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Neuroimmune Activation Drives Multiple Brain States
Daria Tchessalova1, Caitlin Kelly Posillico2, Natalie Celia Tronson1,2
1Neuroscience Graduate Program, School of Medicine, University of Michigan, Ann Arbor, MI, United States.
Insights
Neuroimmune signaling influences memory, emotion, and cognition. Illness or injury can cause lasting changes in brain function and behavior by shifting the neuroimmune baseline.
Area of Science:
- Neuroscience
- Immunology
- Cognitive Science
Background:
- Neuroimmune signaling, involving microglia, astrocytes, and cytokines, is crucial for cognitive and emotional processes.
- Research is actively exploring how these interactions modulate behavior during and after illness or injury.
Purpose of the Study:
- To discuss neuroimmune activation as a mechanism for different behavioral states.
- To propose a continuum of neuroimmune states from homeostatic to chronic activation.
- To highlight the enduring impact of neuroimmune activation on neural function and behavior.
Main Methods:
- Discussing neuroimmune activation as a mechanism.
- Proposing a continuum of neuroimmune states.
- Identifying states via cytokine/glial patterns, behavior, and epigenetics.
Main Results:
- Neuroimmune activation triggers states that modulate cognition and emotion for adaptive behavior.
- Cognitive and mood impairments can persist post-illness due to lasting shifts in the homeostatic baseline.
- Distinct neuroimmune states can be identified multidimensionally.
Conclusions:
- Identifying neuroimmune states offers a framework for predicting vulnerability to memory, cognition, and emotion disorders.
- Understanding these states is key for predicting long-term consequences of illness or injury.
- This research provides a basis for understanding persistent deficits in neural function and behavior.
Abstract:
Neuroimmune signaling is increasingly identified as a critical component of neuronal processes underlying memory, emotion and cognition. The interactions of microglia and astrocytes with neurons and synapses, and the individual cytokines and immune signaling molecules that mediate these interactions are a current focus of much research. Here, we discuss neuroimmune activation as a mechanism triggering different states that modulate cognitive and affective processes to allow for appropriate behavior during and after illness or injury. We propose that these states lie on a continuum from a naïve homeostatic baseline state in the absence of stimulation, to acute neuroimmune activity and chronic activation. Importantly, consequences of illness or injury including cognitive deficits and mood impairments can persist long after resolution of immune signaling. This suggests that neuroimmune activation also results in an enduring shift in the homeostatic baseline state with long lasting consequences for neural function and behavior. Such different states can be identified in a multidimensional way, using patterns of cytokine and glial activation, behavioral and cognitive changes, and epigenetic signatures. Identifying distinct neuroimmune states and their consequences for neural function will provide a framework for predicting vulnerability to disorders of memory, cognition and emotion both during and long after recovery from illness.
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