[When we have learned about the brain development from a disease-oriented study: DBZ regulates cortical cell positioning and neurite extension by sustaining the anterograde transport of Lis1/DISC1 through control of Ndel1 phosphorylation]

Nihon Shinkei Seishin Yakurigaku Zasshi. 2016 Apr;36(2):43-50.
[Article in Japanese]

Abstract

Cell positioning and neuronal network formation are crucial for proper brain function. Disrupted-In-Schizophrenia 1 (DISC1) is anterogradely transported to the neurite tips, together with Lis1, and functions in neurite extension via suppression of GSK3β activity. Then, transported Lis1 is retrogradely transported and functions in cell migration. Here, we show that DISC1-binding zinc finger protein (DBZ) regulates mouse cortical cell positioning and neurite development in vivo, together with DISC1. DBZ hindered Ndel1 phosphorylation at threonine 219 and serine 251. DBZ depletion or expression of a double-phosphorylated mimetic form of Ndel1 impaired the transport of Lis1 and DISC1 to the neurite tips and hampered microtubule elongation. Moreover, application of DISC1 or a GSK3β inhibitor rescued the impairments caused by DBZ insufficiency or double-phosphorylated Ndel1 expression. We concluded that DBZ controls cell positioning and neurite development by interfering with Ndel1 from disproportionate phosphorylation, which is critical for appropriate anterograde transport of the DISC1-complex.

Publication types

  • Review

MeSH terms

  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / metabolism*
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / physiology
  • Animals
  • Biological Transport / genetics
  • Carrier Proteins / metabolism*
  • Cerebral Cortex / cytology*
  • Cerebral Cortex / growth & development*
  • Cerebral Cortex / pathology
  • DNA-Binding Proteins / physiology*
  • Glycogen Synthase Kinase 3 / antagonists & inhibitors
  • Glycogen Synthase Kinase 3 / physiology
  • Glycogen Synthase Kinase 3 beta
  • Humans
  • Mice
  • Microtubule-Associated Proteins / metabolism*
  • Microtubule-Associated Proteins / physiology
  • Nerve Tissue Proteins / metabolism*
  • Nerve Tissue Proteins / physiology
  • Neurites / pathology
  • Neurites / physiology*
  • Neurons / pathology*
  • Phosphorylation / genetics
  • Schizophrenia / genetics
  • Schizophrenia / pathology
  • Transcription Factors / physiology*

Substances

  • Carrier Proteins
  • DISC1 protein, human
  • DNA-Binding Proteins
  • Microtubule-Associated Proteins
  • NDEL1 protein, human
  • Nerve Tissue Proteins
  • Transcription Factors
  • ZNF365 protein, human
  • GSK3B protein, human
  • Glycogen Synthase Kinase 3 beta
  • Gsk3b protein, mouse
  • Glycogen Synthase Kinase 3
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase
  • PAFAH1B1 protein, human