The role of the anti-inflammatory cytokine interleukin-10 in tissue fibrosis

EH Steen, X Wang, S Balaji, MJ Butte… - Advances in wound …, 2020 - liebertpub.com
Significance: Fibrosis is the endpoint of chronic disease in multiple organs, including the
skin, heart, lungs, intestine, liver, and kidneys. Pathologic accumulation of fibrotic tissue …

[HTML][HTML] Fibroblasts in fibrosis: novel roles and mediators

RT Kendall, CA Feghali-Bostwick - Frontiers in pharmacology, 2014 - frontiersin.org
Fibroblasts are the most common cell type of the connective tissues found throughout the
body and the principal source of the extensive extracellular matrix (ECM) characteristic of …

Role of macrophages in acute lung injury and chronic fibrosis induced by pulmonary toxicants

DL Laskin, R Malaviya, JD Laskin - Toxicological Sciences, 2019 - academic.oup.com
A diverse group of toxicants has been identified that cause injury to the lung including gases
(eg, ozone, chlorine), particulates/aerosols (eg, diesel exhaust, fly ash, other combustion …

[PDF][PDF] The chemokine CCL1 triggers an AMFR-SPRY1 pathway that promotes differentiation of lung fibroblasts into myofibroblasts and drives pulmonary fibrosis

S Liu, C Liu, X Lv, B Cui, J Yan, Y Li, K Li, F Hua… - Immunity, 2021 - cell.com
Recruitment of immune cells to the site of inflammation by the chemokine CCL1 is important
in the pathology of inflammatory diseases. Here, we examined the role of CCL1 in …

[HTML][HTML] Wound macrophages as key regulators of repair: origin, phenotype, and function

SK Brancato, JE Albina - The American journal of pathology, 2011 - Elsevier
Recent results call for the reexamination of the phenotype of wound macrophages and their
role in tissue repair. These results include the characterization of distinct circulating …

[HTML][HTML] Pulmonary fibrosis: pathogenesis, etiology and regulation

MS Wilson, TA Wynn - Mucosal immunology, 2009 - Elsevier
Pulmonary fibrosis and architectural remodeling of tissues can severely disrupt lung
function, often with fatal consequences. The etiology of pulmonary fibrotic diseases is varied …

[HTML][HTML] Molecular and cellular mechanisms of pulmonary fibrosis

NW Todd, IG Luzina, SP Atamas - Fibrogenesis & tissue repair, 2012 - Springer
Pulmonary fibrosis is a chronic lung disease characterized by excessive accumulation of
extracellular matrix (ECM) and remodeling of the lung architecture. Idiopathic pulmonary …

The pathogenesis of pulmonary fibrosis: a moving target

WA Wuyts, C Agostini, KM Antoniou… - European …, 2013 - Eur Respiratory Soc
Pulmonary fibrosis is the end stage of many diffuse parenchymal lung diseases. It is
characterised by excessive matrix formation leading to destruction of the normal lung …

The immunology of fibrosis

G Wick, C Grundtman, C Mayerl… - Annual review of …, 2013 - annualreviews.org
Fibrosis is the production of excessive amounts of connective tissue, ie, scar formation, in
the course of reactive and reparative processes. Fibrosis develops as a consequence of …

Molecular targets in pulmonary fibrosis: the myofibroblast in focus

CJ Scotton, RC Chambers - Chest, 2007 - Elsevier
Idiopathic pulmonary fibrosis (IPF) is one of a group of interstitial lung diseases that are
characterized by excessive matrix deposition and destruction of the normal lung …