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大鼠后穹窿皮质浅层的锥体神经元表现出迟发放电的特性。

Pyramidal neurons in the superficial layers of rat retrosplenial cortex exhibit a late-spiking firing property.

机构信息

Lab for Cortical Organization and Systematics, RIKEN Brain Science Institute, 2-1 Hirosawa, Wako 351-0198, Japan.

出版信息

Brain Struct Funct. 2013 Jan;218(1):239-54. doi: 10.1007/s00429-012-0398-1. Epub 2012 Mar 1.

DOI:10.1007/s00429-012-0398-1
PMID:22383041
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3535347/
Abstract

The rodent granular retrosplenial cortex (GRS) is reciprocally connected with the hippocampus. It is part of several networks implicated in spatial learning and memory, and is known to contain head-direction cells. There are, however, few specifics concerning the mechanisms and microcircuitry underlying its involvement in spatial and mnemonic functions. In this report, we set out to characterize intrinsic properties of a distinctive population of small pyramidal neurons in layer 2 of rat GRS. These neurons, as well as those in adjoining layer 3, were found to exhibit a late-spiking (LS) firing property. We established by multiple criteria that the LS property is a consequence of delayed rectifier and A-type potassium channels. These were identified as Kv1.1, Kv1.4 and Kv4.3 by Genechip analysis, in situ hybridization, single-cell reverse transcriptase-polymerase chain reaction, and pharmacological blockade. The LS property might facilitate comparison or integration of synaptic inputs during an interval delay, consistent with the proposed role of the GRS in memory-related processes.

摘要

啮齿动物颗粒状后隔核(GRS)与海马体相互连接。它是几个与空间学习和记忆相关的网络的一部分,已知包含头方向细胞。然而,关于其参与空间和记忆功能的机制和微电路的具体信息很少。在本报告中,我们着手描述大鼠 GRS 第 2 层中一种独特的小锥体神经元群体的内在特性。通过多种标准确定,LS 特性是延迟整流和 A 型钾通道的结果。通过基因芯片分析、原位杂交、单细胞逆转录聚合酶链反应和药理学阻断鉴定出这些通道为 Kv1.1、Kv1.4 和 Kv4.3。LS 特性可能有助于在间隔延迟期间比较或整合突触输入,这与 GRS 在与记忆相关的过程中的作用一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/d934f22fd4f4/429_2012_398_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/a401005383ca/429_2012_398_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/d6038dea3bae/429_2012_398_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/765843d2a9ed/429_2012_398_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/7aa02c7ea0cb/429_2012_398_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/514b0b8c12f7/429_2012_398_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/7781e3738d24/429_2012_398_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/a3de527b341c/429_2012_398_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/1140a43663df/429_2012_398_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/4803b0273abf/429_2012_398_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/d934f22fd4f4/429_2012_398_Fig10_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/a401005383ca/429_2012_398_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/d6038dea3bae/429_2012_398_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/765843d2a9ed/429_2012_398_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/7aa02c7ea0cb/429_2012_398_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/514b0b8c12f7/429_2012_398_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/7781e3738d24/429_2012_398_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/a3de527b341c/429_2012_398_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/1140a43663df/429_2012_398_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/4803b0273abf/429_2012_398_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a22/3535347/d934f22fd4f4/429_2012_398_Fig10_HTML.jpg

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