1. Inducible expression and regulation of the alpha 1-acid glycoprotein gene by alveolar macrophages: prostaglandin E2 and cyclic AMP act as new positive stimuli.
- Author
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Fournier T, Bouach N, Delafosse C, Crestani B, and Aubier M
- Subjects
- Adult, Animals, Bucladesine pharmacology, Cells, Cultured, Female, Gene Expression Regulation drug effects, Humans, Inflammation immunology, Inflammation metabolism, Lung immunology, Lung metabolism, Lung pathology, Macrophages, Alveolar drug effects, Macrophages, Alveolar immunology, Macrophages, Peritoneal metabolism, Male, Middle Aged, Monocytes metabolism, Orosomucoid metabolism, Protein Biosynthesis, RNA biosynthesis, RNA, Messenger biosynthesis, RNA, Messenger metabolism, Rats, Rats, Sprague-Dawley, Cyclic AMP physiology, Dinoprostone physiology, Gene Expression Regulation immunology, Macrophages, Alveolar metabolism, Orosomucoid biosynthesis, Orosomucoid genetics
- Abstract
We have reported that alpha 1-acid glycoprotein (AGP) gene expression was induced in lung tissue and in alveolar type II cells during pulmonary inflammatory processes, suggesting that local production of this immunomodulatory protein might contribute to the modulation of inflammation within the alveolar space. Because AGP may also be secreted by other cell types in the alveolus, we have investigated the expression and the regulation of the AGP gene in human and rat alveolar macrophages. Spontaneous AGP secretion by alveolar macrophages was increased 4-fold in patients with interstitial lung involvement compared with that in controls. In the rat, immunoprecipitation of [35S]methionine-labeled cell lysates showed that alveolar macrophages synthesize and secrete AGP. IL-1 beta had no effect by itself, but potentiated the dexamethasone-induced increase in AGP production. RNase protection assay demonstrated that AGP mRNA, undetectable in unstimulated cells, was induced by dexamethasone. Conditioned medium from LPS-stimulated macrophages as well as IL-1 beta had no effect by themselves, but potentiated the dexamethasone-induced increase in AGP mRNA levels. In addition to cytokines, PGE2 as well as dibutyryl cAMP increased AGP mRNA levels in the presence of dexamethasone. When AGP expression in other cells of the monocyte/macrophage lineage was examined, weak and no AGP production by human blood monocytes and by rat peritoneal macrophages, respectively, were observed. Our data showed that 1) AGP expression is inducible specifically in alveolar macrophages in vivo and in vitro; and 2) PGE2 and cAMP act as new positive stimuli for AGP gene expression.
- Published
- 1999