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Details

Autor(en) / Beteiligte
Titel
Curcumin Suppresses Janus Kinase-STAT Inflammatory Signaling through Activation of Src Homology 2 Domain-Containing Tyrosine Phosphatase 2 in Brain Microglia
Ist Teil von
  • The Journal of immunology (1950), 2003-12, Vol.171 (11), p.6072-6079
Ort / Verlag
United States: Am Assoc Immnol
Erscheinungsjahr
2003
Quelle
MEDLINE
Beschreibungen/Notizen
  • Curcumin has been strongly implicated as an anti-inflammatory agent, but the precise mechanisms of its action are largely unknown. In this study, we show that the inhibitory action of curcumin on Janus kinase (JAK)-STAT signaling can contribute to its anti-inflammatory activity in the brain. In both rat primary microglia and murine BV2 microglial cells, curcumin effectively suppressed the ganglioside-, LPS-, or IFN-gamma-stimulated induction of cyclooxygenase-2 and inducible NO synthase, important enzymes that mediate inflammatory processes. These anti-inflammatory effects appear to be due, at least in part, to the suppression of the JAK-STAT inflammatory signaling cascade. Curcumin markedly inhibited the phosphorylation of STAT1 and 3 as well as JAK1 and 2 in microglia activated with gangliosides, LPS, or IFN-gamma. Curcumin consistently suppressed not only NF binding to IFN-gamma-activated sequence/IFN-stimulated regulatory element, but also the expression of inflammation-associated genes, including ICAM-1 and monocyte chemoattractant protein 1, whose promoters contain STAT-binding elements. We further show that activation of Src homology 2 domain-containing protein tyrosine phosphatases (SHP)-2, a negative regulator of JAK activity, is likely to be one of the mechanisms underlying the curcumin-mediated inhibition of JAK-STAT signaling. Treatment of microglial cells with curcumin led to an increase in phosphorylation and association with JAK1/2 of SHP-2, which inhibit the initiation of JAK-STAT inflammatory signaling in activated microglia. Taken together, these data suggest curcumin suppresses JAK-STAT signaling via activation of SHP-2, thus attenuating inflammatory response of brain microglial cells.
Sprache
Englisch
Identifikatoren
ISSN: 0022-1767
eISSN: 1550-6606
DOI: 10.4049/jimmunol.171.11.6072
Titel-ID: cdi_proquest_miscellaneous_71378497
Format
Schlagworte
Animals, Anti-Inflammatory Agents, Non-Steroidal - pharmacology, Brain - drug effects, Brain - enzymology, Brain - metabolism, Brain - pathology, Cells, Cultured, Curcumin - pharmacology, Cyclooxygenase 2, DNA-Binding Proteins - antagonists & inhibitors, DNA-Binding Proteins - metabolism, DNA-Binding Proteins - physiology, Down-Regulation - drug effects, Gene Expression Regulation - drug effects, Inflammation - genetics, Inflammation - metabolism, Inflammation - prevention & control, Interferon-gamma - antagonists & inhibitors, Interferon-gamma - metabolism, Interferon-gamma - pharmacology, Intracellular Signaling Peptides and Proteins, Isoenzymes - antagonists & inhibitors, Isoenzymes - biosynthesis, Janus Kinase 1, Janus Kinase 2, Microglia - drug effects, Microglia - enzymology, Microglia - metabolism, Microglia - pathology, Nitric Oxide Synthase - antagonists & inhibitors, Nitric Oxide Synthase - biosynthesis, Nitric Oxide Synthase Type II, Phosphorylation - drug effects, Prostaglandin-Endoperoxide Synthases - biosynthesis, Protein Phosphatase 2, Protein Tyrosine Phosphatase, Non-Receptor Type 11, Protein Tyrosine Phosphatases - metabolism, Protein-Tyrosine Kinases - antagonists & inhibitors, Protein-Tyrosine Kinases - metabolism, Protein-Tyrosine Kinases - physiology, Proto-Oncogene Proteins, Rats, Rats, Sprague-Dawley, Regulatory Sequences, Nucleic Acid, SH2 Domain-Containing Protein Tyrosine Phosphatases, Signal Transduction - drug effects, Signal Transduction - physiology, src Homology Domains - physiology, STAT1 Transcription Factor, STAT3 Transcription Factor, Trans-Activators - antagonists & inhibitors, Trans-Activators - metabolism, Trans-Activators - physiology, Up-Regulation - drug effects

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