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General nature of the STAT3-activated anti-inflammatory response
Authors:El Kasmi Karim C  Holst Jeff  Coffre Maryaline  Mielke Lisa  de Pauw Antoine  Lhocine Nouara  Smith Amber M  Rutschman Robert  Kaushal Deepak  Shen Yuhong  Suda Takashi  Donnelly Raymond P  Myers Martin G  Alexander Warren  Vignali Dario A A  Watowich Stephanie S  Ernst Matthias  Hilton Douglas J  Murray Peter J
Institution:Department of Infectious Diseases, St. Jude's Children's Research Hospital, Memphis, TN 38105, USA.
Abstract:Although many cytokine receptors generate their signals via the STAT3 pathway, the IL-10R appears unique in promoting a potent anti-inflammatory response (AIR) via STAT3 to antagonize proinflammatory signals that activate the innate immune response. We found that heterologous cytokine receptor systems that activate STAT3 but are naturally refractory (the IL-22R), or engineered to be refractory (the IL-6, leptin, and erythropoietin receptors), to suppressor of cytokine signaling-3-mediated inhibition activate an AIR indistinguishable from IL-10. We conclude that the AIR is a generic cytokine signaling pathway dependent on STAT3 but not unique to the IL-10R.
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