Lung Extracellular Matrix Hydrogels Enhance Preservation of Type II Phenotype in Primary Alveolar Epithelial Cells

One of the main limitations of in vitro studies on lung diseases is the difficulty of maintaining the type II phenotype of alveolar epithelial cells in culture. This fact has previously been related to the translocation of the mechanosensing Yes-associated protein (YAP) to the nuclei and Rho signali...

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Bibliographic Details
Authors: Marhuenda, Esther|||0000-0001-9467-0459, Villarino, Alvaro, Narciso, Maria Leonor|||0000-0002-4994-1691, Camprubí-Rimblas, Marta|||0000-0002-4085-5324, Farré, Ramon|||0000-0002-9084-7824, Gavara, Núria|||0000-0002-7666-110X, Artigas Raventós, Antoni|||0000-0002-8029-1017, Almendros, Isaac|||0000-0002-1998-9379, Otero, Jorge
Format: article
Publication Date:2022
Country:España
Institution:Universitat Autònoma de Barcelona
Repository:Dipòsit Digital de Documents de la UAB
Language:English
OAI Identifier:oai:ddd.uab.cat:282917
Online Access:https://ddd.uab.cat/record/282917
https://dx.doi.org/urn:doi:10.3390/ijms23094888
Access Level:Open access
Keyword:Alveolar cells
Extracellular matrix
Hydrogels
Type II phenotype
YAP
Description
Summary:One of the main limitations of in vitro studies on lung diseases is the difficulty of maintaining the type II phenotype of alveolar epithelial cells in culture. This fact has previously been related to the translocation of the mechanosensing Yes-associated protein (YAP) to the nuclei and Rho signaling pathway. In this work, we aimed to culture and subculture primary alveolar type II cells on extracellular matrix lung-derived hydrogels to assess their suitability for phenotype maintenance. Cells cultured on lung hydrogels formed monolayers and maintained type II phenotype for a longer time as compared with those conventionally cultured. Interestingly, cells successfully grew when they were subsequently cultured on a dish. Moreover, cells cultured on a plate showed the active form of the YAP protein and the formation of stress fibers and focal adhesions. The results of chemically inhibiting the Rho pathway strongly suggest that this is one of the mechanisms by which the hydrogel promotes type II phenotype maintenance. These results regarding protein expression strongly suggest that the chemical and biophysical properties of the hydrogel have a considerable impact on the transition from ATII to ATI phenotypes. In conclusion, culturing primary alveolar epithelial cells on lung ECM-derived hydrogels may facilitate the prolonged culturing of these cells, and thus help in the research on lung diseases.