Modification of hippocampal circuitry by adult neurogenesis

被引:100
作者
Song, Juan [1 ,2 ]
Christian, Kimberly M. [1 ,2 ]
Ming, Guo-li [1 ,2 ,3 ]
Song, Hongjun [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Inst Cell Engn, Baltimore, MD 21218 USA
[2] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, Solomon Snyder Dept Neurosci, Baltimore, MD USA
关键词
adult neurogenesis; hippocampus; neural stem cell; activity; NEURAL STEM-CELLS; NEWLY GENERATED NEURONS; LONG-TERM POTENTIATION; ENHANCED SYNAPTIC PLASTICITY; DENTATE GYRUS; GRANULE CELLS; PROLIFERATING CELLS; PROGENITOR CELLS; MAMMALIAN BRAIN; CRITICAL PERIOD;
D O I
10.1002/dneu.22014
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The adult hippocampus is one of the primary neural structures involved in memory formation. In addition to synapse-specific modifications thought to encode information at the subcellular level, changes in the intrahippocampal neuro-populational activity and dynamics at the circuit-level may contribute substantively to the functional capacity of this region. Within the hippocampus, the dentate gyrus has the potential to make a preferential contribution to neural circuit modification owing to the continuous addition of new granule cell population. The integration of newborn neurons into pre-existing circuitry is hypothesized to deliver a unique processing capacity, as opposed to merely replacing dying granule cells. Recent studies have begun to assess the impact of hippocampal neurogenesis by examining the extent to which adult-born neurons participate in hippocampal networks, including when newborn neurons become engaged in ongoing network activity and how they modulate circuit dynamics via their unique intrinsic physiological properties. Understanding the contributions of adult neurogenesis to hippocampal function will provide new insight into the fundamental aspects of brain plasticity, which can be used to guide therapeutic interventions to replaceneural populations damaged by disease or injury. (C) 2012 Wiley Periodicals, Inc. Develop Neurobiol 72: 10321043, 2012
引用
收藏
页码:1032 / 1043
页数:12
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