Modeling predicts a biochemical feedback mechanism underlying astrocyte calcium refractory periods

Astrocytes exhibit intracellular calcium fluctuations in response to neuronal activity. Repeated receptor stimulation can induce a transient suppression of calcium signaling-a refractory period-yet the underlying mechanisms and timescales of this phenomenon during behavior remain poorly understood. Here, we present a biophysically grounded computational model of astrocytic calcium signaling that incorporates a novel feedback mechanism mediated by conventional protein kinase C (cPKC) and predicts the refractory phenomenon. Unlike previous models developed in vitro, our model is directly validated using <i>in vivo</i> two-photon calcium imaging data from behaving mice. It closely recapitulates astrocytic calcium dynamics across both time and frequency domains, including the emergence of refractory periods and their negative correlation with inter-stimulus intervals. Simulations further predict the timing of recovery from refractory states, consistent with experimental observations. This work provides a mechanistic explanation for astrocytic refractory behavior and establishes a framework for integrating computational modeling with <i>in vivo</i> functional imaging.

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Publication Details

Journal
bioRxiv (Cold Spring Harbor Laboratory)
Published
2026-01-13
DOI
https://doi.org/10.64898/2026.01.12.699127
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
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article

Modeling predicts a biochemical feedback mechanism underlying astrocyte calcium refractory periods

Lin Tian, Nicholas A. Nelson, Mary Kaye Duff, James Cheng Peng et al.
bioRxiv (Cold Spring Harbor Laboratory)
Neuroscience and Neuropharmacology Research
article

Modeling predicts a biochemical feedback mechanism underlying astrocyte calcium refractory periods

Lin Tian, Nicholas A. Nelson, Mary Kaye Duff, James Cheng Peng, Daniela Duarte, Yizhi Wang, Katharina Merten, Axel Nimmerjahn, Guoqiang Yu, Yue Wang
article en

Abstract

Astrocytes exhibit intracellular calcium fluctuations in response to neuronal activity. Repeated receptor stimulation can induce a transient suppression of calcium signaling-a refractory period-yet the underlying mechanisms and timescales of this phenomenon during behavior remain poorly understood. Here, we present a biophysically grounded computational model of astrocytic calcium signaling that incorporates a novel feedback mechanism mediated by conventional protein kinase C (cPKC) and predicts the refractory phenomenon. Unlike previous models developed in vitro, our model is directly validated using <i>in vivo</i> two-photon calcium imaging data from behaving mice. It closely recapitulates astrocytic calcium dynamics across both time and frequency domains, including the emergence of refractory periods and their negative correlation with inter-stimulus intervals. Simulations further predict the timing of recovery from refractory states, consistent with experimental observations. This work provides a mechanistic explanation for astrocytic refractory behavior and establishes a framework for integrating computational modeling with <i>in vivo</i> functional imaging.

bioRxiv (Cold Spring Harbor Laboratory)
Salk Institute for Biological Studies (US), University of California San Diego (US), Chinese Institute for Brain Research (CN), Max Planck Florida Institute for Neuroscience (US), University of California, Davis (US), Virginia Tech (US), Tsinghua University (CN)
Openalex Percentile: Top 89%
Neuroscience and Neuropharmacology Research
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