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      The Arc of synaptic memory

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          Abstract

          The immediate early gene Arc is emerging as a versatile, finely tuned system capable of coupling changes in neuronal activity patterns to synaptic plasticity, thereby optimizing information storage in the nervous system. Here, we attempt to overview the Arc system spanning from transcriptional regulation of the Arc gene, to dendritic transport, metabolism, and translation of Arc mRNA, to post-translational modification, localization, and degradation of Arc protein. Within this framework we discuss the function of Arc in regulation of actin cytoskeletal dynamics underlying consolidation of long-term potentiation (LTP) and regulation of AMPA-type glutamate receptor endocytosis underlying long-term depression (LTD) and homeostatic plasticity. Behaviorally, Arc has a key role in consolidation of explicit and implicit forms of memory, with recent work implicating Arc in adaptation to stress as well as maladaptive plasticity connected to drug addiction. Arc holds considerable promise as a “master regulator” of protein synthesis-dependent forms of synaptic plasticity, but the mechanisms that modulate and switch Arc function are only beginning to be elucidated.

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          Most cited references122

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          Mechanisms and functional implications of adult neurogenesis.

          The generation of new neurons is sustained throughout adulthood in the mammalian brain due to the proliferation and differentiation of adult neural stem cells. In this review, we discuss the factors that regulate proliferation and fate determination of adult neural stem cells and describe recent studies concerning the integration of newborn neurons into the existing neural circuitry. We further address the potential significance of adult neurogenesis in memory, depression, and neurodegenerative disorders such as Alzheimer's and Parkinson's disease.
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            Synaptic plasticity: multiple forms, functions, and mechanisms.

            Experiences, whether they be learning in a classroom, a stressful event, or ingestion of a psychoactive substance, impact the brain by modifying the activity and organization of specific neural circuitry. A major mechanism by which the neural activity generated by an experience modifies brain function is via modifications of synaptic transmission; that is, synaptic plasticity. Here, we review current understanding of the mechanisms of the major forms of synaptic plasticity at excitatory synapses in the mammalian brain. We also provide examples of the possible developmental and behavioral functions of synaptic plasticity and how maladaptive synaptic plasticity may contribute to neuropsychiatric disorders.
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              The self-tuning neuron: synaptic scaling of excitatory synapses.

              Homeostatic synaptic scaling is a form of synaptic plasticity that adjusts the strength of all of a neuron's excitatory synapses up or down to stabilize firing. Current evidence suggests that neurons detect changes in their own firing rates through a set of calcium-dependent sensors that then regulate receptor trafficking to increase or decrease the accumulation of glutamate receptors at synaptic sites. Additional mechanisms may allow local or network-wide changes in activity to be sensed through parallel pathways, generating a nested set of homeostatic mechanisms that operate over different temporal and spatial scales.
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                Author and article information

                Contributors
                +47-5-5586032 , +47-5-5586410 , clive.bramham@biomed.uib.no
                Journal
                Exp Brain Res
                Experimental Brain Research. Experimentelle Hirnforschung. Experimentation Cerebrale
                Springer-Verlag (Berlin/Heidelberg )
                0014-4819
                1432-1106
                19 August 2009
                19 August 2009
                January 2010
                : 200
                : 2
                : 125-140
                Affiliations
                Department of Biomedicine and Bergen Mental Health Research Center, University of Bergen, Jonas Lies vei 91, 5009 Bergen, Norway
                Article
                1959
                10.1007/s00221-009-1959-2
                2803749
                19690847
                faac721b-a0c9-424e-99fe-c611668d16a1
                © The Author(s) 2009
                History
                : 11 June 2009
                : 18 July 2009
                Categories
                Review
                Custom metadata
                © Springer-Verlag 2010

                Neurosciences
                neurogenesis,synaptic plasticity,stress,gene expression,rna decay,drug addiction,ltp/ltd,memory
                Neurosciences
                neurogenesis, synaptic plasticity, stress, gene expression, rna decay, drug addiction, ltp/ltd, memory

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