An issue central to the study of behavior is the functional relationship between synaptic structure and the changes in synaptic effectiveness that accompany learning and memory. To address this problem we propose to examine the nature, extent and time course of the morphological events at identified synapses that accompany elementary forms of learning and memory and explore the role such structural alterations may play in initiating and maintaining the changes in synaptic function that underlie these behavioral modifications. Toward this end we plan to use a model system, the gill-withdrawal reflex of the marine mollusc Aplysia californica in which several forms of learning and memory have been studied to advantage on both the cellular and molecular level. We have recently exploited this system to examine the morphological basis of short- and long-term habituation and sensitization. Using horseradish peroxidase (HRP) to label the presynaptic terminals of identified sensory neurons (a critical site of plasticity for both forms of learning for both forms of learning) and complete serial reconstruction to analyze the total number and fine structure of snynaptic contacts, we have found that long-term memory is accompanied by structural alterations on two levels of synaptic organization: 1) changes in he number, size, and vesicle complement of focal regions of membrane specialization (active zones) of the synapse, and 2) a parallel but more dramatic and global trend involving modulation of the total number of synaptic varicosities. In contrast, the morphological correlates of short-term memory in Aplysia are restricted to shifts in vesicle populations associated with sensory neuron active zones. These findings provide the first direct evidence that behavioral modification produces structural changes at the level of identified synapses critically involved in learning and suggest a clear difference in the morphological events that accompany memories of differing durations. To explore these issues in more detail, we now plan to examine both the time course and underlying biochemical events responsible for the morphological changes at sensory neuron synapses that accompany short-and long-term memory. A temporal analysis should allow us to determine which class of structural change is necessary for the maintenance of memory and an analysis of mechanism will aid in establishing a more causal relationship between synaptic architecture and the learning process. Finally, to put these studies into perspective and to begin to examine possible mechanistic relationships with higher forms of learning, we also plan to conduct a morphometric analysis of associative learning. the approaches we have developed and the model system we plan to use provide the required specificity to address these problems directly and should increase our understanding of how the functional architecture of the synapse is related to its plastic capabilities.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH037134-10
Application #
3376061
Study Section
Neurosciences Research Review Committee (BPN)
Project Start
1982-06-01
Project End
1994-05-31
Budget Start
1992-09-01
Budget End
1993-05-31
Support Year
10
Fiscal Year
1992
Total Cost
Indirect Cost
Name
New York State Psychiatric Institute
Department
Type
DUNS #
167204994
City
New York
State
NY
Country
United States
Zip Code
10032
Miniaci, Maria Concetta; Kim, Joung-Hun; Puthanveettil, Sathyanarayanan V et al. (2008) Sustained CPEB-dependent local protein synthesis is required to stabilize synaptic growth for persistence of long-term facilitation in Aplysia. Neuron 59:1024-36
Bailey, Craig H; Kandel, Eric R (2008) Synaptic remodeling, synaptic growth and the storage of long-term memory in Aplysia. Prog Brain Res 169:179-98
Hawkins, Robert D; Kandel, Eric R; Bailey, Craig H (2006) Molecular mechanisms of memory storage in Aplysia. Biol Bull 210:174-91
Barco, Angel; Bailey, Craig H; Kandel, Eric R (2006) Common molecular mechanisms in explicit and implicit memory. J Neurochem 97:1520-33
Udo, Hiroshi; Jin, Iksung; Kim, Joung-Hun et al. (2005) Serotonin-induced regulation of the actin network for learning-related synaptic growth requires Cdc42, N-WASP, and PAK in Aplysia sensory neurons. Neuron 45:887-901
Bailey, Craig H; Kandel, Eric R; Si, Kausik (2004) The persistence of long-term memory: a molecular approach to self-sustaining changes in learning-induced synaptic growth. Neuron 44:49-57
Kim, Joung-Hun; Udo, Hiroshi; Li, Hsiu-Ling et al. (2003) Presynaptic activation of silent synapses and growth of new synapses contribute to intermediate and long-term facilitation in Aplysia. Neuron 40:151-65
Bailey, C H; Giustetto, M; Zhu, H et al. (2000) A novel function for serotonin-mediated short-term facilitation in aplysia: conversion of a transient, cell-wide homosynaptic hebbian plasticity into a persistent, protein synthesis-independent synapse-specific enhancement. Proc Natl Acad Sci U S A 97:11581-6
Bailey, C H (1999) Structural changes and the storage of long-term memory in Aplysia. Can J Physiol Pharmacol 77:738-47
Casadio, A; Martin, K C; Giustetto, M et al. (1999) A transient, neuron-wide form of CREB-mediated long-term facilitation can be stabilized at specific synapses by local protein synthesis. Cell 99:221-37

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