Regulation of c-fos and c-jun gene expression by lipopolysaccharide and cytokines in primary cultured astrocytes: effect of PKA and PKC pathways

The effects of lipopolysaccharide (LPS) and several cytokines on the c-fos and c-jun mRNA expression were examined in primary cultured astrocytes. Either LPS (500 ng/mL) or interferon-γ (IFN-γ; 5 ng/mL) alone increased the level of c-fos mRNA (1 h). However, tumor necrosis factor-α (TNF-α; 10 ng/mL)...

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Veröffentlicht in:Archives of pharmacal research 2004, 27(4), , pp.396-401
Hauptverfasser: Suh, Hong-Won, Choi, Seong-Soo, Lee, Jin-Koo, Lee, Han-Kyu, Han, Eun-Jung, Lee, Jongho
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Sprache:eng
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Zusammenfassung:The effects of lipopolysaccharide (LPS) and several cytokines on the c-fos and c-jun mRNA expression were examined in primary cultured astrocytes. Either LPS (500 ng/mL) or interferon-γ (IFN-γ; 5 ng/mL) alone increased the level of c-fos mRNA (1 h). However, tumor necrosis factor-α (TNF-α; 10 ng/mL) or interleukin-1β (IL-1β; 5 ng/mL) alone showed no significant induction of the level of c-fos mRNA. TNF-α showed a potentiating effect in the regulation of LPS-induced c-fos mRNA expression, whereas LPS showed an inhibitory action against IFN-γ-inducedc-fos mRNA expression. LPS, but not TNF-α, IL-β and IFN-γ, increased the level of c-jun mRNA (1 h). TNF-α and IFN-γ showed an inhibitory action against LPS-induced c-jun mRNA expression. Both phorbol 12-myristate 13-acetate (PMA; 2.5 mM) and forskolin (FSK; 5 mM) increased the c-fos and c-jun mRNA expressions. In addition, the level of c-fos mRNA was expressed in an antagonistic manner when LPS was combined with PMA. When LPS was co-treated with either PMA or FSK, it showed an additive interaction for the induction of c-jun mRNA expression. Our results suggest that LPS and cytokines may be actively involved in the regulation of c-fos andc-jun mRNA expressions in primary cultured astrocytes. Moreover, both the PKA and PKC pathways may regulate the LPS-induced c-fos and c-jun mRNA expressions in different ways.
ISSN:0253-6269
1976-3786
DOI:10.1007/bf02980080