Syed Meesum, Kammala Ananth K, Callahan Brianna, Oskeritzian Carole A, Subramanian Hariharan
Department of Physiology, Michigan State University, East Lansing, MI 48824, United States.
Department of Pathology, Microbiology and Immunology, School of Medicine, University of South Carolina, Columbia, SC 29208, United States.
Cell Immunol. 2021 Oct;368:104422. doi: 10.1016/j.cellimm.2021.104422. Epub 2021 Aug 8.
MAS related G-protein coupled receptor X2 (MRGPRX2) is a G-protein coupled receptor (GPCR) expressed in human mast cells that has been implicated to play an important role in causing pseudo-allergic reactions as well as exacerbating inflammation during asthma and other allergic diseases. Lactic acid, a byproduct of glucose metabolism, is abundantly present in inflamed tissues and has been shown to regulate functions of several immune cells. Because the endogenous ligands for MRGPRX2 (substance P and LL-37) are elevated during pathologic conditions, such as cancer and asthma, and given that lactic acid levels are also enhanced in these patients, we explored the role of lactic acid in regulating mast cells response via MRGPRX2 and MrgprB2, the mouse orthologue of the human receptor. We found that lactic acid suppressed both the early (Ca mobilization and degranulation) and late (chemokine/cytokine release) phases of mast cell activation; this data was confirmed in LAD2, human skin and mouse peritoneal mast cells. In LAD2 cells, the reduction in degranulation and chemokine/cytokine production mediated by lactic acid was dependent on pH. In agreement with our in vitro studies, lactic acid also reduced passive systemic anaphylaxis to compound 48/80 (a known MRGPRX2/MrgprB2 ligand) and skin inflammation in a mouse model of rosacea that is dependent on MrgprB2 expression on skin mast cells. Our data thus suggest that lactic acid may serve to inhibit mast cell-mediated inflammation during asthma and reduce immune response during cancer by affecting mast cell activation through MRGPRX2.
与MAS相关的G蛋白偶联受体X2(MRGPRX2)是一种在人肥大细胞中表达的G蛋白偶联受体(GPCR),据认为在引起类过敏反应以及在哮喘和其他过敏性疾病中加剧炎症方面发挥重要作用。乳酸是葡萄糖代谢的副产物,大量存在于炎症组织中,并已显示出可调节多种免疫细胞的功能。由于MRGPRX2的内源性配体(P物质和LL-37)在诸如癌症和哮喘等病理状况下会升高,并且鉴于这些患者的乳酸水平也会升高,我们探讨了乳酸通过MRGPRX2和MrgprB2(人类受体的小鼠同源物)调节肥大细胞反应的作用。我们发现乳酸抑制了肥大细胞激活的早期(钙动员和脱颗粒)和晚期(趋化因子/细胞因子释放)阶段;这一数据在LAD2、人皮肤和小鼠腹膜肥大细胞中得到了证实。在LAD2细胞中,乳酸介导的脱颗粒和趋化因子/细胞因子产生的减少取决于pH值。与我们的体外研究一致,在酒渣鼻小鼠模型中,乳酸还减少了对化合物48/80(一种已知的MRGPRX2/MrgprB2配体)的被动全身过敏反应以及皮肤炎症,该反应依赖于皮肤肥大细胞上的MrgprB2表达。因此,我们的数据表明,乳酸可能通过MRGPRX2影响肥大细胞激活,从而在哮喘期间抑制肥大细胞介导的炎症,并在癌症期间降低免疫反应。