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PMID |
Sentence |
| 1 |
15145618
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Treatment with interferon-gamma (IFN-g) induced SOCS-1 and enhanced SOCS-3 expression, and was associated with decreased tumor necrosis factor-alpha (TNF) and increased leukemia inhibitory factor (LIF) in culture supernatants.
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| 2 |
15145618
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Treatment with conditioned medium from myelin basic protein-stimulated encephalitogenic lymphoid cells (MBP-CM) increased SOCS-3 and induced SOCS-1 expression.
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| 3 |
16373362
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Suppressor of cytokine signaling (SOCS)-1 and SOCS-3 are members of a family of inducible intracellular proteins that negatively regulate cytokine signaling in cells of hematopoietic origin and may influence the Th1 to Th2 balance.
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| 4 |
16373362
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SOCS-1 and SOCS-3 are induced by cytokines that are known to be up-regulated during EAE, including IFN-gamma (IFN-g) and IL-6, respectively.
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| 5 |
16373362
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To test the hypothesis that the level of induction of SOCS-1 and SOCS-3 correlates with the course of EAE, mRNA levels were compared in spinal cords of SJL and B6 mice during discrete stages of disease.
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| 6 |
16373362
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SOCS-1 and SOCS-3 were elevated throughout active disease in both strains.
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| 7 |
16373362
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At peak EAE, SOCS-1 was higher and SOCS-3 was lower in B6 cords compared with SJL cords.
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| 8 |
16373362
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This correlated with greater expression of the Th1 cytokine, IFN-g, and less of the Th2 cytokine, IL-10, in B6 cords relative to SJL cords during onset and peak disease.
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| 9 |
16373362
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SOCS-3 inducers in the IL-6 family were expressed differentially between the strains.
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| 10 |
16373362
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IL-6 and leukemia inhibitory factor were higher at onset in B6 cords whereas ciliary neurotrophic factor was increased in SJL cords during peak disease.
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| 11 |
21518797
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The lineage-defining factors T-bet and Bcl-6 collaborate to regulate Th1 gene expression patterns.
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| 12 |
21518797
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The T-box transcription factor T-bet is important for the differentiation of naive CD4(+) T helper cells (Th cells) into the Th1 phenotype.
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| 13 |
21518797
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In this study, we first identify Socs1, Socs3, and Tcf7 (TCF-1) as gene targets that are negatively regulated by T-bet.
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| 14 |
21518797
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Consistent with this, we identified two T-bet DNA-binding elements in the Socs1 promoter that are functionally used to down-regulate transcription in primary Th1 cells.
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| 15 |
21518797
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Furthermore, T-bet functionally recruits Bcl-6 to the Ifng locus in late stages of Th1 differentiation to repress its activity, possibly to prevent the overproduction of IFN-γ, which could result in autoimmunity.
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