Bos Hannah, Miehl Christoph, Oswald Anne-Marie Michelle, Doiron Brent
Department of Mathematics, University of Pittsburgh, Pittsburgh, United States.
Department of Neurobiology, University of Chicago, Chicago, United States.
Elife. 2025 Apr 30;13:RP99808. doi: 10.7554/eLife.99808.
Synaptic inhibition is the mechanistic backbone of a suite of cortical functions, not the least of which are maintaining network stability and modulating neuronal gain. In cortical models with a single inhibitory neuron class, network stabilization and gain control work in opposition to one another - meaning high gain coincides with low stability and vice versa. It is now clear that cortical inhibition is diverse, with molecularly distinguished cell classes having distinct positions within the cortical circuit. We analyze circuit models with pyramidal neurons (E) as well as parvalbumin (PV) and somatostatin (SOM) expressing interneurons. We show how, in E - PV - SOM recurrently connected networks, SOM-mediated modulation can lead to simultaneous increases in neuronal gain and network stability. Our work exposes how the impact of a modulation mediated by SOM neurons depends critically on circuit connectivity and the network state.
突触抑制是一系列皮层功能的机制核心,其中包括维持网络稳定性和调节神经元增益。在具有单一抑制性神经元类别的皮层模型中,网络稳定和增益控制相互对立——也就是说,高增益与低稳定性同时出现,反之亦然。现在很清楚,皮层抑制是多样的,分子特征不同的细胞类别在皮层回路中具有不同的位置。我们分析了包含锥体神经元(E)以及表达小白蛋白(PV)和生长抑素(SOM)的中间神经元的回路模型。我们展示了在E - PV - SOM循环连接网络中,SOM介导的调制如何导致神经元增益和网络稳定性同时增加。我们的工作揭示了SOM神经元介导的调制影响如何关键地取决于回路连接性和网络状态。