Circuit-specific and neuronal subcellular-wide E-I balance in cortical pyramidal cells

被引:11
|
作者
Yang, Weiguo [1 ]
Sun, Qian-Quan [1 ]
机构
[1] Univ Wyoming, Dept Zool & Physiol, Laramie, WY 82071 USA
来源
SCIENTIFIC REPORTS | 2018年 / 8卷
关键词
BARREL CORTEX; SYNAPTIC INPUT; INHIBITION; EXCITATION; CONNECTIVITY; LAYER; INTERNEURONS; ORGANIZATION; SELECTIVITY; NETWORKS;
D O I
10.1038/s41598-018-22314-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We used ChR2-assisted circuit mapping (CRACM) to examine neuronal/compartmental excitatory and inhibitory synaptic balance (E-I balance) in pyramidal cells (PCs) located in several brain regions (including both neocortices and paleocortices). Within the vS1, different inputs on the same neurons, or the same inputs formed on different targets, induced different E/I ratios. E/I ratios in PCs from different regions were largely different. Chemogenetic silencing of somatostatin (SOM)- or parvalbumin (PV)-containing interneurons (INs) while optogenetically activating long-range M1 inputs demonstrated differential contribution of PV and SOM INs to the E/I ratios in a layer-specific manner in S1. Our results thus demonstrate that there are both universal subcellular-wide E-I balance within single PC and high specificity in the value of E/I ratios across different circuits (i.e. visual, somatosensory, piriform and hippocampal). Specificity of E/I balance are likely caused by unique glutamatergic innervation of interneurons. The dichotomy of high specificity and generalization of subcellular E-I balance in different circuits forms the basis for further understanding of neuronal computation under physiological conditions and various neuro-psychiatric disease-states.
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页数:15
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