Early involvement of synapsin III in neural progenitor cell development in the adult hippocampus

J Comp Neurol. 2008 Apr 20;507(6):1860-70. doi: 10.1002/cne.21643.

Abstract

Synapsin III is a synaptic vesicle-associated protein that is expressed in cells of the subgranular layer of the hippocampal dentate gyrus, a brain region known to sustain substantial levels of neurogenesis into adulthood. Here we tested the hypothesis that synapsin III plays a role in adult neurogenesis with synapsin III knockout and wild-type mice. Immunocytochemistry of the adult hippocampal dentate gyrus revealed that synapsin III colocalizes with markers of neural progenitor cell development (nestin, PSA-NCAM, NeuN, and Tuj1) but did not colocalize with markers of mitosis (Ki67 and PCNA). Because neurogenesis consists of a number of stages, the proliferation, survival, and differentiation of neural progenitor cells were systematically quantitated in the hippocampal dentate gyrus of adult synapsin III knockout and wild-type mice. We found a 30% decrease in proliferation and a 55% increase in survival of neural progenitor cells in synapsin III knockout mice. We also observed a 6% increase in the number of neural progenitor cells that differentiated into neurons. No difference in the volume of the dentate gyrus was observed between synapsin III knockout and wild-type mice. Collectively, our results demonstrate a novel role for synapsin III in regulating the proliferation of neural progenitor cells in the adult hippocampal dentate gyrus. These findings suggest a distinct function for this synaptic vesicle protein, in addition to its role in neurotransmission.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Age Factors
  • Animals
  • Biomarkers / metabolism
  • Cell Differentiation / physiology*
  • Cell Proliferation
  • Cell Survival / physiology
  • DNA-Binding Proteins
  • Dentate Gyrus / cytology
  • Dentate Gyrus / metabolism*
  • Female
  • Fluorescent Antibody Technique
  • Intermediate Filament Proteins / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nerve Growth Factors / genetics
  • Nerve Tissue Proteins / metabolism
  • Nestin
  • Neural Cell Adhesion Molecule L1 / metabolism
  • Neuronal Plasticity / physiology
  • Neurons / cytology
  • Neurons / metabolism*
  • Nuclear Proteins / metabolism
  • Sialic Acids / metabolism
  • Stem Cells / cytology
  • Stem Cells / metabolism*
  • Synapsins / genetics*
  • Time Factors
  • Tubulin / metabolism

Substances

  • Biomarkers
  • DNA-Binding Proteins
  • Intermediate Filament Proteins
  • Nerve Growth Factors
  • Nerve Tissue Proteins
  • Nes protein, mouse
  • Nestin
  • NeuN protein, mouse
  • Neural Cell Adhesion Molecule L1
  • Nuclear Proteins
  • Sialic Acids
  • Synapsins
  • Tubulin
  • beta3 tubulin, mouse
  • polysialyl neural cell adhesion molecule