Targeting GSK3 signaling as a potential therapy of neurodegenerative diseases and aging

被引:99
作者
Duda, Przemyslaw [1 ]
Wisniewski, Janusz [1 ]
Wojtowicz, Tomasz [1 ]
Wojcicka, Olga [1 ]
Jaskiewicz, Michal [1 ]
Drulis-Fajdasz, Dominika [1 ]
Rakus, Dariusz [1 ]
McCubrey, James A. [2 ]
Gizak, Agnieszka [1 ]
机构
[1] Univ Wroclaw, Dept Mol Physiol & Neurobiol, Wroclaw, Poland
[2] East Carolina Univ, Brody Sch Med, Dept Microbiol & Immunol, Greenville, NC 27858 USA
关键词
Synaptic plasticity; brain aging; inflammation; Alzheimer's disease; Parkinson's disease; schizophrenia; astrocytes; GLYCOGEN-SYNTHASE KINASE-3; LONG-TERM POTENTIATION; ALZHEIMERS-DISEASE; PREFRONTAL CORTEX; ALPHA-SYNUCLEIN; PROTEIN-KINASE; SYNAPTIC-TRANSMISSION; COGNITIVE IMPAIRMENT; TAU PHOSPHORYLATION; PARKINSONS-DISEASE;
D O I
10.1080/14728222.2018.1526925
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Glycogen synthase kinase 3 (GSK3) is at the center of cellular signaling and controls various aspects of brain functions, including development of the nervous system, neuronal plasticity and onset of neurodegenerative disorders. Areas covered: In this review, recent efforts in elucidating the roles of GSK3 in neuronal plasticity and development of brain pathologies; Alzheimer's and Parkinson's disease, schizophrenia, and age-related neurodegeneration are described. The effect of microglia and astrocytes on development of the pathological states is also discussed. Expert opinion: GSK3 and its signaling pathway partners hold great promise as therapeutic target(s) for a multitude of neurological disorders. Activity of the kinase is often elevated in brain disorders. However, due to the wide range of GSK3 cellular targets, global inhibition of the kinase leads to severe side-effects and GSK3 inhibitors rarely reach Phase-2 clinical trials. Thus, a selective modulation of a specific cellular pool of GSK3 or specific down- or upstream partners of the kinase might provide more efficient anti-neurodegenerative therapies.
引用
收藏
页码:833 / 848
页数:16
相关论文
共 177 条
[91]   Regulation of mouse brain glycogen synthase kinase-3 by atypical antipsychotics [J].
Li, Xiaohua ;
Rosborough, Kelley M. ;
Friedman, Ari B. ;
Zhu, Wawa ;
Roth, Kevin A. .
INTERNATIONAL JOURNAL OF NEUROPSYCHOPHARMACOLOGY, 2007, 10 (01) :7-19
[92]   Disruption of Akt signaling decreases dopamine sensitivity in modulation of inhibitory synaptic transmission in rat prefrontal cortex [J].
Li, Yan-Chun ;
Yang, Sha-Sha ;
Gao, Wen-Jun .
NEUROPHARMACOLOGY, 2016, 108 :403-414
[93]   A unique type of GSK-3 inhibitor brings new opportunities to the clinic [J].
Licht-Murava, Avital ;
Paz, Rom ;
Vaks, Lilach ;
Avrahami, Limor ;
Plotkin, Batya ;
Eisenstein, Miriam ;
Eldar-Finkelman, Hagit .
SCIENCE SIGNALING, 2016, 9 (454)
[94]   The role of inflammatory mediators in the biology of major depression: central nervous system cytokines modulate the biological substrate of depressive symptoms, regulate stress-responsive systems, and contribute to neurotoxicity and neuroprotection [J].
Licinio, J ;
Wong, ML .
MOLECULAR PSYCHIATRY, 1999, 4 (04) :317-327
[95]   Bromocriptine activates NQO1 via Nrf2-PI3K/Akt signaling: Novel cytoprotective mechanism against oxidative damage [J].
Lim, Ju Hee ;
Kim, Kyeong-Man ;
Kim, Seong Who ;
Hwang, Onyou ;
Choi, Hyun Jin .
PHARMACOLOGICAL RESEARCH, 2008, 57 (05) :325-331
[96]   Glycogen synthase kinase-3β phosphorylates bax and promotes its mitochondrial localization during neuronal apoptosis [J].
Linseman, DA ;
Butts, BD ;
Precht, TA ;
Phelps, RA ;
Le, SS ;
Laessig, TA ;
Bouchard, RJ ;
Florez-McClure, ML ;
Heidenreich, KA .
JOURNAL OF NEUROSCIENCE, 2004, 24 (44) :9993-10002
[97]   Neurobehavioural evaluation of resveratrol in murine models of anxiety and schizophrenia [J].
Magaji, Mohammed Garba ;
Iniaghe, Loretta Oghenekome ;
Abolarin, Mutiat ;
Abdullahi, Opeyemi Isa ;
Magaji, Rabiu Abdusalam .
METABOLIC BRAIN DISEASE, 2017, 32 (02) :437-442
[98]   AKT/PKB Signaling: Navigating the Network [J].
Manning, Brendan D. ;
Toker, Alex .
CELL, 2017, 169 (03) :381-405
[99]   Evidence for Irreversible Inhibition of Glycogen Synthase Kinase-3β by Tideglusib [J].
Manuel Dominguez, Juan ;
Fuertes, Ana ;
Orozco, Leyre ;
del Monte-Millan, Maria ;
Delgado, Elena ;
Medina, Miguel .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (02) :893-904
[100]   Disrupted in Schizophrenia 1 Regulates Neuronal Progenitor Proliferation via Modulation of GSK3β/β-Catenin Signaling [J].
Mao, Yingwei ;
Ge, Xuecai ;
Frank, Christopher L. ;
Madison, Jon M. ;
Koehler, Angela N. ;
Doud, Mary Kathryn ;
Tassa, Carlos ;
Berry, Erin M. ;
Soda, Takahiro ;
Singh, Karun K. ;
Biechele, Travis ;
Petryshen, Tracey L. ;
Moon, Randall T. ;
Haggarty, Stephen J. ;
Tsai, Li-Huei .
CELL, 2009, 136 (06) :1017-1031