Perisomatic-Targeting Granule Cells in the Mouse Olfactory Bulb

被引:25
|
作者
Naritsuka, Hiromi
Sakai, Kazuhisa [2 ]
Hashikawa, Tsutomu [2 ]
Mori, Kensaku
Yamaguchi, Masahiro [1 ]
机构
[1] Univ Tokyo, Dept Physiol, Grad Sch Med, Bunkyo Ku, Tokyo 1130033, Japan
[2] RIKEN, Brain Sci Inst, Lab Neural Architecture, Wako, Saitama 3510198, Japan
基金
日本学术振兴会;
关键词
interneuron subtype; subcellular targeting; reciprocal synapse; ADULT NEUROGENESIS; NERVOUS-SYSTEM; IN-VIVO; IMMUNOREACTIVE NEURONS; GABAERGIC INTERNEURONS; MITRAL/TUFTED CELLS; RECIPROCAL SYNAPSES; SYNAPTIC INHIBITION; SUBVENTRICULAR ZONE; DENDRITIC SPINES;
D O I
10.1002/cne.22063
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Inhibitory interneurons in the hippocampus and neocortex are differentiated into several morphological and functional subtypes that innervate distinct subcellular domains of principal neurons. In the olfactory bulb (OB), odor information is processed by local neuronal circuits that include the major inhibitory interneuron, granule cells (GCs). All GCs reported to date target their inhibitory output synapses mainly to dendrites of mitral cells (MCs) and tufted cells (TCs) in the external plexiform layer (EPL). Here we identified a novel type of GC that targets output synapses selectively to the perisomatic region of MCs. In the OB of adult transgenic mice expressing green fluorescent protein (GFP) under the control of nestin gene regulatory regions, we observed cells in the granule cell layer (GCL) that have GC-like morphology and strongly express GFP (referred to as type S cells). Type S cells expressed NeuN and GAD67, molecular markers for GCs. Intracellular labeling of type S cells revealed that their dendrites did not enter the EPL, but formed branches and spines within the GCL, internal plexiform layer, and mitral cell layer. Type S cells typically had huge spines at the ends of the apical dendrites. Some of the terminal spines attached to the perisomatic region of MCs and formed dendrosomatic reciprocal synapses with a presumed granule-to-mitral inhibitory synapse and a mitral-to-granule excitatory synapse. These findings indicate the morphological differentiation of GCs into dendritic-targeting and perisomatic-targeting subsets, and suggest the functional differentiation of the GC subsets in the processing of odor information in the OB. J. Comp. Neurol. 515:409-426, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:409 / 426
页数:18
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