Inhalation of lung spheroid cell secretome and exosomes promotes lung repair in pulmonary fibrosis

Idiopathic pulmonary fibrosis (IPF) is a fatal and incurable form of interstitial lung disease in which persistent injury results in scar tissue formation. As fibrosis thickens, the lung tissue loses the ability to facilitate gas exchange and provide cells with needed oxygen. Currently, IPF has few...

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Publicat a:Nat Commun
Autors principals: Dinh, Phuong-Uyen C., Paudel, Dipti, Brochu, Hayden, Popowski, Kristen D., Gracieux, M. Cyndell, Cores, Jhon, Huang, Ke, Hensley, M. Taylor, Harrell, Erin, Vandergriff, Adam C., George, Arianna K., Barrio, Raina T., Hu, Shiqi, Allen, Tyler A., Blackburn, Kevin, Caranasos, Thomas G., Peng, Xinxia, Schnabel, Lauren V., Adler, Kenneth B., Lobo, Leonard J., Goshe, Michael B., Cheng, Ke
Format: Artigo
Idioma:Inglês
Publicat: Nature Publishing Group UK 2020
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Article
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC7048814/
https://ncbi.nlm.nih.gov/pubmed/32111836
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41467-020-14344-7
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