N-cadherin mediates nitric oxide-induced neurogenesis in young and retired breeder neurospheres

Neuroscience. 2006 Jun 30;140(2):377-88. doi: 10.1016/j.neuroscience.2006.02.064. Epub 2006 Apr 3.

Abstract

Neurogenesis may contribute to functional recovery after neural injury. Nitric oxide donors such as DETA-NONOate promote functional recovery after stroke. However, the mechanisms underlying functional improvement have not been ascertained. We therefore investigated the effects of DETA-NONOate on neural progenitor/stem cell neurospheres derived from the subventricular zone from young and retired breeder rat brain. Subventricular zone cells were dissociated from normal young adult male Wistar rats (2-3 months old) and retired breeder rats (14 months old), treated with or without DETA-NONOate. Subventricular zone neurosphere formation, proliferation, telomerase activity, and Neurogenin 1 mRNA expression were significantly decreased and glial fibrillary acidic protein expression was significantly increased in subventricular zone neurospheres from retired breeder rats compared with young rats. Treatment of neurospheres with DETA-NONOate significantly decreased neurosphere formation and telomerase activity, and promoted neuronal differentiation and neurite outgrowth concomitantly with increased N-cadherin and beta-catenin mRNA expression in both young and old neurospheres. DETA-NONOate selectively increased Neurogenin 1 and decreased glial fibrillary acidic protein mRNA expression in retired breeder neurospheres. N-cadherin significantly increased Neurogenin 1 mRNA expression in young and old neurospheres. Anti-N-cadherin reversed DETA-NONOate-induced neurosphere adhesion, neuronal differentiation, neurite outgrowth, and beta-catenin mRNA expression. Our data indicate that age has a potent effect on the characteristics of subventricular zone neurospheres; neurospheres from young rats show significantly higher formation, proliferation and telomerase activity than older neurospheres. In contrast, older neurospheres exhibit significantly increased glial differentiation than young neurospheres. DETA-NONOate promotes neuronal differentiation and neurite outgrowth in both young and older neurospheres. The molecular mechanisms associated with the DETA-NONOate modulation of neurospheres from young and older animals as well age dependent effects of neurospheres appear to be controlled by N-cadherin and beta-catenin gene expression, which subsequently regulates the neuronal differentiating factor Neurogenin expression in both young and old neural progenitor cells.

Publication types

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

MeSH terms

  • Aging / physiology
  • Animals
  • Antibodies / pharmacology
  • Basic Helix-Loop-Helix Transcription Factors / genetics
  • Brain / cytology
  • Brain / growth & development*
  • Brain / metabolism
  • Cadherins / metabolism*
  • Cell Culture Techniques / methods
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology*
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Glial Fibrillary Acidic Protein / genetics
  • Male
  • Nerve Tissue Proteins / genetics
  • Neurites / drug effects
  • Neurites / metabolism
  • Neurons / drug effects
  • Neurons / metabolism*
  • Nitric Oxide / metabolism*
  • Nitric Oxide Donors / pharmacology
  • Nitroso Compounds / pharmacology
  • RNA, Messenger / drug effects
  • RNA, Messenger / metabolism
  • Rats
  • Rats, Wistar
  • Spheroids, Cellular
  • Stem Cells / drug effects
  • Stem Cells / metabolism*
  • Telomerase / metabolism
  • beta Catenin / genetics

Substances

  • Antibodies
  • Basic Helix-Loop-Helix Transcription Factors
  • Cadherins
  • Glial Fibrillary Acidic Protein
  • Nerve Tissue Proteins
  • Nitric Oxide Donors
  • Nitroso Compounds
  • RNA, Messenger
  • beta Catenin
  • 2,2'-(hydroxynitrosohydrazono)bis-ethanamine
  • Neurog1 protein, mouse
  • Nitric Oxide
  • Telomerase