Abstract

SORCS3 is an orphan receptor of the VPS10P domain receptor family, a group of sorting and signaling receptors central to many pathways in control of neuronal viability and function. SORCS3 is highly expressed in the CA1 region of the hippocampus, but the relevance of this receptor for hippocampal activity remained absolutely unclear. Here, we show that SORCS3 localizes to the postsynaptic density and that loss of receptor activity in gene-targeted mice abrogates NMDA receptor-dependent and -independent forms of long-term depression (LTD). Consistent with a loss of synaptic retraction, SORCS3-deficient mice suffer from deficits in behavioral activities associated with hippocampal LTD, particularly from an accelerated extinction of fear memory. A possible molecular mechanism for SORCS3 in synaptic depression was suggested by targeted proteomics approaches that identified the ability of SORCS3 to functionally interact with PICK1, an adaptor that sorts glutamate receptors at the postsynapse. Faulty localization of PICK1 in SORCS3-deficient neurons argues for altered glutamate receptor trafficking as the cause of altered synaptic plasticity in the SORCS3-deficient mouse model. In conclusion, our studies have identified a novel function for VPS10P domain receptors in control of synaptic depression and suggest SORCS3 as a novel factor modulating aversive memory extinction.

Highlights

  • VPS10P domain receptors are a unique class of sorting and signaling receptors expressed in the nervous system

  • SORCS3 is expressed in the postsynaptic density of hippocampal neurons

  • VPS10P domain receptors emerge as central regulators of neuronal viability and function

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Summary

Introduction

VPS10P domain receptors are a unique class of sorting and signaling receptors expressed in the nervous system. Five receptors form this gene family in mammals designated sortilin [1], sorting-related receptor with A-type repeats (SORLA) [2,3] as well as SORCS1, SORCS2, and SORCS3 [4]. All family members are characterized by a 700 amino acid module in their extracellular domain, initially identified in the yeast sorting receptor VPS10P (vacuolar protein sorting 10 protein) [5]. Three VPS10P domain receptors have been studied in detail documenting the central role played by this gene family in control of neuronal viability and function (reviewed in 6). SORLA and SORCS1 act as neuronal receptors for the amyloid precursor protein (APP) controlling proteolytic breakdown of this precursor into neurotoxic amyloid-β peptides, a pathological mechanism in Alzheimer’s disease [11,12,13,14,15]

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