Abstract
Th17 cells promote inflammatory reactions, whereas regulatory T (Treg) cells inhibit them. Thus, the Th17/Treg cell balance is critically important in inflammatory diseases. However, the molecular mechanisms underlying this balance are unclear. Here, we demonstrate that casein kinase 2 (CK2) is a critical determinant of the Th17/Treg cell balance. Both the inhibition of CK2 with a specific pharmacological inhibitor, CX-4945, and its small hairpin RNA (shRNA)-mediated knockdown suppressed Th17 cell differentiation but reciprocally induced Treg cell differentiation in vitro. Moreover, CX-4945 ameliorated the symptoms of experimental autoimmune encephalomyelitis and reduced Th17 cell infiltration into the central nervous system. Mechanistically, CX-4945 inhibited the IL-6/STAT3 and Akt/mTOR signaling pathways. Thus, CK2 has a crucial role in regulating the Th17/Treg balance.
MeSH terms
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Animals
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Casein Kinase II / antagonists & inhibitors
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Casein Kinase II / genetics
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Casein Kinase II / metabolism*
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Cell Differentiation* / genetics
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Cell Differentiation* / immunology
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Encephalomyelitis, Autoimmune, Experimental
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Female
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Gene Expression
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Gene Knockdown Techniques
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Lymphocyte Activation / genetics
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Lymphocyte Activation / immunology
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Lymphocyte Count
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Mice
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Phosphorylation
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Proto-Oncogene Proteins c-akt / metabolism
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RNA Interference
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Receptors, Interleukin-6 / metabolism
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STAT3 Transcription Factor / metabolism
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Signal Transduction
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T-Lymphocyte Subsets / cytology
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T-Lymphocyte Subsets / immunology
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T-Lymphocyte Subsets / metabolism
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T-Lymphocytes, Regulatory / cytology*
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T-Lymphocytes, Regulatory / immunology
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T-Lymphocytes, Regulatory / metabolism*
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TOR Serine-Threonine Kinases
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Th17 Cells / cytology*
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Th17 Cells / immunology
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Th17 Cells / metabolism*
Substances
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Receptors, Interleukin-6
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STAT3 Transcription Factor
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Casein Kinase II
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Proto-Oncogene Proteins c-akt
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TOR Serine-Threonine Kinases