(B) Western blot analysis of nuclear fractions of primary CD4+ lymphocytes from FoxP3-IRES-GFP reporter mice. Cells were treated 1 hour with 4 μg/ml of anti-CD3 and 1 μg/ml of anti-CD28 this website antibodies. (A, B) Lamin B used as loading control. Data shown are representative of two experiments. C, D. Analysis of nuclear transcription factors and chromatin conformation at theTNF TSS in primary CD4+ T cells. Effect of Cyclosporine A (CsA), JNK inhibitor SP600125 (C) and protein synthesis inhibitor Anisomycin (D) on nuclear concentrations of NFATc2 and c-Jun (top) and chromatin conformation at TNF TSS (middle and bottom). (C) Cells were pretreated 1 hour with indicated concentrations

of CsA and SP600125 and treated 1 hour with 4 μg/ml of anti-CD3 and 1 μg/ml of anti-CD28 antibodies. (D) Cells were treated 1 hour with indicated concentrations of Anisomycin or with 4 μg/ml of anti-CD3 and 1 μg/ml of anti-CD28 antibodies. (C, D) Western blot analysis. Lamin B used as loading control and data shown are representative of two experiments. Extra lanes were deleted from the blot image (C) between lanes 2 and 3,

3 and 4 (top). Relative resistance to MNase digestion at the TNF TSS (amplicon -50+73) calculated and normalized to control MNase-digested genomic DNA and average of signals for amplicons +67+189 and +121+240. Data are shown as mean ± SD of five (C) or two (D) experiments. Statistical significance determined by Student’s T-test. E, F. Analysis of nuclear transcription factors and chromatin conformation at theTNF TSS in primary CD4+ T cells Effect of Cyclosporine A (CsA), JNK inhibitor SP600125 (E) and Selleckchem Ribociclib protein synthesis inhibitor Anisomycin chromatin conformation at TNF TSS (F) (profile of MNase resistance around TNF TSS (-124 +240) normalized only to control MNase-digested genomic DNA). (E) Cells were pretreated 1 hour with indicated concentrations of CsA and SP600125 and treated 1 hour with 4 μg/ml of anti-CD3 and 1 μg/ml of anti-CD28 antibodies. (F) Cells were treated 1 hour with indicated concentrations of Anisomycin or with 4 μg/ml of anti-CD3

and 1 μg/ml of anti-CD28 Montelukast Sodium antibodies. (E, F) Relative resistance to MNase digestion at the TNF TSS (amplicon -50+73) calculated and primary data representative of five (E) or two (F) experiments are shown. Figure S6. Effect of CsA and SP600125 on chromatin conformation around TNF TSS (-124 +240) in quiescent polarized T cells Th2s and Th17s cells were polarized in the presence of soluble anti-CD3 antibodies, Th1i – in presence of immobilized anti-CD3 antibodies. After polarization cells were cultured in the medium without cytokines or antibodies for 12 hours with indicated concentrations of inhibitors. Examples of primary data normalized only to control MNase-digested genomic DNA are representative of two (Th2s) and three (Th1i and Th17s) experiments. Centers of amplicons covering TNF TSS are labeled with arrows. Figure S7.