+1 Recommend
0 collections
      • Record: found
      • Abstract: found
      • Article: not found

      Macrophage migration inhibitory factor (MIF) sustains macrophage proinflammatory function by inhibiting p53: regulatory role in the innate immune response.

      Proceedings of the National Academy of Sciences of the United States of America

      Animals, Apoptosis, Arachidonic Acid, metabolism, Blotting, Western, Cell Survival, Cyclooxygenase 2, Dinoprostone, Endotoxins, pharmacology, Enzyme-Linked Immunosorbent Assay, Genes, Dominant, Isoenzymes, biosynthesis, Luciferases, Macrophage Migration-Inhibitory Factors, genetics, Macrophages, immunology, Male, Mice, Mice, Transgenic, Plasmids, Prostaglandin-Endoperoxide Synthases, Recombinant Fusion Proteins, Transfection, Tumor Necrosis Factor-alpha, Tumor Suppressor Protein p53, antagonists & inhibitors

      Read this article at

          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.


          The importance of the macrophage in innate immunity is underscored by its secretion of an array of powerful immunoregulatory and effector molecules. We report herein that macrophage migration inhibitory factor (MIF), a product of activated macrophages, sustains macrophage survival and function by suppressing activation-induced, p53-dependent apoptosis. Endotoxin administration to MIF(-/-) mice results in decreased macrophage viability, decreased proinflammatory function, and increased apoptosis when compared with wild-type controls. Moreover, inhibition of p53 in endotoxin-treated, MIF-deficient macrophages suppresses enhanced apoptosis and restores proinflammatory function. MIF inhibits p53 activity in macrophages via an autocrine regulatory pathway, resulting in a decrease in cellular p53 accumulation and subsequent function. Inhibition of p53 by MIF coincides with the induction of arachidonic acid metabolism and cyclooxygenase-2 (Cox-2) expression, which is required for MIF regulation of p53. MIF's effect on macrophage viability and survival provides a previously unrecognized mechanism to explain its critical proinflammatory action in conditions such as sepsis, and suggests new approaches for the modulation of innate immune responses.

          Related collections

          Author and article information



          Comment on this article