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.
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Authors | Noriko Hattori, Hiroshi Nomoto, Hidefumi Fukumitsu, Satoshi Mishima, Shoei Furukawa |
Journal | Biomedical research (Tokyo, Japan)
(Biomed Res)
Vol. 28
Issue 6
Pg. 295-9
(Dec 2007)
ISSN: 1880-313X [Electronic] Japan |
PMID | 18202519
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- AMP N1-oxide
- STAT3 Transcription Factor
- Stat3 protein, rat
- Adenosine Monophosphate
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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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