Regulation of Cys-based protein tyrosine phosphatases via reactive oxygen and nitrogen species in mast cells and basophils

被引:56
作者
Heneberg, P
Dráber, P
机构
[1] Acad Sci Czech Republ, Inst Mol Genet, Dept Signal Transduct, CZ-14220 Prague, Czech Republic
[2] Charles Univ Prague, Fac Med 3, Prague, Czech Republic
关键词
mast cell; basophils; IgE receptor; tyrosine phosphatase; hydrogen peroxide; superoxide; nitric oxide; redox-regulation;
D O I
10.2174/0929867054546636
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Activation of mast cells and basophils is accompanied by the production of reactive oxygen and nitrogen species that regulate diverse signaling pathways leading to the release of inflammatory mediators and production of a variety of cytokines. Although the functional pathways of reactive oxygen and nitrogen species in vivo are not completely understood, some novel metabolic pathways can be envisioned based on recent findings that protein tyrosine phosphatases can be regulated by reversible oxidation. In this review, we describe major sources and targets of reactive oxide and nitrogen species in mast cells and basophils. Direct and indirect regulations of class I and II Cys-based protein tyrosine phosphatases (LMW-PTP, PTEN, PTP-PEST, SHP-2, PTP1B, PTP alpha, PTP epsilon, DEP-1, TC45, SHP-1, HePTP and LAR) are discussed. The combined data highlight the role of redox-regulated protein tyrosine phosphatases as targets in the development of new ways of therapeutic intervention in allergies and inflammatory diseases.
引用
收藏
页码:1859 / 1871
页数:13
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