Department of Basic and Translational Sciences, University of Pennsylvania, School of Dental Medicine, Philadelphia, Pa.
Department of Basic and Translational Sciences, University of Pennsylvania, School of Dental Medicine, Philadelphia, Pa.
J Allergy Clin Immunol. 2021 Aug;148(2):293-308. doi: 10.1016/j.jaci.2021.03.049. Epub 2021 May 4.
Cutaneous mast cells (MCs) express Mas-related G protein-coupled receptor-X2 (MRGPRX2; mouse ortholog MrgprB2), which is activated by an ever-increasing number of cationic ligands. Antimicrobial host defense peptides (HDPs) generated by keratinocytes contribute to host defense likely by 2 mechanisms, one involving direct killing of microbes and the other via MC activation through MRGPRX2. However, its inappropriate activation may cause pseudoallergy and likely contribute to the pathogenesis of rosacea, atopic dermatitis, allergic contact dermatitis, urticaria, and mastocytosis. Gain- and loss-of-function missense single nucleotide polymorphisms in MRGPRX2 have been identified. The ability of certain ligands to serve as balanced or G protein-biased agonists has been defined. Small-molecule HDP mimetics that display both direct antimicrobial activity and activate MCs via MRGPRX2 have been developed. In addition, antibodies and reagents that modulate MRGPRX2 expression and signaling have been generated. In this article, we provide a comprehensive update on MrgprB2 and MRGPRX2 biology. We propose that harnessing MRGPRX2's host defense function by small-molecule HDP mimetics may provide a novel approach for the treatment of antibiotic-resistant cutaneous infections. In contrast, MRGPRX2-specific antibodies and inhibitors could be used for the modulation of allergic and inflammatory diseases that are mediated via this receptor.
皮肤肥大细胞 (MCs) 表达 Mas 相关 G 蛋白偶联受体 -X2 (MRGPRX2; 小鼠同源物 MrgprB2),它被越来越多的阳离子配体激活。角蛋白细胞产生的抗菌宿主防御肽 (HDP) 通过两种机制有助于宿主防御,一种涉及直接杀死微生物,另一种通过 MC 激活通过 MRGPRX2。然而,其不适当的激活可能导致假性过敏,并可能导致酒渣鼻、特应性皮炎、变应性接触性皮炎、荨麻疹和肥大细胞增多症的发病机制。已经确定了 MRGPRX2 中的获得功能和丧失功能错义单核苷酸多态性。某些配体作为平衡或 G 蛋白偏向激动剂的能力已经得到定义。已经开发出显示直接抗菌活性并通过 MRGPRX2 激活 MC 的小分子 HDP 模拟物。此外,还生成了调节 MRGPRX2 表达和信号的抗体和试剂。在本文中,我们提供了关于 MrgprB2 和 MRGPRX2 生物学的全面更新。我们提出,通过小分子 HDP 模拟物利用 MRGPRX2 的宿主防御功能可能为治疗抗生素耐药性皮肤感染提供一种新方法。相比之下,MRGPRX2 特异性抗体和抑制剂可用于调节通过该受体介导的过敏和炎症性疾病。