Critical role of the disintegrin metalloprotease ADAM17 for intestinal inflammation and regeneration in mice

Author:

Chalaris Athena1,Adam Nina1,Sina Christian1,Rosenstiel Philip1,Lehmann-Koch Judith2,Schirmacher Peter2,Hartmann Dieter3,Cichy Joanna4,Gavrilova Olga1,Schreiber Stefan1,Jostock Thomas1,Matthews Vance1,Häsler Robert1,Becker Christoph5,Neurath Markus F.5,Reiß Karina11,Saftig Paul1,Scheller Jürgen1,Rose-John Stefan1

Affiliation:

1. Institute of Biochemistry, Institute of Clinical Molecular Biology, and Clinical Research Unit, Department of Dermatology, Christian-Albrechts-University Kiel, D-24098 Kiel, Germany

2. Department of Pathology, University of Heidelberg, D-69123 Heidelberg, Germany

3. Institute of Anatomy, University of Bonn, D-53115 Bonn, Germany

4. Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, 30-387 Kraków, Poland

5. Internal Medicine, University of Erlangen, D-91054 Erlangen, Germany

Abstract

The protease a disintegrin and metalloprotease (ADAM) 17 cleaves tumor necrosis factor (TNF), L-selectin, and epidermal growth factor receptor (EGF-R) ligands from the plasma membrane. ADAM17 is expressed in most tissues and is up-regulated during inflammation and cancer. ADAM17-deficient mice are not viable. Conditional ADAM17 knockout models demonstrated proinflammatory activities of ADAM17 in septic shock via shedding of TNF. We used a novel gene targeting strategy to generate mice with dramatically reduced ADAM17 levels in all tissues. The resulting mice called ADAM17ex/ex were viable, showed compromised shedding of ADAM17 substrates from the cell surface, and developed eye, heart, and skin defects as a consequence of impaired EGF-R signaling caused by failure of shedding of EGF-R ligands. Unexpectedly, although the intestine of unchallenged homozygous ADAM17ex/ex mice was normal, ADAM17ex/ex mice showed substantially increased susceptibility to inflammation in dextran sulfate sodium colitis. This was a result of impaired shedding of EGF-R ligands resulting in failure to phosphorylate STAT3 via the EGF-R and, consequently, in defective regeneration of epithelial cells and breakdown of the intestinal barrier. Besides regulating the systemic availability of the proinflammatory cytokine TNF, our results demonstrate that ADAM17 is needed for vital regenerative activities during the immune response. Thus, our mouse model will help investigate ADAM17 as a potential drug target.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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