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Am J Respir Cell Mol Biol ; 51(4): 568-74, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-24816162

RESUMO

Diacetyl (DA), a component of artificial butter flavoring, has been linked to the development of bronchiolitis obliterans (BO), a disease of airway epithelial injury and airway fibrosis. The epidermal growth factor receptor ligand, amphiregulin (AREG), has been implicated in other types of epithelial injury and lung fibrosis. We investigated the effects of DA directly on the pulmonary epithelium, and we hypothesized that DA exposure would result in epithelial cell shedding of AREG. Consistent with this hypothesis, we demonstrate that DA increases AREG by the pulmonary epithelial cell line NCI-H292 and by multiple independent primary human airway epithelial donors grown under physiologically relevant conditions at the air-liquid interface. Furthermore, we demonstrate that AREG shedding occurs through a TNF-α-converting enzyme (TACE)-dependent mechanism via inhibition of TACE activity in epithelial cells using the small molecule inhibitor, TNF-α protease inhibitor-1, as well as TACE-specific small inhibitor RNA. Finally, we demonstrate supportive in vivo results showing increased AREG transcript and protein levels in the lungs of rodents with DA-induced BO. In summary, our novel in vitro and in vivo observations suggest that further study of AREG is warranted in the pathogenesis of DA-induced BO.


Assuntos
Bronquiolite Obliterante/induzido quimicamente , Diacetil/toxicidade , Família de Proteínas EGF/metabolismo , Células Epiteliais/efeitos dos fármacos , Aromatizantes/toxicidade , Mucosa Respiratória/efeitos dos fármacos , Proteínas ADAM/antagonistas & inibidores , Proteínas ADAM/genética , Proteínas ADAM/metabolismo , Proteína ADAM17 , Anfirregulina , Bronquiolite Obliterante/genética , Bronquiolite Obliterante/metabolismo , Linhagem Celular , Relação Dose-Resposta a Droga , Família de Proteínas EGF/genética , Inibidores Enzimáticos/farmacologia , Células Epiteliais/metabolismo , Células Epiteliais/patologia , Humanos , Fibrose Pulmonar/induzido quimicamente , Fibrose Pulmonar/metabolismo , Fibrose Pulmonar/patologia , Interferência de RNA , Mucosa Respiratória/metabolismo , Mucosa Respiratória/patologia , Fatores de Tempo , Transfecção , Regulação para Cima
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