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METHODS article

Front. Bioeng. Biotechnol.

Sec. Tissue Engineering and Regenerative Medicine

Generation of a human vascularized 3D airway model replicating native mucosal heterogeneity

Provisionally accepted
  • Department of Biohybrid & Medical Textiles, Institute of Applied Medical Engineering, Helmholtz Institute, RWTH Aachen University, Aachen, Germany

The final, formatted version of the article will be published soon.

In vitro models of the human airway are essential to study respiratory diseases and test potential therapeutics while reducing animal testing. Current models often use two-dimensional culture conditions rather than replicating the physiological 3D environment and do not allow direct cell-cell interactions between the diverse cell types found in the mucosa. Here, we provide a detailed step-by-step instruction for reproducibly generating a complex tri-culture model, which can be used to investigate the human airway environment in health and disease. The model is fabricated by preparing an epithelialized fibrin hydrogel with embedded endothelial and stromal cells. To assure complete differentiation into a mucociliary phenotype, samples are maintained at air-liquid interface (ALI) for 28 days. Afterwards, morphology and functionality can be validated using downstream analysis techniques such as immunohisto-and cytochemistry, electron microscopy, ciliary beating frequency analysis, measurement of mucociliary clearance and RNA isolation. After four weeks of maturation, a well-differentiated pseudostratified epithelium comprising basal, multiciliated and secretory cells is developed. We also observe a physiological ciliary beating frequency, mucus production and a functional particle clearance. Inside the hydrogel, endothelial cells form a three-dimensional network of vascular structures. These features make our model ideal for replicating human mucosal heterogeneity, especially compared to airway models using tumor-derived or immortalized cell lines, monocultures or rigid substrates. Hence, this protocol paves the way for fellow researchers to achieve robust airway in vitro modeling that can be performed in a standard cell culture lab without the need for extraordinary equipment or specialized expertise.

Keywords: 3D in vitro model, air-liquid interface, Cilia, differentiation, human airway epithelium, Hydrogel, tri-culture, vascularization

Received: 05 Dec 2025; Accepted: 26 Jan 2026.

Copyright: © 2026 Kubiza, Gonzalez-Rubio, Jockenhoevel and Thiebes. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Anja Lena Thiebes

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