Redox regulation of phosphatase function

被引:19
作者
Leslie, NR [1 ]
Lindsay, Y [1 ]
Ross, SH [1 ]
Downes, CP [1 ]
机构
[1] Univ Dundee, Sch Life Sci, Div Cell Signalling, Dundee DD1 5EH, Scotland
关键词
hydrogen peroxide; phosphatase; protein tyrosine phosphatase (PTP); reactive oxygen species (ROS); redox signalling; superoxide;
D O I
10.1042/BST0321018
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
Although reactive oxygen species play important roles in cellular physiology as signalling molecules, their molecular targets are largely unknown. A probable group of targets for mediating many of the effects of reactive oxygen species on cell signalling is the large diverse family of cysteine-dependent phosphatases, which includes the protein tyrosine phosphatases. our work and that of others suggest that the oxidative inactivation of protein and lipid phosphatases plays an important part in signalling, downstream of many cellular stimuli. Future studies should give us a clearer picture of the role of phosphatase inactivation in cellular behaviour and explain how specificity is achieved in redox signalling.
引用
收藏
页码:1018 / 1020
页数:3
相关论文
共 15 条
[1]   Redox regulation of protein tyrosine phosphatases during receptor tyrosine kinase signal transduction [J].
Chiarugi, P ;
Cirri, P .
TRENDS IN BIOCHEMICAL SCIENCES, 2003, 28 (09) :509-514
[2]   Redox regulation of PTEN and protein tyrosine phosphatases in H2O2-mediated cell signaling [J].
Cho, SH ;
Lee, CH ;
Ahn, Y ;
Kim, H ;
Kim, H ;
Ahn, CY ;
Yang, KS ;
Lee, SR .
FEBS LETTERS, 2004, 560 (1-3) :7-13
[3]   Specific and reversible inactivation of protein tyrosine phosphatases by hydrogen peroxide: Evidence for a sulfenic acid intermediate and implications for redox regulation [J].
Denu, JM ;
Tanner, KG .
BIOCHEMISTRY, 1998, 37 (16) :5633-5642
[4]   Free radicals in the physiological control of cell function [J].
Dröge, W .
PHYSIOLOGICAL REVIEWS, 2002, 82 (01) :47-95
[5]   Redox-dependent signal transduction [J].
Finkel, T .
FEBS LETTERS, 2000, 476 (1-2) :52-54
[6]   Calcium-dependent oxidation of thioredoxin during cellular growth initiation [J].
Gitler, C ;
Zarmi, B ;
Kalef, E ;
Meller, R ;
Zor, U ;
Goldman, R .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 290 (02) :624-628
[7]   Reversible inactivation of the tumor suppressor PTEN by H2O2 [J].
Lee, SR ;
Yang, KS ;
Kwon, J ;
Lee, C ;
Jeong, W ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (23) :20336-20342
[8]   Reversible inactivation of protein-tyrosine phosphatase 1B in A431 cells stimulated with epidermal growth factor [J].
Lee, SR ;
Kwon, KS ;
Kim, SR ;
Rhee, SG .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (25) :15366-15372
[9]   Redox regulation of PI 3-kinase signalling via inactivation of PTEN [J].
Leslie, NR ;
Bennett, D ;
Lindsay, YE ;
Stewart, H ;
Gray, A ;
Downes, CP .
EMBO JOURNAL, 2003, 22 (20) :5501-5510
[10]   PTEN: The down side of PI 3-kinase signalling [J].
Leslie, NR ;
Downes, CP .
CELLULAR SIGNALLING, 2002, 14 (04) :285-295