microRNA-218-5p Coordinates Scaling of Excitatory and Inhibitory Synapses during Homeostatic Synaptic Plasticity

Abstract

Homeostatic synaptic plasticity (HSP) is a fundamental neuronal mechanism that allows networks to compensate for prolonged changes in activity by adjusting synaptic strength. This process is crucial for maintaining stable brain function and has been implicated in memory consolidation during sleep. While scaling of both excitatory and inhibitory synapses plays an important role during homeostatic synaptic plasticity, molecules coordinating both of these processes are unknown. In this study, we investigate the role of miR-218-5p as a regulator of inhibitory and excitatory synapses in the context of picrotoxin (PTX)-induced homeostatic synaptic downscaling (HSD) in rat hippocampal neurons. Using enrichment analysis of miRNA-binding sites in differentially expressed genes changing upon PTX-induced HSD, we bioinformatically predicted and experimentally validated increased miR-218-5p activity upon PTX-treatment in the process compartment. By monitoring synapse structure in vitro with confocal microscopy, we demonstrate that inhibiting miR-218-5p activity exerts a dual effect during HSD: it prevents the downscaling of excitatory synapses and dendritic spines, while at the same time blocking inhibitory synapse upscaling. Furthermore, we identify the Neuroligin2 interacting molecule Mdga1 as a crucial target of miR-218-5p in the context of homeostatic upscaling of inhibitory synapses. By performing long-term electroencephalographic (EEG) recordings, we further revealed that local inhibition of miR-218-5p in the somatosensory cortex reduced local slow-wave activity (SWA) during non-rapid-eye-movement (NREM) sleep. In summary, this study uncovers miR-218-5p as a key player in coordinating inhibitory and excitatory synapses during homeostatic plasticity and sleep. Our findings contribute to a deeper understanding of how neural circuits maintain stability in the face of activity-induced perturbations, with potential implications for both physiological and pathological conditions. Significance StatementHomeostatic synaptic plasticity mechanisms evolved to keep neuronal firing rates within a physiological range in response to alterations in neural network activity. It has been proposed that similar mechanisms take place during sleep in a process that promotes memory consolidation and synaptic renormalization. In this study, posttranscriptional regulation of synaptic proteins by miR-218-5p has been identified to coordinate both excitatory and inhibitory synaptic scaling during activity-dependent homeostatic synaptic plasticity. Intriguingly, local inhibition of miR-218-5p in the cortex of mice resulted in reduced slow-wave activity, an EEG-signature of synchronous firing during non-rapid eye movement sleep and a hallmark correlate of sleep pressure. Overall, these findings propose a convergent, posttranscriptional mechanism to coordinate both excitatory and inhibitory synaptic strength in response to alterations in neuronal activity with potential implications for sleep.