• Pierre-Marie Andrault, Andrea C Schamberger, Thibault Chazeirat, Damien Sizaret, Justine Renault, Claudia A Staab-Weijnitz, Elisabeth Hennen, Agnès Petit-Courty, Mylène Wartenberg, Ahlame Saidi, Thomas Baranek, Serge Guyetant, Yves Courty, Oliver Eickelberg, Gilles Lalmanach, and Fabien Lecaille.
• Université de Tours, Tours, France.
• Am. J. Physiol. Lung Cell Mol. Physiol. 2019 Nov 1; 317 (5): L625-L638.

AbstractCigarette smoking has marked effects on lung tissue, including induction of oxidative stress, inflammatory cell recruitment, and a protease/antiprotease imbalance. These effects contribute to tissue remodeling and destruction resulting in loss of lung function in chronic obstructive pulmonary disease (COPD) patients. Cathepsin S (CatS) is a cysteine protease that is involved in the remodeling/degradation of connective tissue and basement membrane. Aberrant expression or activity of CatS has been implicated in a variety of diseases, including arthritis, cancer, cardiovascular, and lung diseases. However, little is known about the effect of cigarette smoking on both CatS expression and activity, as well as its role in smoking-related lung diseases. Here, we evaluated the expression and activity of human CatS in lung tissues from never-smokers and smokers with or without COPD. Despite the presence of an oxidizing environment, CatS expression and activity were significantly higher in current smokers (both non-COPD and COPD) compared with never-smokers, and correlated positively with smoking history. Moreover, we found that the exposure of primary human bronchial epithelial cells to cigarette smoke extract triggered the activation of P2X7 receptors, which in turns drives CatS upregulation. The present data suggest that excessive CatS expression and activity contribute, beside other proteases, to the deleterious effects of cigarette smoke on pulmonary homeostasis.

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