Collagen breakdown during acute lung injury
- PMID: 2463695
- PMCID: PMC461375
- DOI: 10.1136/thx.43.7.562
Collagen breakdown during acute lung injury
Abstract
Injury to the capillary endothelium and to alveolar epithelial cells of the lung may result in damage to the underlying collagen of the extracellular matrix. To examine this possibility, whole body irradiation, bleomycin injections, and exposure to hyperoxia were used to induce various types of lung damage in mice. The morphology of the lung and the cellular and protein content of bronchoalveolar lavage fluid were used to assess injury. Collagen breakdown was assessed from the hydroxyproline concentrations in bronchoalveolar lavage fluid. When lung cell injury was observed, protein leaked in to alveoli and hydroxyproline was detected in bronchoalveolar lavage fluid. An increase in hydroxyproline followed endothelial damage by irradiation and was greatly increased when type 1 epithelial cell necrosis also occurred after bleomycin injection or hyperoxia. Maximal concentrations of hydroxyproline occurred in mice showing respiratory distress after six days of hyperoxia. Concentrations returned to zero during the subsequent phases of cell regeneration and fibrosis seen after bleomycin injection and irradiation. There was little change in the cellular components of bronchoalveolar lavage fluid at any time. The results indicate that collagen breakdown occurs during acute lung injury and can be quantified in terms of the hydroxyproline concentration in lavage fluid. Such a change in the extracellular matrix might influence the subsequent division and differentiation of regenerating cells during repair.
Similar articles
-
High-dose inhaled nitric oxide and hyperoxia increases lung collagen accumulation in piglets.Biol Neonate. 2000 Oct;78(3):198-206. doi: 10.1159/000014271. Biol Neonate. 2000. PMID: 11044769
-
Cathepsin S deficiency confers protection from neonatal hyperoxia-induced lung injury.Am J Respir Crit Care Med. 2007 Oct 15;176(8):778-85. doi: 10.1164/rccm.200704-519OC. Epub 2007 Aug 2. Am J Respir Crit Care Med. 2007. PMID: 17673697 Free PMC article.
-
C-C chemokine receptor 2 (CCR2) deficiency improves bleomycin-induced pulmonary fibrosis by attenuation of both macrophage infiltration and production of macrophage-derived matrix metalloproteinases.J Pathol. 2004 Dec;204(5):594-604. doi: 10.1002/path.1667. J Pathol. 2004. PMID: 15538737
-
Mesothelial cell proliferation: a nonspecific response to lung injury associated with fibrosis.Am J Respir Cell Mol Biol. 1994 Mar;10(3):253-8. doi: 10.1165/ajrcmb.10.3.7509611. Am J Respir Cell Mol Biol. 1994. PMID: 7509611
-
Matrix metalloproteinases in lung repair.Eur Respir J Suppl. 2003 Sep;44:36s-38s. doi: 10.1183/09031936.03.00001203. Eur Respir J Suppl. 2003. PMID: 14582900 Review. No abstract available.
Cited by
-
Matrix metalloproteinase-9 expression in congenital diaphragmatic hernia during mechanical ventilation.Surg Today. 2005;35(7):524-9. doi: 10.1007/s00595-004-2969-0. Surg Today. 2005. PMID: 15976947
-
Epithelium-specific deletion of TGF-β receptor type II protects mice from bleomycin-induced pulmonary fibrosis.J Clin Invest. 2011 Jan;121(1):277-87. doi: 10.1172/JCI42090. Epub 2010 Dec 6. J Clin Invest. 2011. PMID: 21135509 Free PMC article.
-
Protective effect of Mimosa pudica L. in an L-arginine model of acute necrotising pancreatitis in rats.J Nat Med. 2016 Jul;70(3):423-34. doi: 10.1007/s11418-016-0991-3. Epub 2016 May 10. J Nat Med. 2016. PMID: 27164910
-
GLP-1 receptor agonist ameliorates experimental lung fibrosis.Sci Rep. 2020 Oct 22;10(1):18091. doi: 10.1038/s41598-020-74912-1. Sci Rep. 2020. PMID: 33093510 Free PMC article.
-
ADAM9 is a novel product of polymorphonuclear neutrophils: regulation of expression and contributions to extracellular matrix protein degradation during acute lung injury.J Immunol. 2014 Sep 1;193(5):2469-82. doi: 10.4049/jimmunol.1303370. Epub 2014 Jul 25. J Immunol. 2014. PMID: 25063875 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources