CaMKII is a leading candidate as a molecular memory. In a first aim, we will explore the hypothesis that CaMKII and phosphatase-1 (PP1) in the postsynaptic density (PSD) form a bistable switch. Monte Carlo simulations will be developed. The model will be used to address a fundamental theoretical question: how is the stability of stored information limited by stochastic fluctuations in the reactions of the small group of molecules at synapses? In a parallel set of biochemical experiments, we will directly test whether the CaMKII/PP1 system in isolated PSDs can act as a bistable switch.
In Aim 2 we examine how synaptic strength can be bi-directionally modified by different patterns of synaptic activation. The moderate Ca2+ elevation during the induction of depotentiation reduces CaMKII phosphorylation through a phosphatase cascade that involves calcineurin, I1 and PP1. Since <1% of synapses are activated during induction active synapses are point sinks/sources, producing dendritic gradients of diffusible molecules such as I1. The buildup of such gradients could potentially explain kinetic aspects of induction and heterosynaptic effects. Because the role of gradients has not been previously considered, it will be useful to make a diffusion model to study how different factors affect the spatial/temporal gradient of possible importance in plasticity. In related physiological experiments, we will test the role of I1 in depotentiation.
Aim 3 relates to recent work indicating that LTP produces a stable increase in synapse size. To understand the principles that might underlie such structural stability, we have formed a team with expertise in physical chemistry, structural biology, neuroscience and physics. Simulations will be used to explore the principles that could underlie structural stability. Together these aims address the deepest issues regard the mechanism by which memories are stored in the brain. The insights derived are likely to be of importance in understanding diseases of memory and suggest strategies for therapeutic intervention.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
1R01NS050944-01
Application #
6887584
Study Section
Special Emphasis Panel (ZRG1-MDCN-C (50))
Program Officer
Talley, Edmund M
Project Start
2004-08-01
Project End
2008-04-30
Budget Start
2004-08-01
Budget End
2005-04-30
Support Year
1
Fiscal Year
2004
Total Cost
$314,426
Indirect Cost
Name
Brandeis University
Department
Type
Organized Research Units
DUNS #
616845814
City
Waltham
State
MA
Country
United States
Zip Code
02454
Zhang, Peng; Lisman, John E (2012) Activity-dependent regulation of synaptic strength by PSD-95 in CA1 neurons. J Neurophysiol 107:1058-66
Pi, Hyun Jae; Otmakhov, Nikolai; Lemelin, David et al. (2010) Autonomous CaMKII can promote either long-term potentiation or long-term depression, depending on the state of T305/T306 phosphorylation. J Neurosci 30:8704-9
Pi, Hyun Jae; Otmakhov, Nikolai; El Gaamouch, Farida et al. (2010) CaMKII control of spine size and synaptic strength: role of phosphorylation states and nonenzymatic action. Proc Natl Acad Sci U S A 107:14437-42
Pi, Hyun Jae; Lisman, John E (2008) Coupled phosphatase and kinase switches produce the tristability required for long-term potentiation and long-term depression. J Neurosci 28:13132-8
Mullasseril, Praseeda; Dosemeci, Ayse; Lisman, John E et al. (2007) A structural mechanism for maintaining the 'on-state'of the CaMKII memory switch in the post-synaptic density. J Neurochem 103:357-64
Fusi, Stefano; Asaad, Wael F; Miller, Earl K et al. (2007) A neural circuit model of flexible sensorimotor mapping: learning and forgetting on multiple timescales. Neuron 54:319-33
Lisman, John E; Raghavachari, Sridhar; Tsien, Richard W (2007) The sequence of events that underlie quantal transmission at central glutamatergic synapses. Nat Rev Neurosci 8:597-609
Sanhueza, Magdalena; McIntyre, Charmian C; Lisman, John E (2007) Reversal of synaptic memory by Ca2+/calmodulin-dependent protein kinase II inhibitor. J Neurosci 27:5190-9
Zhabotinsky, Anatol M; Camp, R Nicholas; Epstein, Irving R et al. (2006) Role of the neurogranin concentrated in spines in the induction of long-term potentiation. J Neurosci 26:7337-47
Jensen, Ole; Lisman, John E (2005) Hippocampal sequence-encoding driven by a cortical multi-item working memory buffer. Trends Neurosci 28:67-72

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