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PubMed_Structured_Abstracts

Id Subject Object Predicate Lexical cue
T1 197-422 OBJECTIVE denotes To examine the role of interleukin-23 (IL-23) in subgroup polarization of IL-17A-positive and/or interferon-gamma (IFNgamma)-positive T cells in autoimmune disease-prone DBA/1 mice with and without collagen-induced arthritis.
T2 432-927 METHODS denotes A magnetic-activated cell sorting system was used to isolate CD4+ T cells from the spleen of naive and type II collagen (CII)-immunized DBA/1 mice. These CD4+ T cells were stimulated in vitro under Th0, Th1, or different Th17 culture conditions. Intracellular staining for IL-17A and IFNgamma was evaluated by flow cytometry. In addition, Th17 cytokines and T helper-specific transcription factors were analyzed by enzyme-linked immunosorbent assay and/or quantitative polymerase chain reaction.
T3 937-1885 RESULTS denotes In CD4+ T cells from naive DBA/1 mice, IL-23 alone hardly induced retinoic acid-related orphan receptor gammat (RORgammat), Th17 polarization, and Th17 cytokines, but it inhibited T-bet expression. In contrast, transforming growth factor beta1 (TGFbeta1)/IL-6 was a potent inducer of RORgammat, RORalpha, IL-17A, IL-17F, IL-21, and FoxP3 in these cells. In contrast to TGFbeta1/IL-6, IL-23 was critical for the induction of IL-22 in CD4+ T cells from both naive and CII-immunized DBA/1 mice. Consistent with these findings, IL-23 showed a more pronounced induction of the IL-17A+IFNgamma- subset in CD4+ T cells from CII-immunized mice. However, in CD4+ T cells from naive mice, IL-23 significantly increased the TGFbeta1/IL-6-induced Th17 polarization, including elevated levels of IL-17A and IL-17F and decreased expression of T-bet and FoxP3. Of note, the IL-23-induced increase in IL-17A and IL-17F levels was prevented in T-bet-deficient mice.
T4 1898-2219 CONCLUSIONS denotes IL-23 promotes Th17 differentiation by inhibiting T-bet and FoxP3 and is required for elevation of IL-22, but not IL-21, levels in autoimmune arthritis. These data indicate different mechanisms for IL-23 and TGFbeta1/IL-6 at the transcription factor level during Th17 differentiation in autoimmune experimental arthritis.

PubmedHPO

Id Subject Object Predicate Lexical cue
T1 342-360 HP_0002960 denotes autoimmune disease
T2 342-352 HP_0002960 denotes autoimmune
T3 412-421 HP_0001369 denotes arthritis

Allie

Id Subject Object Predicate Lexical cue
SS1_20131264_2_0 220-234 expanded denotes interleukin-23
SS2_20131264_2_0 236-241 abbr denotes IL-23
SS1_20131264_2_1 294-310 expanded denotes interferon-gamma
SS2_20131264_2_1 312-320 abbr denotes IFNgamma
SS1_20131264_4_0 500-551 expanded denotes cells from the spleen of naive and type II collagen
SS2_20131264_4_0 553-556 abbr denotes CII
SS1_20131264_9_0 1012-1047 expanded denotes acid-related orphan receptor gammat
SS2_20131264_9_0 1049-1058 abbr denotes RORgammat
SS1_20131264_10_0 1148-1180 expanded denotes transforming growth factor beta1
SS2_20131264_10_0 1182-1190 abbr denotes TGFbeta1
AE1_20131264_2_0 SS1_20131264_2_0 SS2_20131264_2_0 abbreviatedTo interleukin-23,IL-23
AE1_20131264_2_1 SS1_20131264_2_1 SS2_20131264_2_1 abbreviatedTo interferon-gamma,IFNgamma
AE1_20131264_4_0 SS1_20131264_4_0 SS2_20131264_4_0 abbreviatedTo cells from the spleen of naive and type II collagen,CII
AE1_20131264_9_0 SS1_20131264_9_0 SS2_20131264_9_0 abbreviatedTo acid-related orphan receptor gammat,RORgammat
AE1_20131264_10_0 SS1_20131264_10_0 SS2_20131264_10_0 abbreviatedTo transforming growth factor beta1,TGFbeta1

2015-BEL-Sample-2

Id Subject Object Predicate Lexical cue
BEL:20034538 1574-1884 complex(p(MGI:Il12b),p(MGI:Il23a)) decreases r(MGI:Foxp3) denotes However, in CD4+ T cells from naive mice, IL-23 significantly increased the TGFbeta1/IL-6-induced Th17 polarization, including elevated levels of IL-17A and IL-17F and decreased expression of T-bet and FoxP3. Of note, the IL-23-induced increase in IL-17A and IL-17F levels was prevented in T-bet-deficient mice
BEL:20034542 1574-1884 complex(p(MGI:Il12b),p(MGI:Il23a)) increases r(MGI:Il17a) denotes However, in CD4+ T cells from naive mice, IL-23 significantly increased the TGFbeta1/IL-6-induced Th17 polarization, including elevated levels of IL-17A and IL-17F and decreased expression of T-bet and FoxP3. Of note, the IL-23-induced increase in IL-17A and IL-17F levels was prevented in T-bet-deficient mice
BEL:20034546 1574-1884 complex(p(MGI:Il12b),p(MGI:Il23a)) increases r(MGI:Il17f) denotes However, in CD4+ T cells from naive mice, IL-23 significantly increased the TGFbeta1/IL-6-induced Th17 polarization, including elevated levels of IL-17A and IL-17F and decreased expression of T-bet and FoxP3. Of note, the IL-23-induced increase in IL-17A and IL-17F levels was prevented in T-bet-deficient mice
BEL:20034550 1291-1427 complex(p(MGI:Il12b),p(MGI:Il23a)) increases r(MGI:Il22) denotes In contrast to TGFbeta1/IL-6, IL-23 was critical for the induction of IL-22 in CD4+ T cells from both naive and CII-immunized DBA/1 mice
BEL:20034564 935-1133 complex(p(MGI:Il23a),p(MGI:Il1b)) decreases r(MGI:Tbx21) denotes : In CD4+ T cells from naive DBA/1 mice, IL-23 alone hardly induced retinoic acid-related orphan receptor gammat (RORgammat), Th17 polarization, and Th17 cytokines, but it inhibited T-bet expression