组胺能
组胺
肥大细胞
前列腺素D2
受体
免疫球蛋白E
生物
免疫学
组胺H4受体
刺激
组胺受体
细胞生物学
药理学
抗体
组胺H2受体
内分泌学
敌手
生物化学
作者
James Meixiong,Michael Anderson,Nathachit Limjunyawong,Mark F Sabbagh,Eric Hu,Madison R. Mack,Landon K. Oetjen,Fang Wang,Brian Kim,Xinzhong Dong
出处
期刊:Immunity
[Elsevier]
日期:2019-04-23
卷期号:50 (5): 1163-1171.e5
被引量:256
标识
DOI:10.1016/j.immuni.2019.03.013
摘要
Classical itch studies have focused on immunoglobulin E (IgE)-mediated mast cell activation and histamine release. Recently, members of the Mas-related G-protein-coupled receptor (Mrgpr) family have been identified as mast cell receptors, but their role in itch is unclear. Here, we report that mast cell activation via Mrgprb2 evoked non-histaminergic itch in mice independently of the IgE-Fc epsilon RI (FcεRI)-histamine axis. Compared with IgE-FcεRI stimulation, Mrgprb2 activation of mast cells was distinct in both released substances (histamine, serotonin, and tryptase) and the pattern of activated itch-sensory neurons. Mrgprb2 deficiency decreased itch in multiple preclinical models of allergic contact dermatitis (ACD), a pruritic inflammatory skin disorder, and both mast cell number and PAMP1-20 concentrations (agonist of the human Mrgprb2 homolog, MRGPRX2) were increased in human ACD skin. These findings suggest that this pathway may represent a therapeutic target for treating ACD and mast-cell-associated itch disorders in which antihistamines are ineffective.
科研通智能强力驱动
Strongly Powered by AbleSci AI