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Human Macrophage Migration Inhibitory Factor
- Source :
- Journal of Biological Chemistry. 281:29641-29651
- Publication Year :
- 2006
- Publisher :
- Elsevier BV, 2006.
-
Abstract
- Macrophage migration inhibitory factor (MIF) is a pro-inflammatory mediator with the ability to induce various immunomodulatory responses and override glucocorticoid-driven immunosuppression. Some of these functions have been linked to the unusual enzymatic properties of the protein, namely tautomerase and oxidoreductase activities. However, there are conflicting reports regarding the functional role of these enzymatic properties in normal physiological homeostasis and disease progression. Therefore, we have produced a highly pure, virtually endotoxin-free recombinant MIF preparation and fully characterized this using a variety of biochemical and biophysical approaches. The recombinant protein, with demonstrable enzymatic activity, was then used to systematically examine the biological activity of MIF. Surprisingly, treatment with MIF alone failed to induce cytokine expression, with the exception of IL-8. However, co-treatment of lipopolysaccharide (LPS) in conjunction with MIF produced synergistic secretion of tumor necrosis factor-alpha, interleukin (IL)-1, and IL-8 compared with LPS alone. The potentiating effect of MIF was seen at physiologically relevant concentrations. These data suggest that MIF has no conventional cytokine activity but, rather, acts to modulate and amplify the response to LPS.
- Subjects :
- Lipopolysaccharide
medicine.medical_treatment
Interleukin
Biological activity
Cell Biology
Biology
Biochemistry
Cell biology
chemistry.chemical_compound
Cytokine
Mediator
chemistry
otorhinolaryngologic diseases
medicine
Secretion
Macrophage migration inhibitory factor
Tumor necrosis factor alpha
Molecular Biology
Subjects
Details
- ISSN :
- 00219258
- Volume :
- 281
- Database :
- OpenAIRE
- Journal :
- Journal of Biological Chemistry
- Accession number :
- edsair.doi...........6883407bfddeebf79f298659418c6376
- Full Text :
- https://doi.org/10.1074/jbc.m601103200