Search bioRxiv⌕ Search

bioRxiv · 10.1101/2025.04.25.647197

More running causes more ocular dominance plasticity in mouse primary visual cortex: new gated running wheel setup allows to quantify individual running behaviour of group-housed mice

Abstract

Environmental enrichment boosts neuronal plasticity of standard-cage raised (SC) mice. Since it becomes increasingly more important to track individual mouse behaviours and its influence on brain plasticity, we designed a gated running wheel (gRW) setup allowing to correlate wheel running with neuronal plasticity, using the established paradigm of ocular dominance (OD)-plasticity after monocular deprivation (MD). After SC-rearing until adulthood (>P110), group-housed mice were transferred to gRW cages, that provided an additional running wheel compartment for tracking individual wheel activity via implanted RFID chips. Notably, individual running parameters varied enormously: mice ran from close to 0 to [~]20 km across the 7 days of gRW experience, with on average running 0-3.96 km in 0-3.85 h/d and running bouts lasting from <1 up to 10 min, while running at a speed of 6-26 cm/s. OD-plasticity in V1 after 7 days of MD in the gRW was visualized using intrinsic signal optical imaging, and compared to control gRW-mice without MD via calculation of an OD-index. Most, notably - while wheel running enabled OD-plasticity -individual running parameters correlated with individual OD-indices after MD: Mice running longer distances, for longer time, at higher speeds and with longer and more frequent bouts displayed more experience-dependent V1-plasticity. In turn, a composite measure of overall running wheel activity derived from principal component analysis of running parameters accounted for 65% of inter-individual variability of OD-index following MD. Together our study demonstrates that interindividual variability of running behaviour is high, and mice intrinsically motivated to run more show enhanced V1-plasticity, underscoring the huge importance of analysing individual behavioural parameters together with any measure of brain plasticity. End Graphical abstract With our newly developed gated running wheel setup, we observed a striking correlation between individual running activity, and a measure of experience dependent plasticity in mouse primary visual cortex. More running caused more plasticity: running speed, running distance, total running time, number of running bouts and bout duration all correlated with a measure of visual cortical plasticity, the ocular dominance index. Thus, our observations add to the growing body of evidence that individual behavioural choices strongly affect individual brain plasticity. O_FIG O_LINKSMALLFIG WIDTH=149 HEIGHT=200 SRC="FIGDIR/small/647197v2_ufig1.gif" ALT="Figure 1"> View larger version (21K): org.highwire.dtl.DTLVardef@e1045dorg.highwire.dtl.DTLVardef@e5af90org.highwire.dtl.DTLVardef@1693a46org.highwire.dtl.DTLVardef@170ec3d_HPS_FORMAT_FIGEXP M_FIG C_FIG

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Schoene, C., Sathiyamani, J. S., Guranda, M., Schnurbusch, N., Loewel, S.. 2025-04-26. More running causes more ocular dominance plasticity in mouse primary visual cortex: new gated running wheel setup allows to quantify individual running behaviour of group-housed mice. https://doi.org/10.1101/2025.04.25.647197

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

A Mechanistic Account of Dedifferentiation in the Aging Visual System

To uncover the mechanisms of age-related dedifferentiation, we simulated neural degradation in a computational model of the ventral visual stream. Severing connections or adding noise, whether in inferotemporal cortex (IT) or upstream, reduced IT differentiation, indicating that dedifferentiation need not originate locally. Degrading peripheral V1, which preferentially drove place-selective IT neurons, selectively reduced place differentiation, a candidate mechanism for the stronger place dedifferentiation reported in aging.

neuroscience↗

Reusing pipettes in Patch-seq: a foundation for automated multimodal profiling

Patch-seq is a technique for single-cell multimodal characterization. It combines whole-cell electrophysiology, single-cell transcriptomics, and morphological reconstruction in single neurons. Patch-seq morphologies are a critical bridge among cell types, genes, physiology, and large-scale connectivity platforms such as EM connectomes and single-cell-resolution projectomes. However, patch-seq experimental complexity and operator dependence limit throughput. Automation could enable scalable Patch-seq but requires procedural adaptations, including detergent-based pipette cleaning, robotic nucleus extraction and collection. The impact of these automations on Patch-seq quality has not been systematically evaluated. Here, we show that each of these modifications preserves or improves key Patch-seq outcomes. Automated nucleus extraction performs comparably to, or better than, expert manual operation, preserving key RNA and morphological metrics. Detergent-cleaned, reused pipettes supported a viable sealing success rate across multiple cleaning cycles and preserved electrophysiological quality and transcriptomic yield without introducing excess contamination. Sonication effectively allows collection of nuclear material without damaging RNA and supports subsequent pipette cleaning and reuse. Enhanced automated sealing and break-in procedures increased throughput regardless of brain region, cell type or species. Together, these results validate the core procedural adaptations required for automated Patch-seq and establish a foundation for high-throughput, standardized multimodal single-cell characterization.

neuroscience↗

Development of direction selectivity in the Xenopus tadpole optic tectum and midbrain tegmentum

Detecting motion direction is a fundamental function performed by direction selective (DS) neurons. DS neurons in the optic tectum (superior colliculus in mammals) enable the tracking of moving objects. DS neurons of the accessory optic system support reflexive eye / head movements that stabilize gaze during self-motion. By developmental stage 48 (10 days postfertilization), Xenopus tadpoles display visually guided behaviors that require both types of DS neurons. Our previous work has shown that these two regions are not only functionally distinct but also follow different developmental programs. Here we characterized and compared how direction selectivity develops in both visual processing centers. Using in vivo electrophysiological recordings during moving bar visual stimulation, we measured DS synaptic inputs and spiking outputs in both regions across three key developmental stages of the retinotectal projection. Tegmental neurons were direction selective ab initio, and both input and output tuning remained stable across development. Tectal neurons were observed to receive DS inputs early, and their input selectivity also remained stable across development. However, their spiking output grew substantially more DS at the later developmental stage. This was due at least in part to a naturally occurring decrease in intrinsic excitability which preferentially dampened overall spike rates, but especially in response to the non-preferred direction of motion, thereby increasing direction selectivity. These results reveal distinct developmental trajectories in parallel visual pathways. Tegmental direction selectivity is established early and stays stable, whereas tectal output tuning sharpens during development through a decrease in intrinsic excitability.

neuroscience↗