Angiogenesis may be an important factor in the development of fibrotic lung disease. Prior studies have strongly suggested a role for angiogenic vascular remodeling in pulmonary fibrosis, and emerging evidence indicates that new vessel formation is critical in airway fibrosis. Bronchiolitis obliterans syndrome is a fibrotic occlusion of distal airways that is largely responsible for the morbidity and mortality of patients after lung transplantation. In this issue, Belperio et al. demonstrate a role for CXC chemokine receptor 2 in the regulation of angiogenesis-mediated airway fibroproliferation. By integrating an understanding of neovascularization into the study of events that occur between inflammation and fibrosis, it becomes increasingly possible to rationally design therapies that can halt conditions of maladaptive fibrosis.
Ivor S. Douglas, Mark R. Nicolls
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Targeting Interleukin-10 Restores Graft Microvascular Supply and Airway Epithelium in Rejecting Allografts
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International journal of molecular sciences | 2022 |
STAT3-mediated IGF-2 secretion in the tumour microenvironment elicits innate resistance to anti-IGF-1R antibody
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Nature Communications | 2015 |
An Acvr1 R206H knock-in mouse has fibrodysplasia ossificans progressiva
SA Chakkalakal, D Zhang, AL Culbert, MR Convente, RJ Caron, AC Wright, AD Maidment, FS Kaplan, EM Shore |
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Green Tea Epigallo-Catechin-Galleate Ameliorates the Development of Obliterative Airway Disease
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C Knoop, M Estenne |
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Stem Cells | 2009 |
Vascular biology and pathobiology of the liver: Report of a single-topic symposium
Y Iwakiri, M Grisham, V Shah |
Hepatology | 2008 |
The role of chemokines during herpes simplex virus-1 infection
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Frontiers in bioscience : a journal and virtual library | 2008 |