Tatemoto Kazuhiko, Nozaki Yuko, Tsuda Ryoko, Konno Shinobu, Tomura Keiko, Furuno Masahiro, Ogasawara Hiroyuki, Edamura Koji, Takagi Hideo, Iwamura Hiroyuki, Noguchi Masato, Naito Takayuki
Department of Molecular Physiology, Institute for Molecular and Cellular Regulation, Gunma University, Maebashi 371-8512, Japan.
Biochem Biophys Res Commun. 2006 Nov 3;349(4):1322-8. doi: 10.1016/j.bbrc.2006.08.177. Epub 2006 Sep 8.
Mast cells play a central role in inflammatory and allergic reactions by releasing inflammatory mediators through two main pathways, immunoglobulin E-dependent and -independent activation. In the latter, mast cells are activated by a diverse range of basic molecules, including peptides and amines such as substance P, neuropeptide Y, and compound 48/80. These secretagogues are thought to activate the G proteins in mast cells through a receptor-independent mechanism. Here, we report that the basic molecules activate G proteins through the Mas-related gene (Mrg) receptors on mast cells, leading to mast cell degranulation. We suggest that one of the Mrg receptors, MrgX2, has an important role in regulating inflammatory responses to non-immunological activation of human mast cells.
肥大细胞在炎症和过敏反应中发挥核心作用,通过两条主要途径释放炎症介质,即免疫球蛋白E依赖性和非依赖性激活途径。在后者中,肥大细胞被多种碱性分子激活,包括肽和胺,如P物质、神经肽Y和化合物48/80。这些促分泌剂被认为通过一种不依赖受体的机制激活肥大细胞中的G蛋白。在此,我们报告这些碱性分子通过肥大细胞上的Mas相关基因(Mrg)受体激活G蛋白,导致肥大细胞脱颗粒。我们认为Mrg受体之一MrgX2在调节人类肥大细胞非免疫激活的炎症反应中起重要作用。