Molecular Mechanisms of the Memory Trace

被引:130
作者
Asok, Arun [1 ,2 ]
Leroy, Felix [1 ,2 ]
Rayman, Joseph B. [1 ,2 ]
Kandel, Eric R. [1 ,2 ,3 ,4 ]
机构
[1] Columbia Univ, Coll Phys & Surg, Dept Neurosci, New York, NY 10032 USA
[2] Columbia Univ, Zuckerman Mind Brain Behav Inst, New York, NY 10027 USA
[3] Columbia Univ, Howard Hughes Med Inst, New York, NY 10032 USA
[4] Columbia Univ, Kavli Inst Brain Sci, New York, NY 10032 USA
关键词
LONG-TERM FACILITATION; APLYSIA SENSORY NEURONS; PROTEIN-SYNTHESIS; TRANSCRIPTION FACTOR; DNA METHYLATION; ENGRAM CELLS; POTENTIATION; CONSOLIDATION; STORAGE; PHOSPHORYLATION;
D O I
10.1016/j.tins.2018.10.005
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Over the past half-century, we have gained significant insights into the molecular biology of long-term memory storage at the level of the synapse. In recent years, our understanding of the cellular architecture supporting long-term memory traces has also substantially improved. However, the molecular biology of consolidation at the level of neuronal systems has been relatively neglected. In this opinion article, we first examine our current understanding of the cellular mechanisms of synaptic consolidation. We then outline areas requiring further investigation on how cellular changes contribute to systems consolidation. Finally, we highlight recent findings on the cellular architecture of memory traces in rodents and how the application of new technologies will expand our understanding of systems consolidation at the neural circuit level. In the coming years, this research focus will be critical for understanding the evolution of long-term memories and for enabling the development of novel therapeutics which embrace the dynamic nature of memories.
引用
收藏
页码:14 / 22
页数:9
相关论文
共 112 条
[1]   Synapse-specific representation of the identity of overlapping memory engrams [J].
Abdou, Kareem ;
Shehata, Mohammad ;
Choko, Kiriko ;
Nishizono, Hirofumi ;
Matsuo, Mina ;
Muramatsu, Shin-ichi ;
Inokuchi, Kaoru .
SCIENCE, 2018, 360 (6394) :1227-1231
[2]   Molecular mechanisms of memory acquisition, consolidation and retrieval [J].
Abel, T ;
Lattal, KM .
CURRENT OPINION IN NEUROBIOLOGY, 2001, 11 (02) :180-187
[3]   Transcription Factors in Long-Term Memory and Synaptic Plasticity [J].
Alberini, Cristina M. .
PHYSIOLOGICAL REVIEWS, 2009, 89 (01) :121-145
[4]   Optogenetic Inhibitor of the Transcription Factor CREB [J].
Ali, Ahmed M. ;
Reis, Jakeb M. ;
Xia, Yan ;
Rashid, Asim J. ;
Mercaldo, Valentina ;
Walters, Brandon J. ;
Brechun, Katherine E. ;
Borisenko, Vitali ;
Josselyn, Sheena A. ;
Karanicolas, John ;
Woolley, G. Andrew .
CHEMISTRY & BIOLOGY, 2015, 22 (11) :1531-1539
[5]  
[Anonymous], 1948, CONDITIONED REFLEXES
[6]  
[Anonymous], 1949, ORG BEHAV NEUROPHYSI
[7]   Retrovirus-like Gag Protein Arc1 Binds RNA and Traffics across Synaptic Boutons [J].
Ashley, James ;
Cordy, Benjamin ;
Lucia, Diandra ;
Fradkin, Lee G. ;
Budnik, Vivian ;
Thomson, Travis .
CELL, 2018, 172 (1-2) :262-+
[8]   MORPHOLOGICAL BASIS OF LONG-TERM HABITUATION AND SENSITIZATION IN APLYSIA [J].
BAILEY, CH ;
CHEN, M .
SCIENCE, 1983, 220 (4592) :91-93
[9]   STRUCTURAL PLASTICITY AT IDENTIFIED SYNAPSES DURING LONG-TERM-MEMORY IN APLYSIA [J].
BAILEY, CH ;
CHEN, M .
JOURNAL OF NEUROBIOLOGY, 1989, 20 (05) :356-372
[10]   Mutation in the phosphorylation sites of MAP kinase blocks learning-related internalization of apCAM in Aplysia sensory neurons [J].
Bailey, CH ;
Kaang, BK ;
Chen, M ;
Martin, KC ;
Lim, CS ;
Casadio, A ;
Kandel, ER .
NEURON, 1997, 18 (06) :913-924