Fibroblast–matrix interplay: Nintedanib and pirfenidone modulate the effect of IPF fibroblast‐conditioned matrix on normal fibroblast phenotype

G Epstein Shochet, L Wollin, D Shitrit - Respirology, 2018 - Wiley Online Library
Background and objective Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease
with poor prognosis. Activated fibroblasts are the key effector cells in fibrosis, producing …

[HTML][HTML] Pirfenidone and nintedanib modulate properties of fibroblasts and myofibroblasts in idiopathic pulmonary fibrosis

ST Lehtonen, A Veijola, H Karvonen… - Respiratory …, 2016 - Springer
Background Idiopathic pulmonary fibrosis (IPF) is an incurable lung disease with a poor
prognosis. Fibroblasts and myofibroblasts are the key cells in the fibrotic process. Recently …

[HTML][HTML] Fibroblast–matrix cross-talk in idiopathic pulmonary fibrosis: cross-links at the crossroads

P Bitterman - American journal of respiratory cell and molecular …, 2018 - atsjournals.org
Remodeling of the extracellular matrix (ECM) is both a cause and consequence of human
diseases ranging from organ fibrosis to cancer (1). Idiopathic pulmonary fibrosis (IPF) is a …

[HTML][HTML] Hypoxia inducible factor 1A supports a pro-fibrotic phenotype loop in idiopathic pulmonary fibrosis

G Epstein Shochet, B Bardenstein-Wald… - International Journal of …, 2021 - mdpi.com
Idiopathic pulmonary fibrosis (IPF) is a progressive lung disease with poor prognosis. The
IPF-conditioned matrix (IPF-CM) system enables the study of matrix–fibroblast interplay …

A novel antifibrotic mechanism of nintedanib and pirfenidone. Inhibition of collagen fibril assembly

L Knüppel, Y Ishikawa, M Aichler… - American journal of …, 2017 - atsjournals.org
Idiopathic pulmonary fibrosis (IPF) is characterized by excessive deposition of extracellular
matrix, in particular, collagens. Two IPF therapeutics, nintedanib and pirfenidone, decelerate …

[HTML][HTML] Prolonged Scar-in-a-Jar: an in vitro screening tool for anti-fibrotic therapies using biomarkers of extracellular matrix synthesis

SR Rønnow, RQ Dabbagh, F Genovese… - Respiratory …, 2020 - Springer
Background Idiopathic pulmonary fibrosis (IPF) is a rapidly progressing disease with
challenging management. To find novel effective therapies, better preclinical models are …

Fibroblast heterogeneity in pulmonary fibrosis: a new target for therapeutics development?

K Tsoyi, IO Rosas - European Respiratory Journal, 2024 - Eur Respiratory Soc
Extract Idiopathic pulmonary fibrosis (IPF) is a chronic interstitial lung disease with unknown
aetiology [1]. The prevalence of this devastating disease continues to increase, affecting …

Endothelial colony-forming cells do not participate to fibrogenesis in a bleomycin-induced pulmonary fibrosis model in nude mice

A Blandinières, T Gille, J Sadoine, I Bièche… - Stem Cell Reviews and …, 2018 - Springer
Idiopathic pulmonary fibrosis (IPF) is a devastating lung disease characterized by fibroblast
proliferation, extracellular matrix deposition, destruction of pulmonary alveolar architecture …

[HTML][HTML] Idiopathic pulmonary fibrosis is associated with endothelial to mesenchymal transition

D Nataraj, A Ernst, R Kalluri - American journal of respiratory cell …, 2010 - atsjournals.org
Idiopathic pulmonary fibrosis (IPF) affects over 500,000 people in the United States and
Europe alone. The disease is characterized by progressive obliteration of normal alveolar …

[HTML][HTML] Differential effects of Nintedanib and Pirfenidone on lung alveolar epithelial cell function in ex vivo murine and human lung tissue cultures of pulmonary …

M Lehmann, L Buhl, HN Alsafadi, S Klee… - Respiratory …, 2018 - Springer
Background Idiopathic pulmonary fibrosis (IPF) is a fatal interstitial lung disease. Repetitive
injury and reprogramming of the lung epithelium are thought to be critical drivers of disease …