TspanC8 tetraspanins regulate ADAM10/Kuzbanian trafficking and promote Notch activation in flies and mammals

Author:

Dornier Emmanuel12,Coumailleau Franck34,Ottavi Jean-François12,Moretti Julien34,Boucheix Claude12,Mauduit Philippe12,Schweisguth François34,Rubinstein Eric12

Affiliation:

1. Institut National de la Santé et de la Recherche Médicale (INSERM), U1004, F-94807 Villejuif, France

2. Université Paris-Sud, Institut André Lwoff, F-94807 Villejuif, France

3. Département de Biologie du Développement, et Unité de Signalisation Moléculaire et Activation Cellulaire, Institut Pasteur, F-75015 Paris, France

4. URA 2578, et URA 2582, Centre national de la recherche scientifique (CNRS), F-75015 Paris, France

Abstract

The metalloprotease ADAM10/Kuzbanian catalyzes the ligand-dependent ectodomain shedding of Notch receptors and activates Notch. Here, we show that the human tetraspanins of the evolutionary conserved TspanC8 subfamily (Tspan5, Tspan10, Tspan14, Tspan15, Tspan17, and Tspan33) directly interact with ADAM10, regulate its exit from the endoplasmic reticulum, and that four of them regulate ADAM10 surface expression levels. In an independent RNAi screen in Drosophila, two TspanC8 genes were identified as Notch regulators. Functional analysis of the three Drosophila TspanC8 genes (Tsp3A, Tsp86D, and Tsp26D) indicated that these genes act redundantly to promote Notch signaling. During oogenesis, TspanC8 genes were up-regulated in border cells and regulated Kuzbanian distribution, Notch activity, and cell migration. Furthermore, the human TspanC8 tetraspanins Tspan5 and Tspan14 positively regulated ligand-induced ADAM10-dependent Notch1 signaling. We conclude that TspanC8 tetraspanins have a conserved function in the regulation of ADAM10 trafficking and activity, thereby positively regulating Notch receptor activation.

Publisher

Rockefeller University Press

Subject

Cell Biology

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