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April 27, 2026Biofabrication0 citationsOpen Access

Airway mucosa-derived extracellular matrix bioink for 3D bioprinting of functional airway tissue

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JPJu Young ParkJPJeong Hun ParkJJJinah Jang

Key Points

  • The study aims to develop a bioink from decellularized airway mucosa and evaluate its efficacy in airway tissue engineering.
  • Airway mucosa was processed into a thermo-responsive bioink through decellularization.
  • Human tracheal epithelial cells were cultured on MudECM hydrogels to assess differentiation and function.
  • 3D-printed MudECM scaffolds were implanted in a rat tracheal defect model for functional testing.
  • In vitro studies showed enhanced epithelial differentiation and mucociliary function on MudECM hydrogels.
  • The 3D-printed scaffolds successfully promoted airway tissue regeneration in the rat model.
  • The bioink demonstrated favorable biochemical and mechanical properties for tissue engineering applications.

Abstract

Airway epithelial dysfunction is a hallmark of chronic airway diseases, yet current clinical interventions fail to restore functional airway mucosa. We aimed to develop a bioink derived from airway mucosa-derived decellularized extracellular matrix (MudECM) and evaluate its potential for airway tissue engineering through in vitro and in vivo studies. Airway mucosal tissue was decellularized to preserve tissue-specific ECM components and processed into a thermo-responsive bioink. The biochemical composition, rheological properties, and printability of the bioink were characterized. Human tracheal epithelial cells were cultured on MudECM hydrogels under air-liquid interface conditions to assess epithelial differentiation and mucociliary function. Functional regeneration was tested in a rat tracheal defect model by implanting 3D-printed MudECM scaffolds. A bilayered airway construct was fabricated via 3D bioprinting using MudECM-based bioinks and evaluated for epithelial-stromal organization in vitro.We believe this article will be of particular interest to your readers because airway mucosaderived dECM bioink provides tissue-specific biochemical and mechanical cues that promote mucociliary epithelial regeneration. By enabling both structural and functional restoration in vitro and in vivo, this bioink represents a clinically translatable biomaterial for airway reconstruction. Beyond regenerative graft fabrication, it also offers a robust platform for disease modeling and drug testing in airway research.

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Cite This Study

Park et al. (2026) studied this question.

synapsesocial.com/papers/69eefc6dfede9185760d373ahttps://doi.org/10.1088/1758-5090/ae647d
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