Table of Contents

Synaptic Autoregulation by Metalloproteases and γ-Secretase

  1. Edward B. Ziff1
  1. 1Departments of Biochemistry and
  2. 2 Psychiatry, New York University Langone Medical Center, New York, New York 10016,
  3. 3Nathan Kline Institute for Psychiatric Research, Orangeburg, New York, 10962,
  4. 4Department of Molecular and Medical Pharmacology, University of California, Los Angeles, California 90095, and
  5. 5Department of Cell and Developmental Biology, Neuroscience Center, University of North Carolina, Chapel Hill, North Carolina 27599
  1. Author contributions: S.R. and E.B.Z. designed research; S.R., L.K., I.N., and R.J.W. performed research; P.M.M. and X.L. contributed unpublished reagents/analytic tools; S.R., I.N., and R.J.W. analyzed data; S.R., I.N., R.J.W., and E.B.Z. wrote the paper.

Abstract

The proteolytic machinery comprising metalloproteases and γ-secretase, an intramembrane aspartyl protease involved in Alzheimer's disease, cleaves several substrates in addition to the extensively studied amyloid precursor protein. Some of these substrates, such as N-cadherin, are synaptic proteins involved in synapse remodeling and maintenance. Here we show, in rats and mice, that metalloproteases and γ-secretase are physiologic regulators of synapses. Both proteases are synaptic, with γ-secretase tethered at the synapse by δ-catenin, a synaptic scaffolding protein that also binds to N-cadherin and, through scaffolds, to AMPA receptor and a metalloprotease. Activity-dependent proteolysis by metalloproteases and γ-secretase takes place at both sides of the synapse, with the metalloprotease cleavage being NMDA receptor-dependent. This proteolysis decreases levels of synaptic proteins and diminishes synaptic transmission. Our results suggest that activity-dependent substrate cleavage by synaptic metalloproteases and γ-secretase modifies synaptic transmission, providing a novel form of synaptic autoregulation.

  • Received May 19, 2011.
  • Revision received June 22, 2011.
  • Accepted June 24, 2011.