ADAM10 in Synaptic Physiology and PathologyMusardo S. · Marcello E. · Gardoni F. · Di Luca M.
Department of Pharmacological and Biomolecular Sciences, Università degli Studi di Milano, Milan, Italy
Background: Generation of amyloid-β peptide is at the beginning of a cascade that leads to Alzheimer's disease. Amyloid precursor protein (APP) as well as β- and γ-secretases are the principal players involved in amyloid-β (Aβ) production, while α-secretase cleavage on APP prevents Aβ deposition. A disintegrin and metalloproteinase 10 (ADAM10) has been demonstrated to act as α-secretase in neurons. Objective: Although localization of ADAM10 in the synaptic membrane is the key for its shedding activity, currently, very little is known about the mechanisms that control the synaptic abundance of ADAM10. Results: Two established forms of long-term activity-dependent plasticity, i.e. long-term potentiation and long-term depression (LTD), differentially regulate the synaptic availability and activity of ADAM10. Long-term potentiation decreases ADAM10 surface levels and activity by promoting its endocytosis. This process is mediated by activity-regulated association of ADAM10 with the clathrin adaptor protein 2 (AP2) complex. Conversely, LTD fosters ADAM10 insertion in the membrane and stimulates its activity. Furthermore, ADAM10 interaction with synapse-associated protein 97 (SAP97) is necessary for LTD-induced ADAM10 trafficking and required for LTD maintenance and LTD-induced spine morphology changes. Conclusions: Regulated interaction of ADAM10 with SAP97 and AP2 discloses a novel physiological mechanism of ADAM10 activity regulation at the synapses. This phenomenon produces a situation whereby synaptically regulated ADAM10 activity is positioned to modulate synaptic functioning.
Monica Di Luca
Università degli Studi di Milano
Dipartimento di Scienze Farmacologiche e Biomolecolari, Via Balzaretti, 9
IT-20133 Milan (Italy)
Received: May 20, 2013
Accepted after revision: July 9, 2013
Published online: September 4, 2013
Number of Print Pages : 3
Number of Figures : 0, Number of Tables : 0, Number of References : 14
Vol. 13, No. 2-3, Year 2014 (Cover Date: January 2014)
Journal Editor: Nitsch R.M. (Zürich), Hock C. (Zürich), Rajendran L. (Zürich)
ISSN: 1660-2854 (Print), eISSN: 1660-2862 (Online)
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