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AMP N1-oxide potentiates astrogenesis by cultured neural stem/progenitor cells through STAT3 activation.

Abstract
We earlier identified adenosine monophosphate (AMP) N1-oxide as a unique compound of royal jelly (RJ) that induces neurite outgrowth from cultured rat pheochromocytoma PC12 cells. In the present study, the effects of AMP N1-oxide on the proliferation and/or differentiation of cultured neural stem/progenitor cells (NSCs) were examined. As for cell proliferation, low micromolar concentrations of AMP N1-oxide or its parent compound, AMP, similarly enhanced the NSC proliferation-inducing activity of basic fibroblast growth factor (FGF-2), although neither compound tested alone affected cell proliferation. Conversely, high concentrations of AMP N1-oxide (over 20 microM) markedly suppressed cell growth even in the presence of FGF-2. However, this suppression was not observed with AMP. As for cell differentiation, AMP N1-oxide, but not AMP, increased the generation of astrocytes in a dose-dependent manner when the cells were cultured in medium lacking FGF-2. The generation of neurons or oligodendrocytes was not influenced by AMP N1-oxide. Furthermore, AMP N1-oxide increased the phosphorylation of STAT3 (signal transducer and activator of transcription 3), a transcription factor that mediates the expression of astrocytespecific genes. These results suggest that AMP N1-oxide is one of the components that facilitates astrogenesis by NSCs through activation of STAT3.
AuthorsNoriko Hattori, Hiroshi Nomoto, Hidefumi Fukumitsu, Satoshi Mishima, Shoei Furukawa
JournalBiomedical research (Tokyo, Japan) (Biomed Res) Vol. 28 Issue 6 Pg. 295-9 (Dec 2007) ISSN: 1880-313X [Electronic] Japan
PMID18202519 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • AMP N1-oxide
  • STAT3 Transcription Factor
  • Stat3 protein, rat
  • Adenosine Monophosphate
Topics
  • Adenosine Monophosphate (analogs & derivatives, pharmacology, physiology)
  • Animals
  • Astrocytes (cytology, drug effects, metabolism)
  • Cell Differentiation
  • Cell Proliferation
  • Cells, Cultured
  • Neurites (drug effects, metabolism)
  • Neurons (cytology, drug effects, metabolism)
  • Rats
  • STAT3 Transcription Factor (metabolism)
  • Signal Transduction
  • Stem Cells (cytology, drug effects, metabolism)

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