Abstract

Electrical synapses couple inhibitory neurons across the brain, underlying a variety of functions that are modifiable by activity. Despite recent advances, many functions and contributions of electrical synapses within neural circuitry remain underappreciated. Among these are the sources and impacts of electrical synapse asymmetry. Using multi-compartmental models of neurons coupled through dendritic electrical synapses, we investigated intrinsic factors that contribute to effective synaptic asymmetry and that result in modulation of spike timing and synchrony between coupled cells. We show that electrical synapse location along a dendrite, input resistance, internal dendritic resistance, or directional conduction of the electrical synapse itself each alter asymmetry as measured by coupling between cell somas. Conversely, we note that asymmetrical gap junction (GJ) conductance can be masked by each of these properties. Furthermore, we show that asymmetry modulates spike timing and latency of coupled cells by up to tens of milliseconds, depending on direction of conduction or dendritic location of the electrical synapse. Coordination of rhythmic activity between two cells also depends on asymmetry. These simulations illustrate that causes of asymmetry are diverse, may not be apparent in somatic measurements of electrical coupling, influence dendritic processing, and produce a variety of outcomes on spiking and synchrony of coupled cells. Our findings highlight aspects of electrical synapses that should always be included in experimental demonstrations of coupling, and when assembling simulated networks containing electrical synapses.

Highlights

  • We added an electrical synapse between matched compartments of two identical thalamic reticular nucleus (TRN) model cells and measured the coupling coefficients resulting from hyperpolarizing current applied to and measured at the somas (Fig. 1C1)

  • Asymmetry of transmission at electrical synapses has been widely noted but its specific sources rarely explored in depth, perhaps due to the experimental difficulties of identifying and localizing specific gap junctions (GJs) in vitro or in vivo

  • We have shown that asymmetry can arise from a variety of intrinsic differences in neuronal properties as well as differences in subcellular localization of the gap junction between somas

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Summary

Introduction

Asymmetry at synapses between mammalian neurons is often more modest. Demonstrations of electrical synapse asymmetry are numerous throughout the mammalian brain, including retina (Veruki and Hartveit, 2002), cortex (Galarreta and Hestrin, 2002), inferior olive (Devor and Yarom, 2002), dorsal cochlear nucleus (Apostolides and Trussell, 2013), mesencephalic trigeminal nucleus (Curti et al, 2012), cerebellar Golgi cells (Szoboszlay et al, 2016) and molecular layer interneurons (Alcami and Marty, 2013; Mann-Metzer and Yarom, 1999), and the thalamic reticular nucleus (TRN) (Haas et al, 2011; Sevetson and Haas, 2015; Zolnik and Connors, 2016). Recent results show that asymmetry can be modified during the activity that results in electrical synapse plasticity (Fricker et al, 2021; Haas et al, 2011), indicating that it is a dynamic property that is under activity-dependent regulation

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