Cady Carol T, Rice Jeffrey S, Ott Vanessa L, Cambier John C
Department of Immunology, University of Colorado Denver School of Medicine, Denver, CO, USA.
Immunol Rev. 2008 Aug;224:44-57. doi: 10.1111/j.1600-065X.2008.00663.x.
Numerous autoimmune and inflammatory disorders stem from the dysregulation of hematopoietic cell activation. The activity of inositol lipid and protein tyrosine phosphatases, and the receptors that recruit them, is critical for prevention of these disorders. Balanced signaling by inhibitory and activating receptors is now recognized to be an important factor in tuning cell function and inflammatory potential. In this review, we provide an overview of current knowledge of membrane proximal events in signaling by inhibitory/regulatory receptors focusing on structural and functional characteristics of receptors and their effectors Src homology 2 (SH2) domain-containing tyrosine phosphatase 1 and SH2 domain-containing inositol 5-phosphatase-1. We review use of new strategies to identify novel regulatory receptors and effectors. Finally, we discuss complementary actions of paired inhibitory and activating receptors, using Fc gammaRIIA and Fc gammaRIIB regulation human basophil activation as a prototype.
许多自身免疫性和炎症性疾病源于造血细胞激活的失调。肌醇脂质和蛋白酪氨酸磷酸酶及其招募的受体的活性对于预防这些疾病至关重要。现在人们认识到,抑制性和激活性受体的平衡信号传导是调节细胞功能和炎症潜能的一个重要因素。在这篇综述中,我们概述了目前关于抑制性/调节性受体信号传导中膜近端事件的知识,重点关注受体及其效应器含Src同源2(SH2)结构域的酪氨酸磷酸酶1和含SH2结构域的肌醇5-磷酸酶-1的结构和功能特征。我们回顾了使用新策略来鉴定新型调节性受体和效应器。最后,我们以FcγRIIA和FcγRIIB调节人嗜碱性粒细胞激活为原型,讨论配对的抑制性和激活性受体的互补作用。