Of ITIMs, ITAMs, and ITAMis: revisiting immunoglobulin Fc receptor signaling

被引:114
作者
Getahun, Andrew [1 ]
Cambier, John C. [1 ]
机构
[1] Univ Colorado, Sch Med, Dept Immunol & Microbiol, Aurora, CO 80045 USA
关键词
Fc receptors; signal transduction; ITAMs; ITIMs; SHIP; SHP; TYROSINE-PHOSPHATASE SHP-1; AFFINITY IGE RECEPTOR; B-CELL ACTIVATION; 5-PHOSPHATASE SHIP BINDS; GAMMA-RIIB; NEGATIVE REGULATION; EPSILON-RI; ANTIINFLAMMATORY ACTIVITY; MEDIATED INHIBITION; CRYSTAL-STRUCTURE;
D O I
10.1111/imr.12336
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:66 / 73
页数:8
相关论文
共 88 条
[1]   IgG1 and IVIg induce inhibitory ITAM signaling through FcγRIII controlling inflammatory responses [J].
Aloulou, Meryem ;
Ben Mkaddem, Sanae ;
Biarnes-Pelicot, Martine ;
Boussetta, Tarek ;
Souchet, Herve ;
Rossato, Elisabetta ;
Benhamou, Marc ;
Crestani, Bruno ;
Zhu, Zhou ;
Blank, Ulrich ;
Launay, Pierre ;
Monteiro, Renato C. .
BLOOD, 2012, 119 (13) :3084-3096
[2]   Intravenous gammaglobulin suppresses inflammation through a novel TH2 pathway [J].
Anthony, Robert M. ;
Kobayashi, Toshihiko ;
Wermeling, Fredrik ;
Ravetch, Jeffrey V. .
NATURE, 2011, 475 (7354) :110-U133
[3]   Shifting FcγRIIA-ITAM from activation to inhibitory configuration ameliorates arthritis [J].
Ben Mkaddem, Sanae ;
Hayem, Gilles ;
Joensson, Friederike ;
Rossato, Elisabetta ;
Boedec, Erwan ;
Boussetta, Tarek ;
El Benna, Jamel ;
Launay, Pierre ;
Goujon, Jean-Michel ;
Benhamou, Marc ;
Bruhns, Pierre ;
Monteiro, Renato C. .
JOURNAL OF CLINICAL INVESTIGATION, 2014, 124 (09) :3945-3959
[4]  
Blery M, 1997, J BIOL CHEM, V272, P8989
[5]   SHIP modulates immune receptor responses by regulating membrane association of Btk [J].
Bolland, S ;
Pearse, RN ;
Kurosaki, T ;
Ravetch, JV .
IMMUNITY, 1998, 8 (04) :509-516
[6]   Partially distinct molecular mechanisms mediate inhibitory FcγRIIB signaling in resting and activated B cells' [J].
Brauweiler, A ;
Tamir, I ;
Marschner, S ;
Helgason, CD ;
Cambier, JC .
JOURNAL OF IMMUNOLOGY, 2001, 167 (01) :204-211
[7]   Autonomous SHIP-dependent FcγR signaling in pre-B cells leads to inhibition of cell migration and induction of cell death [J].
Brauweiler, AM ;
Cambier, JC .
IMMUNOLOGY LETTERS, 2004, 92 (1-2) :75-81
[8]   Cutting edge: Acute and chronic exposure of immature B cells to antigen leads to impaired homing and SHIP1-dependent reduction in stromal cell-derived factor-1 responsiveness [J].
Brauweiler, Anne ;
Merrell, Kevin ;
Gauld, Stephen B. ;
Cambier, John C. .
JOURNAL OF IMMUNOLOGY, 2007, 178 (06) :3353-3357
[9]   Molecular basis of the recruitment of the SH2 domain-containing inositol 5-phosphatases SHIP1 and SHIP2 by FcγRIIB [J].
Bruhns, P ;
Vély, F ;
Malbec, O ;
Fridman, WH ;
Vivier, E ;
Daëron, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (48) :37357-37364
[10]   Regulation of hematopoietic cell function by inhibitory immunoglobulin G receptors and their inositol lipid phosphatase effectors [J].
Cady, Carol T. ;
Rice, Jeffrey S. ;
Ott, Vanessa L. ;
Cambier, John C. .
IMMUNOLOGICAL REVIEWS, 2008, 224 :44-57