dc.creatorDOLHNIKOFF, Marisa
dc.creatorSILVA, Luiz F. F. da
dc.creatorARAUJO, Bianca B. de
dc.creatorGOMES, Higor A. P.
dc.creatorFERNEZLIAN, Sandra
dc.creatorMULDER, Adri
dc.creatorLINDEMAN, Jan H.
dc.creatorMAUAD, Thais
dc.date.accessioned2012-10-19T17:52:32Z
dc.date.accessioned2018-07-04T15:09:35Z
dc.date.available2012-10-19T17:52:32Z
dc.date.available2018-07-04T15:09:35Z
dc.date.created2012-10-19T17:52:32Z
dc.date.issued2009
dc.identifierJOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, v.123, n.5, p.1090-1097, 2009
dc.identifier0091-6749
dc.identifierhttp://producao.usp.br/handle/BDPI/22637
dc.identifier10.1016/j.jaci.2009.02.032
dc.identifierhttp://dx.doi.org/10.1016/j.jaci.2009.02.032
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1619368
dc.description.abstractBackground: Structural and inflammatory changes in asthma involve both the large and small airways, with involvement of the distal lung being related to disease severity. We have previously shown that changes in the extracellular matrix (ECM) composition of the distal lung are associated with loss of alveolar attachments in patients with fatal asthma. However, major ECM elements, such as collagen I and fibronectin and their regulators, have not been addressed at the distal level. Objective: We sought to evaluate ECM remodeling in the distal lungs of asthmatic patients. Methods: Using immunohistochemistry and image analysis, we determined the content of collagen I and III, fibronectin, and matrix metalloproteinases; (MMPs) 1, 2, and 9 and tissue inhibitors of metalloproteinase (MMPs) 1 and 2 in the large and small airways and lung parenchyma of 24 patients with fatal asthma and compared the results with those of 11 nonasthmatic control subjects. Protein content was defined as the area of positive staining divided by basement membrane or septum length. Results: We observed increased collagen I and decreased collagen III content in the small airways of asthmatic patients compared with that seen in control subjects. Greater fibronectin and MMP-1, MMP-2, and MMP-9 content was observed at the outer area of the small airways in asthmatic patients. NIMP content was also increased in the peribronchiolar parenchyma in asthmatic patients. In contrast, TIMP expression was only increased in the large airways of asthmatic patients compared with that seen in control subjects. Conclusions: The outer area of the small airways is a major site of ECM remodeling in fatal asthma, potentially contributing to functional changes and the loss of airway-parenchyma interdependence observed in patients with fatal asthma. (J Allergy Clin Immunol 2009;123:1090-7.)
dc.languageeng
dc.publisherMOSBY-ELSEVIER
dc.relationJournal of Allergy and Clinical Immunology
dc.rightsCopyright MOSBY-ELSEVIER
dc.rightsrestrictedAccess
dc.subjectCollagen
dc.subjectfatal asthma
dc.subjectextracellular matrix
dc.subjectdistal lung
dc.subjectremodeling
dc.titleThe outer wall of small airways is a major site of remodeling in fatal asthma
dc.typeArtículos de revistas


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