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屋尘螨激活伤害感受器-肥大细胞簇以驱动 2 型皮肤炎症。

House dust mites activate nociceptor-mast cell clusters to drive type 2 skin inflammation.

机构信息

Unité de Différenciation Epithéliale et Autoimmunité Rhumatoïde, UMR 1056, INSERM, Université de Toulouse, Toulouse, France.

Department of Pathology, Stanford University School of Medicine, Stanford, CA, USA.

出版信息

Nat Immunol. 2019 Nov;20(11):1435-1443. doi: 10.1038/s41590-019-0493-z. Epub 2019 Oct 7.

Abstract

Allergic skin diseases, such as atopic dermatitis, are clinically characterized by severe itching and type 2 immunity-associated hypersensitivity to widely distributed allergens, including those derived from house dust mites (HDMs). Here we found that HDMs with cysteine protease activity directly activated peptidergic nociceptors, which are neuropeptide-producing nociceptive sensory neurons that express the ion channel TRPV1 and Tac1, the gene encoding the precursor for the neuropeptide substance P. Intravital imaging and genetic approaches indicated that HDM-activated nociceptors drive the development of allergic skin inflammation by inducing the degranulation of mast cells contiguous to such nociceptors, through the release of substance P and the activation of the cationic molecule receptor MRGPRB2 on mast cells. These data indicate that, after exposure to HDM allergens, activation of TRPV1Tac1 nociceptor-MRGPRB2 mast cell sensory clusters represents a key early event in the development of allergic skin reactions.

摘要

变应性皮肤疾病(如特应性皮炎)的临床特征为剧烈瘙痒和 2 型免疫相关的过敏反应,其广泛的过敏原包括屋尘螨(HDM)来源的过敏原。在这里,我们发现具有半胱氨酸蛋白酶活性的 HDM 可直接激活肽能伤害感受器,即表达离子通道 TRPV1 和 Tac1 的产生神经肽的伤害感受感觉神经元,Tac1 基因编码神经肽物质 P 的前体。活体成像和遗传方法表明,HDM 激活的伤害感受器通过释放物质 P 和激活肥大细胞上的阳离子分子受体 MRGPRB2,诱导与伤害感受器相邻的肥大细胞脱颗粒,从而驱动过敏性皮肤炎症的发展。这些数据表明,在接触 HDM 过敏原后,TRPV1Tac1 伤害感受器-MRGPRB2 肥大细胞感觉簇的激活代表过敏性皮肤反应发展的关键早期事件。

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