4.6 Article

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

期刊

MOLECULAR NEUROBIOLOGY
卷 55, 期 8, 页码 6500-6517

出版社

SPRINGER
DOI: 10.1007/s12035-017-0860-4

关键词

Adult neurogenesis; Neural stem cells; Radial glia-like cells; Parkinson's disease

资金

  1. Council of Scientific and Industrial Research (CSIR) Network grant miND [BSC0115]
  2. CSIR-Central Drug Research Institute (CDRI), Lucknow, India
  3. Indian Council of Medical Research (ICMR), New Delhi, India
  4. CSIR, New Delhi, India

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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.

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