Glycogen Synthase Kinase-3β Regulates Equilibrium Between Neurogenesis and Gliogenesis in Rat Model of Parkinson's Disease: a Crosstalk with Wnt and Notch Signaling

被引:55
作者
Singh, Sonu [1 ]
Mishra, Akanksha [1 ,2 ]
Bharti, Sachi [1 ]
Tiwari, Virendra [1 ]
Singh, Jitendra [1 ]
Parul [1 ]
Shukla, Shubha [1 ,2 ]
机构
[1] CSIR, Cent Drug Res Inst, Div Pharmacol, Sect 10, Sitapur Rd, Lucknow 226031, Uttar Pradesh, India
[2] Acad Sci & Innovat Res, New Delhi, India
关键词
Adult neurogenesis; Neural stem cells; Radial glia-like cells; Parkinson's disease; NEURAL STEM-CELLS; NEURONS; PHOSPHORYLATION; PROLIFERATION; ACTIVATION; STRESS; CYCLE; PROGENITORS; NEUROBLASTS; DEPLETION;
D O I
10.1007/s12035-017-0860-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurogenesis involves generation of functional newborn neurons from neural stem cells (NSCs). Insufficient formation or accelerated degeneration of newborn neurons may contribute to the severity of motor/nonmotor symptoms of Parkinson's disease (PD). However, the functional role of adult neurogenesis in PD is yet not explored and whether glycogen synthase kinase-3 beta (GSK-3 beta) affects multiple steps of adult neurogenesis in PD is still unknown. We investigated the possible underlying molecular mechanism of impaired adult neurogenesis associated with PD. Herein, we show that single intra-medial forebrain bundle (MFB) injection of 6-hydroxydopamine (6-OHDA) efficiently induced long-term activation of GSK-3 beta and reduced NSC self-renewal, proliferation, neuronal migration, and neuronal differentiation accompanied with increased astrogenesis in subventricular zone (SVZ) and hippocampal dentate gyrus (DG). Indeed, 6-OHDA also delayed maturation of neuroblasts in the DG as witnessed by their reduced dendritic length and arborization. Using a pharmacological approach to inhibit GSK-3 beta activation by specific inhibitor SB216763, we show that GSK-3 beta inhibition enhances radial glial cells, NSC proliferation, self-renewal in the SVZ, and the subgranular zone (SGZ) in the rat PD model. Pharmacological inhibition of GSK-3 beta activity enhances neuroblast population in SVZ and SGZ and promotes migration of neuroblasts towards the rostral migratory stream and lesioned striatum from dorsal SVZ and lateral SVZ, respectively, in PD model. GSK-3 beta inhibition enhances dendritic arborization and survival of granular neurons and stimulates NSC differentiation towards the neuronal phenotype in DG of PD model. The aforementioned effects of GSK-3 beta involve a crosstalk between Wnt/beta-catenin and Notch signaling pathways that are known to regulate NSC dynamics.
引用
收藏
页码:6500 / 6517
页数:18
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