Macrophage inhibitory factor: Difference between revisions

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<StructureSection load='2ooh' size='350' side='right' caption='Structure of human macrophage inhibitory factor trimer complex with inhibitor, glycerol and sulfate (PDB entry [[2ooh]])' scene=''>
<StructureSection load='2ooh' size='350' side='right' caption='Structure of human macrophage inhibitory factor trimer complex with inhibitor, glycerol and sulfate (PDB entry [[2ooh]])' scene=''>
== Function ==
== Function ==
'''Macrophage inhibitory factor''' (MIF) is an inflammatory cytokine.  MIF is released to the blood stream upon stimulation of white blood cells by bacterial antigens<ref>PMID:11032394</ref>.  MIF contains two different catalytic sites.  A phenylpyruvate tautomerase site is located in the N terminal.  A disulfide reductase site is located in the tetrapeptide Cys-Ala-Leu-Cys in position 57-60.
'''Macrophage inhibitory factor''' (MIF) is an inflammatory cytokine.  MIF is released to the blood stream upon stimulation of white blood cells by bacterial antigens<ref>PMID:11032394</ref>.   


== Relevance ==
== Relevance ==
MIF plays a role in various solid and hematologic tumors<ref>PMID:19326434</ref>.  MIF is overexpressed in various tumors and is suggested to be the molecular link between chronic inflammation and cancer.  MIF has a role in skin inflammation, immune response, disease, tumorigenesis and wound healing<ref>PMID:15659324</ref>.  MIF has a role in Alzheimer disease and its inhibition may prevent the disease onset<ref>PMID:20200619</ref>.  
MIF plays a role in various solid and hematologic tumors<ref>PMID:19326434</ref>.  MIF is overexpressed in various tumors and is suggested to be the molecular link between chronic inflammation and cancer.  MIF has a role in skin inflammation, immune response, disease, tumorigenesis and wound healing<ref>PMID:15659324</ref>.  MIF has a role in Alzheimer disease and its inhibition may prevent the disease onset<ref>PMID:20200619</ref>.  
== Structural highlights ==
MIF contains two different catalytic sites.  A phenylpyruvate tautomerase site is located in the N terminal.  A disulfide reductase site is located in the tetrapeptide Cys-Ala-Leu-Cys in position 57-60.  The inhibitor binds to the pro-inflammatory tautomerase site<ref>PMID:17526494</ref>.
</StructureSection>
</StructureSection>


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Michal Harel, Alexander Berchansky