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齿状回海马里层细胞的局部和远程电路连接。

Local and Long-Range Circuit Connections to Hilar Mossy Cells in the Dentate Gyrus.

机构信息

Department of Anatomy and Neurobiology, School of Medicine, University of California, Irvine, CA 92697-1275.

Department of Physiology and Biophysics, School of Medicine, University of California, Irvine, CA 92697-4560.

出版信息

eNeuro. 2017 Apr 19;4(2). doi: 10.1523/ENEURO.0097-17.2017. eCollection 2017 Mar-Apr.

Abstract

Hilar mossy cells are the prominent glutamatergic cell type in the dentate hilus of the dentate gyrus (DG); they have been proposed to have critical roles in the DG network. To better understand how mossy cells contribute to DG function, we have applied new viral genetic and functional circuit mapping approaches to quantitatively map and compare local and long-range circuit connections of mossy cells and dentate granule cells in the mouse. The great majority of inputs to mossy cells consist of two parallel inputs from within the DG: an excitatory input pathway from dentate granule cells and an inhibitory input pathway from local DG inhibitory neurons. Mossy cells also receive a moderate degree of excitatory and inhibitory CA3 input from proximal CA3 subfields. Long range inputs to mossy cells are numerically sparse, and they are only identified readily from the medial septum and the septofimbrial nucleus. In comparison, dentate granule cells receive most of their inputs from the entorhinal cortex. The granule cells receive significant synaptic inputs from the hilus and the medial septum, and they also receive direct inputs from both distal and proximal CA3 subfields, which has been underdescribed in the existing literature. Our slice-based physiological mapping studies further supported the identified circuit connections of mossy cells and granule cells. Together, our data suggest that hilar mossy cells are major local circuit integrators and they exert modulation of the activity of dentate granule cells as well as the CA3 region through "back-projection" pathways.

摘要

海拉尔苔状细胞是齿状回(DG)齿状回中的突出谷氨酸能细胞类型;它们被认为在 DG 网络中具有关键作用。为了更好地了解苔状细胞如何为 DG 功能做出贡献,我们应用了新的病毒遗传和功能回路映射方法,定量映射和比较了小鼠中苔状细胞和齿状颗粒细胞的局部和远程回路连接。苔状细胞的绝大多数输入由 DG 内的两个平行输入组成:来自齿状颗粒细胞的兴奋性输入途径和来自局部 DG 抑制性神经元的抑制性输入途径。苔状细胞还接收来自近端 CA3 亚区的适度程度的兴奋性和抑制性 CA3 输入。苔状细胞的远程输入数量稀疏,只能从内侧隔核和隔核纤维核中轻易识别。相比之下,齿状颗粒细胞接收其大部分输入来自内嗅皮层。颗粒细胞从弓状束和内侧隔核接收大量突触输入,并且它们还接收来自远端和近端 CA3 亚区的直接输入,这在现有文献中描述较少。我们基于切片的生理映射研究进一步支持了苔状细胞和颗粒细胞的已识别回路连接。总之,我们的数据表明,海拉尔苔状细胞是主要的局部回路整合器,它们通过“反向投射”途径对齿状颗粒细胞和 CA3 区的活动进行调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6f19/5396130/2a0f73fe6118/enu0021722910001.jpg

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