Getahun Andrew, Cambier John C
Department of Immunology and Microbiology, University of Colorado School of Medicine, Aurora, CO, USA.
Immunol Rev. 2015 Nov;268(1):66-73. doi: 10.1111/imr.12336.
Receptors for immunoglobulin Fc regions play multiple critical roles in the immune system, mediating functions as diverse as phagocytosis, triggering degranulation of basophils and mast cells, promoting immunoglobulin class switching, and preventing excessive activation. Transmembrane signaling associated with these functions is mediated primarily by two amino acid sequence motifs, ITAMs (immunoreceptor tyrosine-based activation motifs) and ITIMs (immunoreceptor tyrosine-based inhibition motifs) that act as the receptors' interface with activating and inhibitory signaling pathways, respectively. While ITAMs mobilize activating tyrosine kinases and their consorts, ITIMs mobilize opposing tyrosine and inositol-lipid phosphatases. In this review, we will discuss our current understanding of signaling by these receptors/motifs and their sometimes blurred lines of function.
免疫球蛋白Fc区域受体在免疫系统中发挥多种关键作用,介导如吞噬作用、触发嗜碱性粒细胞和肥大细胞脱颗粒、促进免疫球蛋白类别转换以及防止过度激活等多种功能。与这些功能相关的跨膜信号传导主要由两个氨基酸序列基序介导,即免疫受体酪氨酸基激活基序(ITAMs)和免疫受体酪氨酸基抑制基序(ITIMs),它们分别作为受体与激活和抑制信号通路的接口。当ITAMs激活酪氨酸激酶及其相关分子时,ITIMs则激活相反的酪氨酸和肌醇脂质磷酸酶。在本综述中,我们将讨论目前对这些受体/基序信号传导及其有时模糊的功能界限的理解。