Protein tyrosine phosphatases in health and disease

被引:127
作者
Hendriks, Wiljan J. A. J. [1 ]
Elson, Ari [2 ]
Harroch, Sheila [3 ]
Pulido, Rafael [4 ]
Stoker, Andrew [5 ]
den Hertog, Jeroen [6 ,7 ,8 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, NL-6525 ED Nijmegen, Netherlands
[2] Weizmann Inst Sci, Dept Mol Genet, IL-76100 Rehovot, Israel
[3] Inst Pasteur, Dept Neurosci, Paris, France
[4] Ctr Invest Principe Felipe, Valencia, Spain
[5] UCL, Inst Child Hlth, Neural Dev Unit, London WC1E 6BT, England
[6] KNAW, Hubrecht Inst, NL-3584 CT Utrecht, Netherlands
[7] Univ Med Ctr Utrecht, Utrecht, Netherlands
[8] Leiden Univ, Inst Biol Leiden, NL-2300 RA Leiden, Netherlands
关键词
bone morphogenesis; hereditary disease; neuronal development; post-translational modification; protein tyrosine phosphatase; synaptogenesis; NF-KAPPA-B; MAP KINASE PHOSPHATASES; SRC-FAMILY KINASES; RECEPTOR-TYPE-Z; SYNAPSE FORMATION; PTP-SIGMA; AMPA RECEPTOR; OSTEOCLAST FUNCTION; GENE-EXPRESSION; CELL;
D O I
10.1111/febs.12000
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
Protein tyrosine phosphatases (PTPs) represent a super-family of enzymes that play essential roles in normal development and physiology. In this review, we will discuss the PTPs that have a causative role in hereditary diseases in humans. In addition, recent progress in the development and analysis of animal models expressing mutant PTPs will be presented. The impact of PTP signaling on health and disease will be exemplified for the fields of bone development, synaptogenesis and central nervous system diseases. Collectively, research on PTPs since the late 1980's yielded the cogent view that development of PTP-directed therapeutic tools is essential to further combat human disease.
引用
收藏
页码:708 / 730
页数:23
相关论文
共 160 条
[11]   Development of severe skeletal defects in induced SHP-2-deficient adult mice: a model of skeletal malformation in humans with SHP-2 mutations [J].
Bauler, Timothy J. ;
Kamiya, Nobuhiro ;
Lapinski, Philip E. ;
Langewisch, Eric ;
Mishina, Yuji ;
Wilkinson, John E. ;
Feng, Gen-Sheng ;
King, Philip D. .
DISEASE MODELS & MECHANISMS, 2011, 4 (02) :228-U112
[12]   The FERM and PDZ Domain-Containing Protein Tyrosine Phosphatases, PTPN4 and PTPN3, Are Both Dispensable for T Cell Receptor Signal Transduction [J].
Bauler, Timothy J. ;
Hendriks, Wiljan J. A. J. ;
King, Philip D. .
PLOS ONE, 2008, 3 (12)
[13]  
Baum Matthew L, 2010, Commun Integr Biol, V3, P419, DOI 10.4161/cib.3.5.12692
[14]   The dual-specificity MAP kinase phosphatases: critical roles in development and cancer [J].
Bermudez, O. ;
Pages, G. ;
Gimond, C. .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2010, 299 (02) :C189-C202
[15]   Fyn and PTP-PEST-mediated regulation of Wiskott-Aldrich syndrome protein (WASp) tyrosine phosphorylation is required for coupling T cell antigen receptor engagement to WASp effector function and T cell activation [J].
Bodour, K ;
Zhang, JY ;
Shi, F ;
Leng, S ;
Collins, M ;
Siminovitch, KA .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 199 (01) :99-111
[16]  
Bouyain Samuel, 2010, Commun Integr Biol, V3, P284
[17]   The protein tyrosine phosphatases PTPRZ and PTPRG bind to distinct members of the contactin family of neural recognition molecules [J].
Bouyain, Samuel ;
Watkins, Dara J. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (06) :2443-2448
[18]   Osteoclast differentiation and activation [J].
Boyle, WJ ;
Simonet, WS ;
Lacey, DL .
NATURE, 2003, 423 (6937) :337-342
[19]   Synaptic plasticity: one STEP at a time [J].
Braithwaite, Steven P. ;
Paul, Surojit ;
Nairn, Angus C. ;
Lombroso, Paul J. .
TRENDS IN NEUROSCIENCES, 2006, 29 (08) :452-458
[20]   Cadherin-catenin adhesion complexes at the synapse [J].
Brigidi, G. Stefano ;
Bamji, Shernaz X. .
CURRENT OPINION IN NEUROBIOLOGY, 2011, 21 (02) :208-214