Blocking GSK3β-mediated dynamin1 phosphorylation enhances BDNF-dependent TrkB endocytosis and the protective effects of BDNF in neuronal and mouse models of Alzheimer's disease

Neurobiol Dis. 2015 Feb:74:377-91. doi: 10.1016/j.nbd.2014.11.020. Epub 2014 Dec 5.

Abstract

Endocytosis of tropomyosin related kinase B (TrkB) receptors has critical roles in brain-derived neurotrophic factor (BDNF) mediated signal transduction and biological function, however the mechanism that is governing TrkB endocytosis is still not completely understood. In this study, we showed that GSK3β, a key kinase in neuronal development and survival, could regulate TrkB endocytosis through phosphorylating dynamin1 (Dyn1) but not dynamin2 (Dyn2). Moreover, we found that beta-amyloid (Aβ) oligomer exposure could impair BDNF-dependent TrkB endocytosis and Akt activation through enhancing GSK3β activity in cultured hippocampal neurons, which suggested that BDNF-induced TrkB endocytosis and the subsequent signaling were impaired in neuronal model of Alzheimer's disease (AD). Notably, we found that inhibiting GSK3β phosphorylating Dyn1 by using TAT-Dyn1SpS could rescue the impaired TrkB endocytosis and Akt activation upon BDNF stimuli under Aβ exposure. Finally, TAT-Dyn1SpS could facilitate BDNF-mediated neuronal survival and cognitive enhancement in mouse models of AD. These results clarified a role of GSK3β in BDNF-dependent TrkB endocytosis and the subsequent signaling, and provided a potential new strategy by inhibiting GSK3β-induced Dyn1 phosphorylation for AD treatment.

Keywords: Alzheimer's disease; BDNF; Beta-amyloid; Dynamin1; Endocytosis; GSK3β.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / drug therapy
  • Alzheimer Disease / pathology
  • Alzheimer Disease / physiopathology*
  • Alzheimer Disease / psychology
  • Amyloid beta-Peptides / metabolism
  • Amyloid beta-Protein Precursor / genetics
  • Amyloid beta-Protein Precursor / metabolism
  • Animals
  • Brain-Derived Neurotrophic Factor / metabolism*
  • Cell Survival / drug effects
  • Cell Survival / physiology
  • Cognition / drug effects
  • Cognition / physiology
  • Disease Models, Animal
  • Dynamin I / metabolism*
  • Endocytosis / drug effects
  • Endocytosis / physiology*
  • Female
  • HEK293 Cells
  • Humans
  • Male
  • Mice, Transgenic
  • Neurons / drug effects
  • Neurons / pathology
  • Neurons / physiology*
  • Phosphorylation / drug effects
  • Presenilin-1 / genetics
  • Presenilin-1 / metabolism
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rats, Sprague-Dawley
  • Receptor, trkB / metabolism*

Substances

  • APP protein, human
  • Amyloid beta-Peptides
  • Amyloid beta-Protein Precursor
  • Brain-Derived Neurotrophic Factor
  • PSEN1 protein, human
  • Presenilin-1
  • Receptor, trkB
  • Proto-Oncogene Proteins c-akt
  • Dynamin I