Mitochondrial Dysfunction in Lung Resident Mesenchymal Stem Cells from Idiopathic Pulmonary Fibrosis Patients

Idiopathic pulmonary fibrosis (IPF) is characterized by an aberrant repair response with uncontrolled turnover of extracellular matrix involving mesenchymal cell phenotypes, where lung resident mesenchymal stem cells (LRMSC) have been supposed to have an important role. However, the contribution of...

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Detalles Bibliográficos
Autores principales: Mercader-Barceló, Josep, Martín-Medina, Aina, Truyols-Vives, Joan, Escarrer-Garau, Gabriel, Elowsson, Linda, Montes-Worboys, Ana, Río-Bocos, Carlos, Muncunill-Farreny, Josep, Velasco-Roca, Julio, Cederberg, Anna, Kadefors, Måns, Molina-Molina, Maria, Westergren-Thorsson, Gunilla, Sala-Llinàs, Ernest
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453747/
https://www.ncbi.nlm.nih.gov/pubmed/37626894
http://dx.doi.org/10.3390/cells12162084

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10453747/
https://www.ncbi.nlm.nih.gov/pubmed/37626894
http://dx.doi.org/10.3390/cells12162084

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