  • Tufts University

Research output: Contribution to journalArticlepeer-review

94 Scopus citations

Abstract

Use of de-cellularized cadaveric lungs as 3-dimensional scaffolds for ex vivo lung tissue generation offers a new potential therapeutic approach for clinical lung transplantation. However, it is likely that some of the available cadaveric human lungs may be from older donors or from donors with previously existing structural lung diseases such as emphysema or pulmonary fibrosis. It is not known whether these lungs will be suitable for either de-cellularization or re-cellularization. To investigate this, we assessed the effects of advanced age, representative emphysematous and fibrotic injuries, and the combination of advanced age and emphysematous injury and found significant differences both in histologic appearance and in the retention of extracellular matrix (ECM) and other proteins, as assessed by immunohistochemistry and mass spectrometry, between the different conditions. However, despite these differences, binding, retention and growth of bone marrow-derived mesenchymal stromal cells (MSCs) over a 1-month period following intratracheal inoculation were similar between the different experimental conditions. In contrast, significant differences occurred in the growth of C10 mouse lung epithelial cells between the different conditions. Therefore, age, lung injury, and the cell type used for re-cellularization may significantly impact the usefulness of de-cellularized whole lungs for ex vivo lung tissue regeneration.

Original languageEnglish
Pages (from-to)3256-3269
Number of pages14
JournalBiomaterials
Volume34
Issue number13
DOIs
StatePublished - Apr 2013
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Acellular matrix
  • Age
  • Epithelial cell
  • Extracellular matrix (ECM)
  • Lung
  • Mesenchymal stem cell

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