Rivera Juan
Molecular Inflammation Section, Molecular Immunology and Inflammation Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, Maryland 20892-1820, USA.
Curr Opin Immunol. 2002 Dec;14(6):688-93. doi: 10.1016/s0952-7915(02)00396-5.
IgE-dependent activation of mast cells is central to the allergic response. The engagement of IgE-occupied receptors initiates a series of molecular events that cause the release of preformed, and de novo synthesis of, allergic mediators. Recent investigations demonstrate a critical role for non-enzymatic proteins that facilitate the activation and coordination of biochemical signals required for mast cell activation. Among these LAT, SLP-76 and Gab2 are critically important as adapters that facilitate events initiated by IgE receptor-dependent activation of Src family protein tyrosine kinases, Lyn and Fyn. An evaluation of the role of these adapters points to complementary but independent steps in early signaling and the possibility that preference for one or another adaptor complex may result in selective mast cell responses.
肥大细胞的IgE依赖性激活是过敏反应的核心。IgE占据的受体的结合引发了一系列分子事件,导致预先形成的过敏介质的释放以及从头合成。最近的研究表明,非酶蛋白在促进肥大细胞激活所需的生化信号的激活和协调方面起着关键作用。其中,LAT、SLP-76和Gab2作为衔接蛋白至关重要,它们促进由Src家族蛋白酪氨酸激酶Lyn和Fyn的IgE受体依赖性激活引发的事件。对这些衔接蛋白作用的评估指出了早期信号传导中互补但独立的步骤,以及偏好一种或另一种衔接蛋白复合物可能导致肥大细胞选择性反应的可能性。