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Review
. 2013 Dec 2;369(1633):20130288.
doi: 10.1098/rstb.2013.0288. Print 2014 Jan 5.

The synaptic plasticity and memory hypothesis: encoding, storage and persistence

Tomonori Takeuchi  1 , Adrian J Duszkiewicz, Richard G M Morris
Affiliations
Review

The synaptic plasticity and memory hypothesis: encoding, storage and persistence

Tomonori Takeuchi et al. Philos Trans R Soc Lond B Biol Sci. .

Abstract

The synaptic plasticity and memory hypothesis asserts that activity-dependent synaptic plasticity is induced at appropriate synapses during memory formation and is both necessary and sufficient for the encoding and trace storage of the type of memory mediated by the brain area in which it is observed. Criteria for establishing the necessity and sufficiency of such plasticity in mediating trace storage have been identified and are here reviewed in relation to new work using some of the diverse techniques of contemporary neuroscience. Evidence derived using optical imaging, molecular-genetic and optogenetic techniques in conjunction with appropriate behavioural analyses continues to offer support for the idea that changing the strength of connections between neurons is one of the major mechanisms by which engrams are stored in the brain.

Keywords: dopamine; engram; initial consolidation; long-term potentiation; memory; synaptic plasticity.

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Figures

Figure 1.
Figure 1.
Illustrative findings relevant to the established criteria for assessing the SPM hypothesis. (a,b) Detectability. Field-potentials are increased on some but not all electrodes of a multi-electrode array in area CA1 following inhibitory avoidance learning (Adapted with permission from Whitlock et al. [42] © AAAS) (a). AMPA receptor trafficking detected optically using a GFP label in association with learning, with GluA1 targeted specifically at mature, mushroom-shaped spines (Adapted with permission from Matsuo et al. [43] © AAAS) (b). (c–e) Anterograde alterations. Pharmacological blockade of NMDA receptors in rats with chronic infusion of D-AP5 impairs spatial learning (Adapted with permission from Morris et al. [44]) (c). Genetic knock-out of GluN2A in mice also impairs spatial learning in the watermaze (Adapted with permission from Sakimura et al. [45] © Macmillan Publishers Ltd) (d). CA1 pyramidal cell-specific knockout of GluN1 in mice also impairs selective searching in the watermaze (Adapted with permission from Tsien et al. [46,47] © Elsevier) (e). (f,g) Retrograde alterations. Successful abolition by ZIP of long-lasting LTP 22 h after its initial induction (f). Corresponding abolition of long-term place-memory on a rotating platform by ZIP (Adapted with permission from Pastalkova et al. [48] © AAAS) (g).
Figure 2.
Figure 2.
Hypothetical experiment testing the prediction that LTP at a given set of synapses is sufficient for engram formation. (a) Activity-dependent expression of hypothetical Ca2+ channel in hippocampal CA1 area. The IEG promoter-driven tTA transgenic animal is injected with a viral vector in which the hypothetical light- or exogenous ligand-activated Ca2+ channel with tagged synapse-targeting sequence is expressed in an activity-dependent and Dox-regulated manner. (b) Memory encoding in CA1. A specific pattern of activation of afferent fibres results in Hebbian LTP at a fraction of synapses onto CA1 pyramidal cells. (c) Synaptic tagging and capture. In absence of Dox, strong encoding results in formation of synaptic tags and synthesis of not only PRPs but also the hypothetical Ca2+ channel. The channel protein is then distributed around the neuron and captured by the tagged synapses. (d) Trace decay. The animal is put back on Dox. Synaptic potentiation at hypothetical Ca2+ channel-targeted synapses decays with time. (e) LTP reinstatement. Activation of the Ca2+ channel (either by illumination of the target area or infusion of the exogenous ligand) should result in LTP at synapses tagged during the critical encoding session. A successful mimicry experiment would involve a subsequent demonstration of retrieval of the reinstated memory trace. Sch, Schaffer collaterals; PP, perforant path.
Figure 3.
Figure 3.
One-shot spatial memory task on the event arena for mice. (a) Event arena for one-shot spatial memory task. The event arena during a daily choice phase. Five sand wells are open but only one contains the reward pellets. All open sand wells contain several pellets that are inaccessible to the mouse in order to control for olfactory artefacts. (b) Daily spatial memory performance (errors). Every day mice have two trials to encode the new sand well location, followed by a choice phase. They quickly reach a stable performance level of less than one error (with two errors being the chance level). (c) Novelty-induced enhancement of memory persistence. Critical sessions involve one sample trial followed by an unrewarded probe test 24 h later. 5 min exploration of a novel environment 30 min after encoding results in enhanced persistence of one-shot spatial memory, as demonstrated by increased dig time in the correct location. (d) Prediction of memory enhancement by optogenetic stimulation of catecholaminergic nuclei. We predict that photoactivation of DA cells of the VTA or DA-releasing NA cells of LC in TH-Cre mice injected with Cre-dependent ChR2 virus (AAV-Flex-ChR2) after weak memory encoding will result in enhancement of memory persistence that mimics the novelty effect. Error bars, ±s.e.m; dotted lines, chance level.
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