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TSG-6 Potentiates the Antitissue Kallikrein Activity of Inter–-inhibitor through Bikunin Release

Division of Pulmonary and Critical Care Medicine, University of Miami, Miller School of Medicine, Miami, Florida; MRC Immunochemistry Unit, Department of Biochemistry, University of Oxford, Oxford; Faculty of Life Sciences, University of Manchester, Oxford Road, Manchester, United Kingdom; Department of Medical Biochemistry and Microbiology, Uppsala University, Biomedical Center, Uppsala, Sweden

Correspondence and requests for reprints should be addressed to Rosanna M. Forteza, Division of Pulmonary and Critical Care Medicine (R-47), University of Miami School of Medicine, 1600 NW 10th Ave, RMSB 7072A, Miami, FL 33136. E-mail: rforteza{at}miami.edu; and to Anthony J. Day, MRC Immunochemistry Unit, Dept. of Biochemistry; University of Oxford, South Parks Road, Oxford OX1 3QU, UK. E-mail: anthony.day{at}manchester.ac.uk

TSG-6 (the protein product of TNF-stimulated gene-6), an inflammation-associated protein, forms covalent complexes with heavy chains (HCs) from inter–-inhibitor and pre–-inhibitor and associates noncovalently with their common bikunin chain, potentiating the antiplasmin activity of this serine protease inhibitor. We show that TSG-6 and TSG-6·HC complexes are present in bronchoalveolar lavage fluid from patients with asthma and increase after allergen challenge. Immunodetection demonstrated elevated TSG-6 in the airway tissue and secretions of smokers. Experiments conducted in vitro with purified components revealed that bikunin·HC complexes (byproducts of TSG-6·HC formation) release bikunin. Immunoprecipitation revealed that bikunin accounts for a significant proportion of tissue kallikrein inhibition in bronchoalveolar lavage after allergen challenge but not in baseline conditions, confirming that bikunin in its free state, but not when associated with HCs, is a relevant protease inhibitor in airway secretions. In primary cultures of differentiated human airway epithelial and submucosal gland cells, TSG-6 is induced by TNF- and IL-1, which suggests that these cells are responsible for TSG-6 release in vivo. Bikunin and HC3 (i.e., pre–-inhibitor) were also induced by TNF- in primary cultures. Our results suggest that TSG-6 may play an important protective role in bronchial epithelium by increasing the antiprotease screen on the airway lumen.

Key Words: TSG-6 • II • tissue kallikrein • bikunin • airway

CLINICAL RELEVANCE This original work describes a previously unrecognized antiprotease system operating in human airways. The findings of this study may provide new tools for the prevention or/and treatment of airway diseases.

 

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