The role of the anti-inflammatory cytokine interleukin-10 in tissue fibrosis
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 …
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 …
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
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 …
(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
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 …
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 …
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 …
function, often with fatal consequences. The etiology of pulmonary fibrotic diseases is varied …
[HTML][HTML] Molecular and cellular mechanisms of pulmonary fibrosis
Pulmonary fibrosis is a chronic lung disease characterized by excessive accumulation of
extracellular matrix (ECM) and remodeling of the lung architecture. Idiopathic pulmonary …
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 …
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 …
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 …
characterized by excessive matrix deposition and destruction of the normal lung …