In vitro engineering of the lung alveolus

Leiby, K. L.; Yuan, Y.; Ng, R.; Raredon, M. S. B.; Adams, T. S.; Baevova, P.; Hirschi, K. K.; Campbell, S. G.; Kaminski, N.; Herzog, E. L.; Niklason, L. E.

doi:10.1101/2022.03.13.484143

bioRxiv · 10.1101/2022.03.13.484143

In vitro engineering of the lung alveolus

Leiby, K. L.·Yuan, Y.·Ng, R.·Raredon, M. S. B.·Adams, T. S.·Baevova, P.·Hirschi, K. K.·Campbell, S. G.·Kaminski, N.·Herzog, E. L.·Niklason, L. E.

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Abstract

Therapeutic lung regeneration is predicated upon successful reconstitution of lung alveoli, the functional units of gas exchange. Here, we identify requisite multimodal cues that are critical to reconstructing the alveolar epithelium and alveoli in lung scaffolds. Alveolar reconstruction in vitro is divided into several distinct phases. In the first phase, endothelial cells coordinate with fibroblasts and select exogenous factors to promote alveolar scaffold population with surfactant-secreting alveolar epithelial type 2 cells (AEC2s). After formation of organized epithelial alveolar-like structures, subsequent withdrawal of Wnt and FGF agonism synergizes with tidal-level mechanical strain to induce differentiation of AEC2s to squamous type 1 AECs (AEC1s) in cultured alveoli, in situ. These results outline a rational strategy to engineer an alveolus of AEC2s and AEC1s contained within epithelial-mesenchymal-endothelial units, and reveal the critical interplay amongst biochemical, cellular, and mechanical niche cues within the reconstituting alveolus.

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Leiby, K. L., Yuan, Y., Ng, R., Raredon, M. S. B., Adams, T. S., Baevova, P., Hirschi, K. K., Campbell, S. G., Kaminski, N., Herzog, E. L., Niklason, L. E.. 2022-03-14. In vitro engineering of the lung alveolus. https://doi.org/10.1101/2022.03.13.484143

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