GSK-3 and Wnt signaling in neurogenesis and bipolar disorder

被引:174
|
作者
Valvezan, Alexander J. [1 ,2 ]
Klein, Peter S. [1 ,2 ]
机构
[1] Univ Penn, Sch Med, Cell & Mol Biol Grad Grp, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Dept Med, Div Hematol Oncol, Philadelphia, PA 19104 USA
来源
关键词
Wnt; GSK-3; neurogenesis; lithium; bipolar disorder; behavior; development; psychiatric; GLYCOGEN-SYNTHASE KINASE-3; ADULT HIPPOCAMPAL NEUROGENESIS; INHIBITORY SERINE-PHOSPHORYLATION; HYPOXIA-INDUCIBLE FACTOR-1-ALPHA; BETA-CATENIN; DENTATE GYRUS; NERVOUS-SYSTEM; NEURONAL DIFFERENTIATION; TARGETED DISRUPTION; MOLECULAR-MECHANISM;
D O I
10.3389/fnmol.2012.00001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The canonical Wnt signaling pathway is critical for development of the mammalian central nervous system and regulates diverse processes throughout adulthood, including adult neurogenesis. Glycogen synthase kinase-3 (GSK-3) antagonizes the canonical Wnt pathway and therefore also plays a central role in neural development and adult neurogenesis. Lithium, the first line of therapy for bipolar disorder, inhibits GSK-3, activates Wnt signaling and stimulates adult neurogenesis, which may be important for its therapeutic effects. GSK-3 also regulates other critical signaling pathways which may contribute to the therapeutic effects of lithium, including growth factor/neurotrophin signaling downstream of Akt. Here we will review the roles of GSK-3 in CNS development and adult neurogenesis, with a focus on the canonical Wnt pathway. We will also discuss the validation of GSK-3 as the relevant target of lithium and the mechanisms downstream of GSK-3 that influence mammalian behavior.
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页数:13
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