伤害
脑啡肽
类阿片
免疫系统
细胞生物学
阿片肽
受体
神经科学
伤害感受器
阿片受体
生物
医学
免疫学
内科学
作者
Élora Midavaine,Beatriz C. Moraes,Jorge Benitez,Sian Rodriguez-Rosado,João M. Bráz,N. Kochhar,Walter L. Eckalbar,Lin Tian,Ana I. Domingos,John E. Pintar,Allan I. Basbaum,Sakeen W. Kashem
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2025-04-04
卷期号:388 (6742): 96-104
标识
DOI:10.1126/science.adq6531
摘要
T cells have emerged as orchestrators of pain amplification, but the mechanism by which T cells control pain processing is unresolved. We found that regulatory T cells (T reg cells) could inhibit nociception through a mechanism that was not dependent on their ability to regulate immune activation and tissue repair. Site-specific depletion or expansion of meningeal T reg cells (mT reg cells) in mice led to female-specific and sex hormone–dependent modulation of mechanical sensitivity. Specifically, mT reg cells produced the endogenous opioid enkephalin that exerted an antinociceptive action through the delta opioid receptor expressed by MrgprD + sensory neurons. Although enkephalin restrains nociceptive processing, it was dispensable for T reg cell–mediated immunosuppression. Thus, our findings uncovered a sexually dimorphic immunological circuit that restrains nociception, establishing T reg cells as sentinels of pain homeostasis.
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