The Dorsal Root Ganglia: From a Neuronal Relay to a Sensory Organ

Somatosensory ganglia are often cast as passive relays, yet growing evidence shows the dorsal root ganglion (DRG) is a specialized sensory-immune organ. In the DRG, perineuronal and perivascular units act as sentinels that detect danger and calibrate immune tone. A permeable, macrophage-guarded blood-DRG barrier admits systemic cues, while neuron-glia microdomains set sensory gain and help restore homeostasis. Throughout the organ, neurons, glia, and vascular-stromal cells share immune receptors, enabling coordinated responses to infection, inflammation, and autoimmunity. In turn, neuronal signals reshape vascular tone and leukocyte trafficking, whereas immune mediators can promote recovery or drive pathology. Single-cell and spatial atlases reveal regenerative programs and zonation that organize these circuits. Together, these insights reframe the DRG as an integrator linking immune state to sensory encoding and pain. Preserving DRG structure-by fortifying barriers, stabilizing glial buffering, and steering macrophages toward resolution-could blunt maladaptive neuroimmune interactions and enable durable pain relief without compromising host defense.

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Publication Details

Journal
Annual Review of Neuroscience
Published
2026-03-20
DOI
https://doi.org/10.1146/annurev-neuro-102124-034329
Primary Topic
Vagus Nerve Stimulation Research
Type
article
Field-Weighted Citation Impact
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article

The Dorsal Root Ganglia: From a Neuronal Relay to a Sensory Organ

Harald Lund, Sébastien Talbot, Karen O. Dixon, Tuany Eichwald et al.
Annual Review of Neuroscience
Vagus Nerve Stimulation Research
article

The Dorsal Root Ganglia: From a Neuronal Relay to a Sensory Organ

Harald Lund, Sébastien Talbot, Karen O. Dixon, Tuany Eichwald, Linda Kaupp, Anais Roger, Elisa Preto
article en

Abstract

Somatosensory ganglia are often cast as passive relays, yet growing evidence shows the dorsal root ganglion (DRG) is a specialized sensory-immune organ. In the DRG, perineuronal and perivascular units act as sentinels that detect danger and calibrate immune tone. A permeable, macrophage-guarded blood-DRG barrier admits systemic cues, while neuron-glia microdomains set sensory gain and help restore homeostasis. Throughout the organ, neurons, glia, and vascular-stromal cells share immune receptors, enabling coordinated responses to infection, inflammation, and autoimmunity. In turn, neuronal signals reshape vascular tone and leukocyte trafficking, whereas immune mediators can promote recovery or drive pathology. Single-cell and spatial atlases reveal regenerative programs and zonation that organize these circuits. Together, these insights reframe the DRG as an integrator linking immune state to sensory encoding and pain. Preserving DRG structure-by fortifying barriers, stabilizing glial buffering, and steering macrophages toward resolution-could blunt maladaptive neuroimmune interactions and enable durable pain relief without compromising host defense.

Annual Review of Neuroscience
University of Basel (CH), Queen's University (CA), Karolinska Institutet (SE)
Openalex Percentile: Top 32%
Vagus Nerve Stimulation Research
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