Neuronal FcεRIα directly mediates ocular itch via IgE-immune complex in a mouse model of allergic conjunctivitis

被引：7

作者：

Cui, Huan ^{[1
]}

Liu, Fan ^{[2
]}

Fang, Yehong ^{[1
]}

Wang, Tao ^{[1
]}

Yuan, Bo ^{[1
]}

Ma, Chao ^{[1
,2
,3
]}

机构：

[1] Chinese Acad Med Sci, Dept Human Anat Histol & Embryol, Inst Basic Med Sci, Neurosci Ctr,Sch Basic Med,Peking Union Med Coll, Beijing, Peoples R China

[2] Chinese Acad Med Sci, Natl Human Brain Bank Dev & Funct, Inst Basic Med Sci, Sch Basic Med,Peking Union Med Coll, Beijing, Peoples R China

[3] Chinese Inst Brain Res, Beijing, Peoples R China

来源：

JOURNAL OF NEUROINFLAMMATION | 2022年 / 19卷 / 01期

基金：

中国国家自然科学基金;

关键词：

Ocular itch; Allergic conjunctivitis; Fc epsilon RI alpha; Sensory neuron; PRIMARY SENSORY NEURONS; MAST-CELLS; IMMUNOGLOBULIN-E; RECEPTOR-I; SIGNAL-TRANSDUCTION; EXPRESSION; OMALIZUMAB; HISTAMINE; BINDING; PAIN;

D O I：

10.1186/s12974-022-02417-x

中图分类号：

R392 [医学免疫学]; Q939.91 [免疫学];

学科分类号：

100102 ;

摘要：

Background: Classical understanding of allergic conjunctivitis (ACJ) suggests that ocular itch results from a mast cell-dependent inflammatory process. However, treatments that target inflammatory mediators or immune cells are often unsatisfying in relieving the stubborn itch symptom. This suggests that additional mechanisms are responsible for ocular itch in ACJ. In this study, we aim to determine the role of neuronal Fc epsilon RIa in allergic ocular itch. Methods: Calcium imaging was applied to observe the effect of IgE-immune complex in trigeminal neurons. Genomic Fc epsilon RIa knockout mice and adeno-associated virus (AAV) mediated sensory neuron Fc epsilon RIa knockdown mice were used in conjunction with behavioral tests to determine ocular itch. In addition, immunohistochemistry, Western blot and quantitative RT-PCR were used for in vitro experiments. Results: We found that Fc epsilon RI alpha was expressed in a subpopulation of conjunctiva sensory neurons. IgE-IC directly activated trigeminal neurons and evoked acute ocular itch without detectible conjunctival inflammation. These effects were attenuated in both a global Fc epsilon RIa-knockout mice and after sensory neuronal-specific Fc epsilon RIa-knockdown in the mouse trigeminal ganglion. In an ovalbumin (OVA) induced murine ACJ model, Fc epsilon RI alpha was found upregulated in conjunctiva-innervating CGRP+ sensory neurons. Sensory neuronal-specific knockdown of Fc epsilon RIa significantly alleviated ocular itch in the ACJ mice without affecting the immune cell infiltration and mast cell activation in conjunctiva. Although Fc epsilon RI alpha mRNA expression was not increased by IgE in dissociated trigeminal ganglion neurons, Fc epsilon RI alpha protein level was enhanced by IgE in a cycloheximide-resistance manner, with concordant enhancement of neuronal responses to IgE-IC. In addition, incremental sensitization gradually enhanced the expression of Fc epsilon RI alpha in small-sized trigeminal neurons and aggravated OVA induced ocular itch. Conclusions: Our study demonstrates that Fc epsilon RI alpha in pruriceptive neurons directly mediates IgE-IC evoked itch and plays an important role in ocular itch in a mouse model of ACJ. These findings reveal another axis of neuroimmune interaction in allergic itch condition independent to the classical IgE-mast cell pathway, and might suggest novel therapeutic strategies for the treatment of pruritus in ACJ and other immune-related disorders.

引用

页数：18