Ciliary neurotrophic factor (CNTF) plus soluble CNTF receptor alpha increases cyclooxygenase-2 expression, PGE2 release and interferon-gamma-induced CD40 in murine microglia

J Neuroinflammation. 2009 Mar 6:6:7. doi: 10.1186/1742-2094-6-7.

Abstract

Background: Ciliary neurotrophic factor (CNTF) has been regarded as a potent trophic factor for motor neurons. However, recent studies have shown that CNTF exerts effects on glial cells as well as neurons. For instance, CNTF stimulates astrocytes to secrete FGF-2 and rat microglia to secrete glial cell line-derived neurotrophic factor (GDNF), which suggest that CNTF exerts effects on astrocytes and microglia to promote motor neuron survival indirectly. As CNTF is structurally related to IL-6, which can stimulate immune functions of microglia, we hypothesized that CNTF might exert similar effects.

Methods: We performed 2-D and 1-D proteomic experiments with western blotting and flow cytometry to examine effects of CNTF on primary microglia derived from neonatal mouse brains.

Results: We show that murine microglia express CNTF receptor alpha (CNTFRalpha), which can be induced by interferon-gamma (IFNgamma). Whereas IL-6 activated STAT-3 and ERK phosphorylation, CNTF did not activate these pathways, nor did CNTF increase p38 MAP kinase phosphorylation. Using 2-D western blot analysis, we demonstrate that CNTF induced the dephosphorylation of a set of proteins and phosphorylation of a different set. Two proteins that were phosphorylated upon CNTF treatment were the LYN substrate-1 and beta-tubulin 5. CNTF weakly stimulated microglia, whereas a stronger response was obtained by adding exogenous soluble CNTFRalpha (sCNTFRalpha) as has been observed for IL-6. When used in combination, CNTF and sCNTFRalpha collaborated with IFNgamma to increase microglial surface expression of CD40 and this effect was quite pronounced when the microglia were differentiated towards dendritic-like cells. CNTF/sCNTFRalpha complex, however, failed to increase MHC class II expression beyond that induced by IFNgamma. The combination of CNTF and sCNTFRalpha, but not CNTF alone, enhanced microglial Cox-2 protein expression and PGE2 secretion (although CNTF was 30 times less potent than LPS). Surprisingly, Cox-2 production was enhanced 2-fold, rather than being inhibited, upon addition of a gp130 blocking antibody.

Conclusion: Our studies indicate that CNTF can activate microglia and dendritic-like microglia similar to IL-6; however, unlike IL-6, CNTF does not stimulate the expected signaling pathways in microglia, nor does it appear to require gp130.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CD40 Antigens / metabolism*
  • Cells, Cultured
  • Ciliary Neurotrophic Factor / metabolism*
  • Ciliary Neurotrophic Factor Receptor alpha Subunit / metabolism*
  • Cyclooxygenase 2 / metabolism
  • Cytokine Receptor gp130 / metabolism
  • Dinoprostone / metabolism*
  • Extracellular Signal-Regulated MAP Kinases / metabolism
  • Genes, MHC Class II / physiology
  • Interferon-gamma / metabolism*
  • Interleukin-6 / metabolism
  • Mice
  • Microglia / metabolism*
  • Phosphorylation
  • Rats
  • STAT3 Transcription Factor / metabolism
  • Tubulin / metabolism
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • CD40 Antigens
  • Ciliary Neurotrophic Factor
  • Ciliary Neurotrophic Factor Receptor alpha Subunit
  • Il6st protein, mouse
  • Interleukin-6
  • STAT3 Transcription Factor
  • Stat3 protein, mouse
  • Tubulin
  • Cytokine Receptor gp130
  • Interferon-gamma
  • Ptgs2 protein, mouse
  • Cyclooxygenase 2
  • Extracellular Signal-Regulated MAP Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Dinoprostone