Regulation of the mast cell response to the type 1 Fcε receptor

被引:67
作者
Abramson, Jakub [1 ]
Pecht, Israel [1 ]
机构
[1] Weizmann Inst Sci, Dept Immunol, IL-76100 Rehovot, Israel
关键词
mast cells; immunoreceptor tyrosine-based activation motif; immunoreceptor tyrosine-based inhibitory motif; inflammatory response; cell signaling; regulation;
D O I
10.1111/j.1600-065X.2007.00518.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The type I Fc epsilon receptor (Fc epsilon RI) is one of the better understood members of its class and is central to the immunological activation of mast cells and basophils, the key players in immunoglobulin E (IgE)-dependent immediate hypersensitivity. This review provides background information on several distinct regulatory mechanisms controlling this receptor's stimulus-response coupling network. First, we review the current understanding of this network's operation, and then we focus on the inhibitory regulatory mechanisms. In particular, we discuss the different known cytosolic molecules (e.g. kinases, phosphatases, and adapters) as well as cell membrane proteins involved in negatively regulating the Fc epsilon RI-induced secretory responses. Knowledge of this field is developing at a fast rate, as new proteins endowed with regulatory functions are still being discovered. Our understanding of the complex networks by which these proteins exert regulation is limited. Although the scope of this review does not include addressing several important biochemical and biophysical aspects of the regulatory mechanisms, it does provide general insights into a central field in immunology.
引用
收藏
页码:231 / 254
页数:24
相关论文
共 241 条
[1]   Selective inhibition of the FcεRI-induced de novo synthesis of mediators by an inhibitory receptor [J].
Abramson, J ;
Licht, A ;
Pecht, I .
EMBO JOURNAL, 2006, 25 (02) :323-334
[2]   Dok protein family members are involved in signaling mediated by the type 1 Fcε receptor [J].
Abramson, J ;
Rozenblum, G ;
Pecht, I .
EUROPEAN JOURNAL OF IMMUNOLOGY, 2003, 33 (01) :85-91
[3]   Clustering the mast cell function-associated antigen (MAFA) leads to tyrosine phosphorylation of p62Dok and SHIP and affects RBL-2H3 cell cycle [J].
Abramson, J ;
Pecht, I .
IMMUNOLOGY LETTERS, 2002, 82 (1-2) :23-28
[4]  
ADACHI M, 1994, ONCOGENE, V9, P3031
[5]  
Adams S, 1998, J IMMUNOL, V161, P1853
[6]   The β subunit of the type I Fcε receptor is a target for peptides inhibiting IgE-mediated secretory response of mast cells [J].
Andrásfalvy, M ;
Péterfy, H ;
Tóth, G ;
Matkó, J ;
Abramson, J ;
Kerekes, K ;
Vámosi, G ;
Pecht, I ;
Erdei, A .
JOURNAL OF IMMUNOLOGY, 2005, 175 (05) :2801-2806
[7]  
ARM JP, 1991, J BIOL CHEM, V266, P15966
[8]  
Arm JP, 1997, J IMMUNOL, V159, P2342
[9]   Regulation of mast cell survival by IgE [J].
Asai, K ;
Kitaura, J ;
Kawakami, Y ;
Yamagata, N ;
Tsai, M ;
Carbone, DP ;
Liu, FT ;
Galli, SJ ;
Kawakami, T .
IMMUNITY, 2001, 14 (06) :791-800
[10]   The inhibitory receptor IRp60 (CD300a) is expressed and functional on human mast [J].
Bachelet, I ;
Munitz, A ;
Moretta, A ;
Moretta, L ;
Levi-Schaffer, F .
JOURNAL OF IMMUNOLOGY, 2005, 175 (12) :7989-7995