ADAMs 10 and 17 Represent Differentially Regulated Components of a General Shedding Machinery for Membrane Proteins Such as Transforming Growth Factor α, L-Selectin, and Tumor Necrosis Factor α

Author:

Le Gall Sylvain M.1,Bobé Pierre23,Reiss Karina4,Horiuchi Keisuke5,Niu Xiao-Da6,Lundell Daniel6,Gibb David R.7,Conrad Daniel7,Saftig Paul4,Blobel Carl P.18

Affiliation:

1. *Arthritis and Tissue Degeneration Program, Hospital for Special Surgery, New York, NY 10021;

2. Centre National de la Recherche Scientifique, Formation de Recherche en Evolution 2937, Laboratoire d'Oncologie virale, 94801 Villejuif, France;

3. Université Paris-Sud XI, 91405 Orsay, France;

4. Biochemical Institute, Christian-Albrechts-University, 24098 Kiel, Germany;

5. Department of Anti-aging Orthopedic Research and Orthopedic Surgery, Keio University School of Medicine, Tokyo 160-8582, Japan;

6. Department of Inflammation, Schering Plough Research Institute, Kenilworth, NJ 07033-0539;

7. Department of Microbiology and Immunology, Virginia Commonwealth University, Richmond, VA 23298; and

8. Departments of Medicine, and of Physiology and Biophysics, Weill Medical College of Cornell University, New York, NY 10021

Abstract

Protein ectodomain shedding is a critical regulator of many membrane proteins, including epidermal growth factor receptor-ligands and tumor necrosis factor (TNF)-α, providing a strong incentive to define the responsible sheddases. Previous studies identified ADAM17 as principal sheddase for transforming growth factor (TGF)-α and heparin-binding epidermal growth factor, but Ca++influx activated an additional sheddase for these epidermal growth factor receptor ligands in Adam17−/− cells. Here, we show that Ca++influx and stimulation of the P2X7R signaling pathway activate ADAM10 as sheddase of many ADAM17 substrates in Adam17−/− fibroblasts and primary B cells. Importantly, although ADAM10 can shed all substrates of ADAM17 tested here in Adam17−/− cells, acute treatment of wild-type cells with a highly selective ADAM17 inhibitor (SP26) showed that ADAM17 is nevertheless the principal sheddase when both ADAMs 10 and 17 are present. However, chronic treatment of wild-type cells with SP26 promoted processing of ADAM17 substrates by ADAM10, thus generating conditions such as in Adam17−/− cells. These results have general implications for understanding the substrate selectivity of two major cellular sheddases, ADAMs 10 and 17.

Publisher

American Society for Cell Biology (ASCB)

Subject

Cell Biology,Molecular Biology

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