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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Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Nat Commun
Κύριοι συγγραφείς: 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
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Nature Publishing Group UK 2020
Θέματα:
Article
Διαθέσιμο Online: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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