先天性淋巴细胞
背根神经节
伤害
免疫系统
外周神经系统
生物
神经科学
炎症
免疫学
神经系统
表型
受体
人口
坐骨神经
外围设备
先天免疫系统
脊髓
医学
中枢神经系统
信号转导
自主神经系统
伤害感受器
免疫
后肢
功能(生物学)
解剖
细胞生物学
TRPV1型
作者
Divija Deshpande,Laura Velleman,Janna Schmitz,Patrycja M. Forster,Christian Schinke,Sotiria Boulekou,Henning Peter Düsedau,Susanne M. Krug,T. Mertens,Xuemei Gao,Caio Andreeta Figueiredo,Katja J. Jarick,Thomas Plum,Nele Sterczyk,Pierre S. Leclère,Sofia Helfrich,Anke Tappe‐Theodor,Katja Kotsch,Johannes Steffen,David Voehringer
出处
期刊:Science immunology
[American Association for the Advancement of Science]
日期:2025-09-26
卷期号:10 (111): eadp7092-eadp7092
被引量:4
标识
DOI:10.1126/sciimmunol.adp7092
摘要
The peripheral nervous system (PNS) is involved in nociception and gait. The contribution of PNS-resident immune cells to these functions is not fully understood. We identified group 2 innate lymphoid cells (ILC2s) as a distinct immune cell population resident in the PNS, with a unique gene profile facilitating neuron-ILC2 cross-talk. ILC2-deficient mice display PNS dysfunction (hypersensitivity and gait anomalies). These functional deficits are attributed to structural abnormalities in the sciatic nerves of ILC2-deficient mice. ILC2s communicate with dorsal root ganglion neurons via the interleukin-13 (IL-13) signaling pathway to maintain nerve structure and pain thresholds. Loss of the shared IL-4/IL-13 receptor (IL-4R/IL-13R) in neurons results in a phenotype similar to ILC2-deficient mice. Intrathecally administered IL-13 rescues hypersensitivity and gait defects in ILC2-deficient mice, which suggests that this signaling pathway may be therapeutically important. This work therefore identifies a function for ILC2s in regulating the nerve structural integrity and nociceptive functions of the PNS.
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