bioRxiv Science⌕ Search

bioRxiv · 10.64898/2025.12.16.694668

Neuronal activity induces myelin voltage changes that reflect action potential dependent myelin potassium buffering

Abstract

Vertebrate axons can be wrapped by myelin produced by oligodendrocytes. This cellular interaction ensures fast and accurate propagation of action potentials, but the physiology of the myelin sheath is almost completely unknown. To investigate the physiology of the myelin sheath, we implemented an imaging strategy that allowed optical measurements of myelin membrane voltage, with the aim to identify physiological changes of the myelin membrane during neuronal firing. We expressed the genetically encoded voltage indicator ASAP3 in mouse oligodendrocytes in vivo and subsequently investigated myelin physiology by optically measuring myelin membrane voltage. We found that myelin depolarizes during neuronal activity, which is blocked by inhibiting neuronal action potentials. Pharmacological and knock-out experiments of Kir4.1 showed that potassium uptake channels mediate action potential induced depolarization. Blocking myelin dependent potassium uptake and direct application of high potassium to identified axons induced axonal initiated and antidromic propagating action potentials. Our study shows that myelin is not an electrically passive insulator, but exhibits ion dynamics and its physiological response is fine tuned to neuronal activity. By facilitating potassium removal during action potentials, myelin supports high precision axonal firing. Genetically encoded sensors are thus a useful tool to study physiological properties of myelin, inaccessible by classical techniques. HighlightsO_LIOptical imaging of myelin membrane potential C_LIO_LIMyelin sheaths exhibit depolarization in response to neuronal firing C_LIO_LIDepolarizations are partially mediated through Kir channels C_LIO_LIPotassium originates from axonal Kv channels C_LI

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Labarchede, M., Petrel, M., Battefeld, A.. 2025-12-17. Neuronal activity induces myelin voltage changes that reflect action potential dependent myelin potassium buffering. https://doi.org/10.64898/2025.12.16.694668

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

KEEP EXPLORING

Related preprints

Attention Across Scales: From Individual Variation to Social Hierarchies and Brain Networks in Semi-Free-Ranging Macaques

Attention is a fundamental brain function supporting perception, decision-making, and social behavior, and its dysfunction profoundly impairs daily life. It is both dynamic and stable, varying across observations and individuals, changing across the lifespan, and being shaped by social and environmental experience. Yet capturing this complexity remains a central challenge in neuroscience. Here, we integrated longitudinal behavioral assessments of semi-free-ranging macaques living in naturalistic social groups with resting-state fMRI. We quantified performance across days, ages, and social hierarchies and related it to intrinsic brain organization. Distinct attentional phenotypes emerged, including individuals with reduced attentional control. Performance followed an inverted-U lifespan trajectory, improving from childhood to adulthood before declining. Social status modulated attentional performance. Critically, nonlinear lifespan trajectories and associations with individual attentional differences were most clearly expressed in frontoparietal connectivity. Together, these findings reveal how sustained attention is organized across scales, providing a biological framework for its individual diversity, social modulation, and neural basis.

neuroscience↗

Decoding natural scenes from patterned optogenetic responses in mouse visual cortex

A central challenge in developing visual cortical prostheses is to determine how visual stimuli should be transformed into effective patterns of cortical stimulation. Although advances in stimulation technologies, including optogenetics, provide increasingly precise control over cortical activity, it remains unclear whether artificially evoked activity can reproduce the information content of naturally evoked visual representations. Here we establish a quantitative framework for evaluating visual encoding strategies by decoding cortical responses evoked by natural vision and patterned optogenetic stimulation. We developed a novel dual-modal paradigm in awake mice to bridge the gap between endogenous photostimulation and artificial network driving. By co-expressing the high-performance calcium indicator GCaMP6s and the red-shifted, ultra-sensitive opsin rsChRmine-oScarlet in the primary visual cortex (V1), we successfully translated dynamic natural movie frames into patterned, spatiotemporal optogenetic stimulation. Quantitative comparisons of macro-scale dynamics demonstrated that this patterned optogenetic injection evokes cortical states highly comparable and representationally aligned with those driven by actual visual photostimulation. To systematically evaluate the fidelity of these responses, we developed STAR, a deep learning model featuring spatial and temporal attention mechanisms, and successfully reconstructed the frames of natural movies from V1 signals under both experimental modalities. Collectively, our results demonstrate that complex sensory information can be both naturally encoded and synthetically injected into V1 circuits with high decoding fidelity. This work provides an empirical and computational proof-of-concept for intelligent, closed-loop biomimetic encoders, establishing a robust framework for next-generation cortical visual neuroprostheses and bidirectional brain-machine interfaces.

neuroscience↗

Why Is Spontaneous Blink Timing Informative? An Adaptive Scheduling Perspective

Spontaneous eye blinks have long been linked to cognitive processing, yet how task demands shape blink timing and its relationship to behavioral performance remains unclear. We examined spontaneous blink behavior in 576 adults performing two variants of the Continuous Performance Task (CPT). Blink occurrence and timing were most strongly modulated by the experimental condition in the more demanding CPT-AX task, whereas their association with response time was stronger in the CPT-X task, where more consistent blink timing predicted faster responses. This dissociation suggests that task structure changes not only blink behavior but also the behavioral relevance of blink timing. These findings are consistent with an adaptive scheduling account of spontaneous blinking and provide a conceptual framework for understanding when and why blink timing contains chronometric information about ongoing cognition.

neuroscience↗