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      Possible new role for NF-kappaB in the resolution of inflammation.

      Nature medicine
      Animals, Anti-Infective Agents, pharmacology, Anti-Inflammatory Agents, Non-Steroidal, metabolism, Apoptosis, Carrageenan, adverse effects, Cysteine Endopeptidases, Female, Granuloma, chemically induced, immunology, Inflammation, Leukocytes, Leupeptins, Male, Mice, Multienzyme Complexes, antagonists & inhibitors, NF-kappa B, Nitriles, Pleurisy, Proteasome Endopeptidase Complex, Protein Binding, drug effects, Proto-Oncogene Proteins, biosynthesis, Proto-Oncogene Proteins c-bcl-2, Pyrrolidines, Rats, Sulfones, Thiocarbamates, Transforming Growth Factor beta, secretion, Transforming Growth Factor beta1, Tumor Suppressor Protein p53, bcl-2-Associated X Protein

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          Abstract

          Inflammation involves the sequential activation of signaling pathways leading to the production of both pro- and anti-inflammatory mediators. Although much attention has focused on pro-inflammatory pathways that initiate inflammation, relatively little is known about the mechanisms that switch off inflammation and resolve the inflammatory response. The transcription factor NF-kappaB is thought to have a central role in the induction of pro-inflammatory gene expression and has attracted interest as a new target for the treatment of inflammatory disease. We show here that NF-kappaB activation in leukocytes recruited during the onset of inflammation is associated with pro-inflammatory gene expression, whereas such activation during the resolution of inflammation is associated with the expression of anti-inflammatory genes and the induction of apoptosis. Inhibition of NF-kappaB during the resolution of inflammation protracts the inflammatory response and prevents apoptosis. This suggests that NF-kappaB has an anti-inflammatory role in vivo involving the regulation of inflammatory resolution.

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