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Updated: May 3, 2026

Isolation of Cortical Microglia with Preserved Immunophenotype and Functionality From Murine Neonates
Published on: January 30, 2014
Microglia surveillance is directed toward neuron activation during sustained intracortical microstimulation
C Preszler1,2, K Stieger1,2, K Chen1,2
1Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States of America.
Abstract:
Objective.Intracortical microstimulation (ICMS) is a widely used tool for neuroprostheses, but its long-term efficacy is often limited by foreign body response and neuroinflammatory responses at the electrode-tissue interface. Microglia orchestrate neuroinflammation and regulate synaptic plasticity, and low-frequency stimulation has been shown to promote anti-inflammatory microglial phenotypes.Approach.We investigated how 10 Hz ICMS influences microglia-neuron interactions during the first three days post-implantation usingin vivotwo-photon imaging in Cx3cr1-GFP/jRGECO1a mice. Microglial motility, morphology, and process orientation were tracked relative to electrode placement and neuronal calcium activity (measured as change in fluorescence, ΔF/F).Main results.A 1 h session of 10 Hz ICMS did not induce overt classical morphological activation of microglia but robustly increased process motility, with extensions dynamically tracking neurons showing early activation or subsequent functional suppression. By post-implantation Day 2, microglial processes were significantly more likely to engage neurons with high early calcium responses after stimulation onset (mean orientation angle: 74.3° ± 11.8°), but this engagement shifted during prolonged stimulation (117.0° ± 9.2°,p= 0.0017), indicating context-dependent interactions. Contact frequency scaled with neuronal adaptation profiles, and neurons exhibiting depressed activity received the most contacts immediately after implantation (1.2 ± 0.3 contacts,p= 0.046).Significance.These findings reveal stimulus-associated, neuron-dependent surveillance behaviors of microglia during early post-implantation ICMS and suggest that microglia actively participate in short-term modulation of stimulated cortical circuits.
Insights
Low-frequency intracortical microstimulation (ICMS) increases microglial process motility, enabling dynamic tracking of neuronal activity. Microglia actively engage neurons, influencing short-term circuit modulation after electrode implantation.
Area of Science:
- Neuroscience
- Biomedical Engineering
- Immunology
Background:
- Intracortical microstimulation (ICMS) is crucial for neuroprosthetics but faces limitations due to neuroinflammation and foreign body responses at the electrode-tissue interface.
- Microglia are key regulators of neuroinflammation and synaptic plasticity.
- Low-frequency stimulation may promote anti-inflammatory microglial phenotypes.
Purpose of the Study:
- To investigate the influence of 10-Hz ICMS on microglia-neuron interactions during the initial three days post-implantation.
- To understand how microglial behavior (motility, morphology, process orientation) relates to neuronal activity and electrode placement.
Main Methods:
- In vivo two-photon imaging was employed in Cx3cr1-GFP/jRGECO1a mice.
- Microglial motility, morphology, and process orientation were tracked relative to electrode placement.
- Neuronal calcium activity was measured as changes in fluorescence (ΔF/F).
Main Results:
- 10-Hz ICMS increased microglial process motility without inducing overt classical activation.
- Microglial processes dynamically tracked neurons exhibiting early activation or functional suppression.
- Microglial engagement with neurons shifted during prolonged stimulation, indicating context-dependent interactions.
- Contact frequency correlated with neuronal adaptation, with depressed neurons receiving more contacts post-implantation.
Conclusions:
- Microglia exhibit stimulus-associated, neuron-dependent surveillance behaviors following ICMS.
- These findings suggest microglia actively modulate stimulated cortical circuits in the short term.
- Understanding these interactions is vital for optimizing neuroprosthetic efficacy and minimizing inflammatory responses.
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