Molecular and cellular mechanisms of memory allocation in neuronetworks

被引:66
作者
Won, Jaejoon [1 ,2 ,3 ]
Silva, Alcino J. [1 ,2 ,3 ]
机构
[1] Univ Calif Los Angeles, Dept Neurobiol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Psychiat & Psychol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Brain Res Inst, Los Angeles, CA 90095 USA
关键词
memory allocation; competition; CAMP-response element binding protein (CREB); activity-regulated cytoskeleton-associated protein (Arc); metaplasticity;
D O I
10.1016/j.nlm.2007.08.017
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Determining how neuronal networks encode memories is a key goal of neuroscience. Although neuronal circuit processes involved in encoding, storing and retrieving memory have attracted a great deal of attention, the processes that allocate individual memories to specific neurons within a network have remained elusive. Recent findings unraveled the first insights into the processes that modulate memory allocation in neuronetworks. They showed that neurons in the lateral amygdala compete to take part in auditory fear conditioned memory traces and that the levels of the transcription factor CREB (CAMP-response element binding protein) can affect the probability of a neuron to be recruited into a given memory representation. CREB-mediated transcriptional regulation involves several signaling pathways, known to mediate nuclear responses to diverse behavioral stimuli, along with coordinated interactions with multiple other transcription activators, coactivators and repressors. Moreover, activation of CREB triggers an autoinhibitory feedback loop, a metaplastic process that could be used to allocate memories away from cells that have been recently involved in memory. Beyond CREB, there may be a host of other processes that dynamically modulate memory allocation in neuronetworks by shaping cooperation and competition among neurons. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:285 / 292
页数:8
相关论文
共 67 条
[1]   Metaplasticity: The plasticity of synaptic plasticity [J].
Abraham, WC ;
Bear, MF .
TRENDS IN NEUROSCIENCES, 1996, 19 (04) :126-130
[2]   Chromatin acetylation, memory, and LTP are impaired in CBP+/- mice:: A model for the cognitive deficit in Rubinstein-Taybi syndrome and its amelioration [J].
Alarcón, JM ;
Malleret, G ;
Touzani, K ;
Vronskaya, S ;
Ishii, S ;
Kandel, ER ;
Barco, A .
NEURON, 2004, 42 (06) :947-959
[3]   USE OF THE WHOLE-CELL PATCH-CLAMP METHOD IN STUDIES ON THE ROLE OF CAMP IN REGULATING THE SPONTANEOUS FIRING OF LOCUS-COERULEUS NEURONS [J].
ALREJA, M ;
AGHAJANIAN, GK .
JOURNAL OF NEUROSCIENCE METHODS, 1995, 59 (01) :67-75
[4]   APLYSIA CREB2 REPRESSES LONG-TERM FACILITATION - RELIEF OF REPRESSION CONVERTS TRANSIENT FACILITATION INTO LONG-TERM FUNCTIONAL AND STRUCTURAL-CHANGE [J].
BARTSCH, D ;
GHIRARDI, M ;
SKEHEL, PA ;
KARL, KA ;
HERDER, SP ;
CHEN, M ;
BAILEY, CH ;
KANDEL, ER .
CELL, 1995, 83 (06) :979-992
[5]   CREB1 encodes a nuclear activator, a repressor, and a cytoplasmic modulator that form a regulatory unit critical for long-term facilitation [J].
Bartsch, D ;
Casadio, A ;
Karl, KA ;
Serodio, P ;
Kandel, ER .
CELL, 1998, 95 (02) :211-223
[6]   INHIBITION OF OCULAR DOMINANCE COLUMN FORMATION BY INFUSION OF NT-4/5 OR BDNF [J].
CABELLI, RJ ;
HOHN, A ;
SHATZ, CJ .
SCIENCE, 1995, 267 (5204) :1662-1666
[7]   Attenuation of a phosphorylation-dependent activator by an HDAC-PP1 complex [J].
Canettieri, G ;
Morantte, I ;
Guzmán, E ;
Asahara, H ;
Herzig, S ;
Anderson, SD ;
Yates, JR ;
Montminy, M .
NATURE STRUCTURAL BIOLOGY, 2003, 10 (03) :175-181
[8]   The many faces of CREB [J].
Carlezon, WA ;
Duman, RS ;
Nestler, EJ .
TRENDS IN NEUROSCIENCES, 2005, 28 (08) :436-445
[9]   Cell-type-specific binding of the transcription factor CREB to the cAMP-response element [J].
Cha-Molstad, H ;
Keller, DM ;
Yochum, GS ;
Impey, S ;
Goodman, RH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (37) :13572-13577
[10]   Characterization of the mouse adenylyl cyclase type VIII gene promoter:: regulation by cAMP and CREB [J].
Chao, JR ;
Ni, YG ;
Bolaños, CA ;
Rahman, Z ;
DiLeone, RJ ;
Nestler, EJ .
EUROPEAN JOURNAL OF NEUROSCIENCE, 2002, 16 (07) :1284-1294