Interleukin-10 signaling in somatosensory neurons controls CCL2 release and inflammatory response

背根神经节 下调和上调 趋化因子 降钙素基因相关肽 促炎细胞因子 免疫学 小胶质细胞 细胞生物学 受体 生物 神经科学 炎症 化学 神经肽 感觉系统 内科学 医学 基因 生物化学
作者
Sabrina de Souza,Jesús Rosario Claudio,Jaewon Sim,Kufreobong E. Inyang,Andrew Dagenais,Karli Monahan,Beenhwa Grace Lee,Hariharan Ramakrishnan,Visha Parmar,Matan Geron,Grégory Scherrer,Joseph K. Folger,Geoffroy Laumet
出处
期刊:Brain Behavior and Immunity [Elsevier BV]
卷期号:116: 193-202 被引量:3
标识
DOI:10.1016/j.bbi.2023.12.013
摘要

Appropriate regulation of the inflammatory response is essential for survival. Interleukin-10 (IL-10), a well-known anti-inflammatory cytokine, plays a major role in controlling inflammation. In addition to immune cells, we previously demonstrated that the IL-10 receptor (IL-10R1) is expressed in dorsal root ganglion sensory neurons. There is emerging evidence that these sensory neurons contribute to immunoregulation, and we hypothesized that IL-10 signaling in dorsal root ganglion (DRG) neurons facilitates the regulation of the inflammatory response. We showed that mice that lack IL-10R1 specifically on advillin-positive neurons have exaggerated blood nitric oxide levels, spinal microglia activation, and cytokine upregulation in the spinal cord, liver, and gut compared to wild-type (WT) counterparts in response to systemic lipopolysaccharide (LPS) injection. Lack of IL-10R1 in DRG and trigeminal ganglion (TG) neurons also increased circulating and DRG levels of proinflammatory C–C motif chemokine ligand 2 (CCL2). Interestingly, analysis of published scRNA-seq data revealed that Ccl2 and Il10ra are expressed by similar types of DRG neurons; nonpeptidergic P2X purinoceptor (P2X3R + ) neurons. In primary cultures of DRG neurons, we demonstrated that IL-10R1 inhibits the production of CCL2, but not that of the neuropeptides substance P and calcitonin-gene related peptide (CGRP). Furthermore, our data indicate that ablation of Transient receptor potential vanilloid (TRPV)1 + neurons does not impact the regulation of CCL2 production by IL-10. In conclusion, we showed that IL-10 binds to its receptor on sensory neurons to downregulate CCL2 and contribute to immunoregulation by reducing the attraction of immune cells by DRG neuron-derived CCL2. This is the first evidence that anti-inflammatory cytokines limit inflammation through direct binding to receptors on sensory neurons. Our data also add to the growing literature that sensory neurons have immunomodulatory functions.

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