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

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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Bibliographic Details
Main Authors: Josep Mercader-Barceló, Aina Martín-Medina, Joan Truyols-Vives, Gabriel Escarrer-Garau, Linda Elowsson, Ana Montes-Worboys, Carlos Río-Bocos, Josep Muncunill-Farreny, Julio Velasco-Roca, Anna Cederberg, Måns Kadefors, Maria Molina-Molina, Gunilla Westergren-Thorsson, Ernest Sala-Llinàs
Format: Article
Language:English
Published: MDPI AG 2023-08-01
Series:Cells
Subjects:
idiopathic pulmonary fibrosis
lung resident mesenchymal stem cell
mitochondria
oxidative phosphorylation
mitophagy
apoptosis
Online Access:https://www.mdpi.com/2073-4409/12/16/2084

Internet

https://www.mdpi.com/2073-4409/12/16/2084

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