Abstract
Gliomas are highly aggressive and accompanied by numerous microglia/macrophages (MG/MP) in and about the tumor. Little is known about what MG/MP do in this setting, or whether modulating MG/MP activation might affect glioma progression. Here, we used a glioma-microglia in culture system to establish the effects the tumor and microglia have on each other. We assessed glioma progression in vivo after MG/MP ablation or in the setting of exaggerated MG/MP activation. We show that glioma cells activate microglia but inhibit their phagocytic activities. Local ablation of MG/MP in vivo decreased tumor size and improved survival curves. Conversely, pharmacological activation of MG/MP increased glioma size through stimulating tumor proliferation and inhibiting apoptosis. In agreement with recent reports, expression of the chemokine CCL21 is enhanced after MG/MP activation and correlates with tumor growth. Taken together, our findings demonstrate that inhibition of MG/MP activation may constitute a new and effective contribution towards suppressing glioma proliferation.
| Original language | English |
|---|---|
| Pages (from-to) | 472-485 |
| Number of pages | 14 |
| Journal | GLIA |
| Volume | 59 |
| Issue number | 3 |
| DOIs | |
| State | Published - Mar 2011 |
Keywords
- Ablation
- Glioma
- Mice
- Microglia
- MIF/TKP-tuftsin fragment 1-3
- Tuftsin
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