Localization of brain neuronal IL-1R1 reveals specific neural circuitries responsive to immune signaling

Interleukin-1 (IL-1) is a pro-inflammatory cytokine that exerts a wide range of neurological and immunological effects throughout the central nervous system (CNS) and is associated with the etiology of affective and cognitive disorders. The cognate receptor for IL-1, Interleukin-1 Receptor Type 1 (IL-1R1), is primarily expressed on non-neuronal cells (e.g., endothelial cells, choroidal cells, ventricular ependymal cells, astrocytes, etc.) throughout the brain. However, the presence and distribution of neuronal IL-1R1 (nIL-1R1) has been controversial. Here, for the first time, a novel genetic mouse line that allows for the visualization of IL-1R1 mRNA and protein expression (Il1r1<sup>GR/GR</sup>) was used to map all brain nuclei and determine the neurotransmitter systems which express nIL-1R1 in adult male mice. The direct responsiveness of nIL-1R1-expressing neurons to both inflammatory and physiological levels of IL-1β in vivo was tested. Neuronal IL-1R1 expression across the brain was found in discrete glutamatergic and serotonergic neuronal populations in the somatosensory cortex, piriform cortex, dentate gyrus, and dorsal raphe nucleus. Glutamatergic nIL-1R1 comprises most of the nIL-1R1 expression and, using Vglut2-Cre-Il1r1<sup>r/r</sup> mice, which restrict IL-1R1 expression to only glutamatergic neurons, an atlas of glutamatergic nIL-1R1 expression across the brain was generated. Analysis of functional outputs of these nIL-1R1-expressing nuclei, in both Il1r1<sup>GR/GR</sup> and Vglut2-Cre-Il1r1<sup>r/r</sup> mice, reveals IL-1R1<sup>+</sup> nuclei primarily relate to sensory detection, processing, and relay pathways, mood regulation, and spatial/cognitive processing centers. Intracerebroventricular (i.c.v.) injections of IL-1 (20 ng) induces NFκB signaling in IL-1R1<sup>+</sup> non-neuronal cells but not in IL-1R1<sup>+</sup> neurons, and in Vglut2-Cre-Il1r1<sup>r/r</sup> mice IL-1 did not change gene expression in the dentate gyrus of the hippocampus (DG). GO pathway analysis of spatial RNA sequencing 1mo following restoration of nIL-1R1 in the DG neurons reveals IL-1R1 expression downregulates genes related to both synaptic function and mRNA binding while increasing select complement markers (C1ra, C1qb). Further, DG neurons exclusively express an alternatively spliced IL-1R Accessory protein isoform (IL-1RAcPb), a known synaptic adhesion molecule. Altogether, this study reveals a unique network of neurons that can respond directly to IL-1 via nIL-1R1 through non-autonomous transcriptional pathways; earmarking these circuits as potential neural substrates for immune signaling-triggered sensory, affective, and cognitive disorders.

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Journal
Journal of Neuroinflammation
Published
2024-11-19
DOI
https://doi.org/10.1186/s12974-024-03287-1
Citations
17
Primary Topic
Neuroinflammation and Neurodegeneration Mechanisms
Type
article
Field-Weighted Citation Impact
4.21

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article

Localization of brain neuronal IL-1R1 reveals specific neural circuitries responsive to immune signaling

Alex C. Nusstein, Samantha McGovern, Ning Quan, Daniel B. McKim et al.
17 citations
Journal of Neuroinflammation
Neuroinflammation and Neurodegeneration Mechanisms
4.21
article

Localization of brain neuronal IL-1R1 reveals specific neural circuitries responsive to immune signaling

Alex C. Nusstein, Samantha McGovern, Ning Quan, Daniel B. McKim, Paula A. Gajewski-Kurdziel, Jonathan P. Godbout, Jasmine Yip, M. Smirnova, Randy Blakely, Marianne C. Monet, James Ellis, Andrew Crider, Trey Floyd, Daniel P. Nemeth, Rohit R. Atluri, Damon J. DiSabato, John F. Sheridan, Kristina G. Witcher, Anu Herd, Haichen Niu, Xiaoyu Liu, Qi Zhang, Braedan Oliver, G. C. Maxey, Matt Scott Schrier
article en
17 citations

Abstract

Interleukin-1 (IL-1) is a pro-inflammatory cytokine that exerts a wide range of neurological and immunological effects throughout the central nervous system (CNS) and is associated with the etiology of affective and cognitive disorders. The cognate receptor for IL-1, Interleukin-1 Receptor Type 1 (IL-1R1), is primarily expressed on non-neuronal cells (e.g., endothelial cells, choroidal cells, ventricular ependymal cells, astrocytes, etc.) throughout the brain. However, the presence and distribution of neuronal IL-1R1 (nIL-1R1) has been controversial. Here, for the first time, a novel genetic mouse line that allows for the visualization of IL-1R1 mRNA and protein expression (Il1r1<sup>GR/GR</sup>) was used to map all brain nuclei and determine the neurotransmitter systems which express nIL-1R1 in adult male mice. The direct responsiveness of nIL-1R1-expressing neurons to both inflammatory and physiological levels of IL-1β in vivo was tested. Neuronal IL-1R1 expression across the brain was found in discrete glutamatergic and serotonergic neuronal populations in the somatosensory cortex, piriform cortex, dentate gyrus, and dorsal raphe nucleus. Glutamatergic nIL-1R1 comprises most of the nIL-1R1 expression and, using Vglut2-Cre-Il1r1<sup>r/r</sup> mice, which restrict IL-1R1 expression to only glutamatergic neurons, an atlas of glutamatergic nIL-1R1 expression across the brain was generated. Analysis of functional outputs of these nIL-1R1-expressing nuclei, in both Il1r1<sup>GR/GR</sup> and Vglut2-Cre-Il1r1<sup>r/r</sup> mice, reveals IL-1R1<sup>+</sup> nuclei primarily relate to sensory detection, processing, and relay pathways, mood regulation, and spatial/cognitive processing centers. Intracerebroventricular (i.c.v.) injections of IL-1 (20 ng) induces NFκB signaling in IL-1R1<sup>+</sup> non-neuronal cells but not in IL-1R1<sup>+</sup> neurons, and in Vglut2-Cre-Il1r1<sup>r/r</sup> mice IL-1 did not change gene expression in the dentate gyrus of the hippocampus (DG). GO pathway analysis of spatial RNA sequencing 1mo following restoration of nIL-1R1 in the DG neurons reveals IL-1R1 expression downregulates genes related to both synaptic function and mRNA binding while increasing select complement markers (C1ra, C1qb). Further, DG neurons exclusively express an alternatively spliced IL-1R Accessory protein isoform (IL-1RAcPb), a known synaptic adhesion molecule. Altogether, this study reveals a unique network of neurons that can respond directly to IL-1 via nIL-1R1 through non-autonomous transcriptional pathways; earmarking these circuits as potential neural substrates for immune signaling-triggered sensory, affective, and cognitive disorders.

Journal of NeuroinflammationVol. 21(1)
University of Illinois Urbana-Champaign (US), Xuzhou Medical College (CN), Max Planck Florida Institute for Neuroscience (US), Institute for Behavioral Medicine (US), The Ohio State University (US), Florida Atlantic University (US), University of Toledo (US)
International Max Planck Research School for Advanced Methods in Process and Systems Engineering, National Institute of Mental Health, National Institute of Neurological Disorders and Stroke, National Institute of Dental and Craniofacial Research
Zero hunger
Openalex Percentile: Top 5%
Neuroinflammation and Neurodegeneration Mechanisms
4.21
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