Abstract

An important feature of long-term synaptic plasticity is the prolonged maintenance of plastic changes in synaptic transmission. The trafficking of AMPA-type glutamate receptors (AMPARs) is involved in the expression of many forms of synaptic plasticity, yet the subsequent events accomplishing the maintenance of plastic changes in synaptic AMPAR numbers are not fully understood. Here, we find that maintenance of cerebellar long-term depression results from a reduction in the number of AMPARs residing within endocytic recycling pathways. We then develop a genetically encoded, photosensitive inhibitor of late endosome sorting and use this to discover that initial maintenance of long-term depression relies on timely regulated late endosome sorting, which exhibits a threshold as well as switch-like behavior. Thus, our results indicate that recycling AMPAR numbers are reduced by a switching machinery of transient late endosome sorting, and that this process enables the transition from basal synaptic transmission to long-term depression maintenance.

Highlights

  • An important feature of long-term synaptic plasticity is the prolonged maintenance of plastic changes in synaptic transmission

  • TeTx causes a reduction of parallel fiber (PF)-EPSCs15, which results from the reduction in synaptic amino-3hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-type glutamate receptors (AMPARs) numbers by TeTx interrupting AMPAR reinsertion into the plasma membrane

  • The time constant of the reduction in PF-excitatory postsynaptic currents (EPSCs) amplitude represents the speed of constitutive AMPAR internalization, while the degree of reduction is proportional to the number of AMPARs within the recycling loop

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Summary

Introduction

An important feature of long-term synaptic plasticity is the prolonged maintenance of plastic changes in synaptic transmission. Our results indicate that recycling AMPAR numbers are reduced by a switching machinery of transient late endosome sorting, and that this process enables the transition from basal synaptic transmission to long-term depression maintenance. Application of a PKC inhibitor 20 min after LTD induction can result in two distinct responses: either sustained depression, leading to LTD, or transient depression, which allows synaptic transmission to recover to basal levels[11] These results indicate that LTD consists of at least two components distinguished by the responses to the timed application of PKC inhibitor, a reversible expression phase and an irreversible maintenance phase. The properties and timing of LE sorting during LTD are completely unknown

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