Update of Aging Hallmarks in Idiopathic Pulmonary Fibrosis

Update of Aging Hallmarks in Idiopathic Pulmonary Fibrosis

Idiopathic Pulmonary Fibrosis (IPF) is an epithelial-driven interstitial lung disease of unknown etiology characterized by the excessive proliferation of fibroblast populations that synthesize large amounts of extracellular matrix. In this devastating disorder, all aging hallmarks appear prematurely...

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Bibliographic Details
Main Authors: Ana Lilia Torres-Machorro, Ángeles García-Vicente, Marco Espina-Ordoñez, Erika Luis-García, Miguel Negreros, Iliana Herrera, Carina Becerril, Fernanda Toscano, Jose Cisneros, Mariel Maldonado
Format: Article
Language:English
Published: MDPI AG 2025-02-01
Series:Cells
Subjects:
idiopathic pulmonary fibrosis
aging hallmarks
mechanical alterations
dysbiosis
inflammaging
alternative splicing
Online Access:https://www.mdpi.com/2073-4409/14/3/222

Internet

https://www.mdpi.com/2073-4409/14/3/222

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