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J Allergy Clin Immunol ; 123(5): 1090-7, 1097.e1, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19361849

RESUMO

BACKGROUND: 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 (TIMPs) 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. MMP 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.


Assuntos
Asma/patologia , Matriz Extracelular/patologia , Pulmão/patologia , Adulto , Asma/imunologia , Asma/metabolismo , Colágeno Tipo I/análise , Colágeno Tipo I/imunologia , Colágeno Tipo III/análise , Colágeno Tipo III/imunologia , Matriz Extracelular/imunologia , Matriz Extracelular/metabolismo , Feminino , Fibronectinas/análise , Fibronectinas/imunologia , Humanos , Pulmão/imunologia , Pulmão/metabolismo , Masculino , Metaloproteinases da Matriz/análise , Metaloproteinases da Matriz/imunologia , Pessoa de Meia-Idade , Inibidores Teciduais de Metaloproteinases/análise , Inibidores Teciduais de Metaloproteinases/imunologia
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