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Resveratrol differentially modulates inflammatory responses of microglia and astrocytes

  1. Author:
    Lu, X. F.
    Ma, L. L.
    Ruan, L. F.
    Kong, Y.
    Mou, H. W.
    Zhang, Z. J.
    Wang, Z. J.
    Wang, J. M.
    Le, Y. Y.
  2. Author Address

    [Lu, Xiaofeng; Ma, Lili; Ruan, Lingfei; Kong, Yan; Mou, Haiwei; Zhang, Zhijie; Le, Yingying] Chinese Acad Sci, Key Lab Nutr & Metab, Inst Nutr Sci, Shanghai Inst Biol Sci, Shanghai 200031, Peoples R China. [Ruan, Lingfei; Kong, Yan; Mou, Haiwei; Le, Yingying] Chinese Acad Sci, Grad Sch, Shanghai 200031, Peoples R China. [Wang, Ji Ming] NCI, Mol Immunoregulat Lab, Canc & Inflammat Program, Ctr Canc Res, Frederick, MD 21701 USA. [Wang, Zhijun] Chinese Acad Sci, Shanghai Synchrotron Radiat Facil, Shanghai Inst Appl Phys, Shanghai 201204, Peoples R China.;Le, YY, Chinese Acad Sci, Key Lab Nutr & Metab, Inst Nutr Sci, Shanghai Inst Biol Sci, Shanghai 200031, Peoples R China.;yyle@sibs.ac.cn
    1. Year: 2010
    2. Date: Aug
  1. Journal: Journal of Neuroinflammation
    1. 7
    2. Pages: 14
  2. Type of Article: Article
  3. Article Number: 46
  4. ISSN: 1742-2094
  1. Abstract:

    Background: Inflammatory responses in the CNS mediated by activated glial cells play an important role in host-defense but are also involved in the development of neurodegenerative diseases. Resveratrol is a natural polyphenolic compound that has cardioprotective, anticancer and anti-inflammatory properties. We investigated the capacity of resveratrol to protect microglia and astrocyte from inflammatory insults and explored mechanisms underlying different inhibitory effects of resveratrol on microglia and astrocytes. Methods: A murine microglia cell line (N9), primary microglia, or astrocytes were stimulated by LPS with or without different concentrations of resveratrol. The expression and release of proinflammatory cytokines (TNF-alpha, IL-1 beta, IL-6, MCP-1) and iNOS/NO by the cells were measured by PCR/real-time PCR and ELISA, respectively. The phosphorylation of the MAP kinase superfamily was analyzed by western blotting, and activation of NF-kappa B and AP-1 was measured by luciferase reporter assay and/or electrophoretic mobility shift assay. Results: We found that LPS stimulated the expression of TNF-alpha, IL-1 beta, IL-6, MCP-1 and iNOS in murine microglia and astrocytes in which MAP kinases, NF-kappa B and AP-1 were differentially involved. Resveratrol inhibited LPS-induced expression and release of TNF-alpha, IL-6, MCP-1, and iNOS/NO in both cell types with more potency in microglia, and inhibited LPS-induced expression of IL-1 beta in microglia but not astrocytes. Resveratrol had no effect on LPS-stimulated phosphorylation of ERK1/2 and p38 in microglia and astrocytes, but slightly inhibited LPS-stimulated phosphorylation of JNK in astrocytes. Resveratrol inhibited LPS-induced NF-kappa B activation in both cell types, but inhibited AP-1 activation only in microglia. Conclusion: These results suggest that murine microglia and astrocytes produce proinflammatory cytokines and NO in response to LPS in a similar pattern with some differences in signaling molecules involved, and further suggest that resveratrol exerts anti-inflammatory effects in microglia and astrocytes by inhibiting different proinflammatory cytokines and key signaling molecules.

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External Sources

  1. DOI: 10.1186/1742-2094-7-46
  2. WOS: 000282385200001

Library Notes

  1. Fiscal Year: FY2009-2010
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