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Volume 396, Issue 1 p. 21-25
Research letter
Free Access

Induction of γ-glutamylcysteine synthetase by cigarette smoke is associated with AP-1 in human alveolar epithelial cells

Irfan Rahman

Irfan Rahman

Respiratory Medicine Unit, Department of Medicine, Rayne Laboratory, Lauriston Place, Edinburgh EH3 9YW, UK

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Christopher A.D. Smith

Christopher A.D. Smith

Department of Pathology, Rayne Laboratory, University of Edinburgh, Edinburgh, UK

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Mark F. Lawson

Mark F. Lawson

Respiratory Medicine Unit, Department of Medicine, Rayne Laboratory, Lauriston Place, Edinburgh EH3 9YW, UK

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David J. Harrison

David J. Harrison

Department of Pathology, Rayne Laboratory, University of Edinburgh, Edinburgh, UK

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William MacNee

William MacNee

Respiratory Medicine Unit, Department of Medicine, Rayne Laboratory, Lauriston Place, Edinburgh EH3 9YW, UK

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First published: October 28, 1996
Citations: 131
Corresponding author. Fax: (44) (131) 536 3255.

Abstract

Increased levels of glutathione (GSH) occur in the epithelial lining fluid (ELF) of chronic cigarette smokers. Therefore we investigated the effect of cigarette smoke condensate solution (CSC) on GSH synthesis and the regulation of γ-glutamylcysteine synthetase (γGCS) in human type II alveolar epithelial cells (A549). CSC exposure increased GSH levels, γGCS activity and γGCS heavy subunit (HS) mRNA, as well as increasing DNA binding of the activator protein-1 (AP-1) and the human antioxidant response element (hARE). Transfection of deletion constructs of the γGCS-HS promoter in a chloramphenicol acetyl transferase (CAT) reporter system revealed that an hARE, present within promoter, is not required for the CSC mediated induction. We conclude that CSC induction of γGCS-HS expression is associated with AP-1/AP-1-like responsive elements.