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Journal of Experimental Medicine Volume 205(8):1889-1901 August 2, 2008. Autoregulation of Th1-mediated inflammation by twist1.
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Journal of Experimental Medicine Volume 205(8):1889-1901 August 2, 2008 Autoregulation of Th1-mediated inflammation by twist1 Uwe Niesner, Inka Albrecht, Marko Janke, Cornelia Doebis, Christoph Loddenkemper, Maria H. Lexberg, Katharina Eulenburg, Stephan Kreher, Juliana Koeck, Ria Baumgrass, Kerstin Bonhagen, Thomas Kamradt, Philipp Enghard, Jens Y. Humrich, Sascha Rutz, Ulf Schulze-Topphoff, Orhan Aktas, Sina Bartfeld, Helena Radbruch, Ahmed N. Hegazy, Max Löhning, Daniel C. Baumgart, Rainer Duchmann, Martin Rudwaleit, Thomas Häupl, Inna Gitelman, Veit Krenn, Joachim Gruen, Jochen Sieper, Martin Zeitz, Bertram Wiedenmann, Frauke Zipp, Alf Hamann, Michal Janitz, Alexander Scheffold, Gerd R. Burmester, Hyun D. Chang, and Andreas Radbruch © 2008 Niesner et.al.
Th cell balance IFNγ Activation STAT4 Production IFNγ Activation Tbet Th1 IL-12 TGFβ IL-1/IL-6/IL-23 IL-17A-F IL-22 Activation RORC2 Th17 naive T cell IL-4 Activation STAT6 Activation GATA3 IL-4 IL-10 IL-13 IL-5 Th2
Twist1: a basic helix-loop-helix transcription factor basic helix-loop-helix transcription factor binds to a consensus sequence called e-box: CANNTG
Repeated Th1 stimulation naive CD4+ CD62L+ T cells from DO11.10 mice (carrying a TCR specific for Ovalbumin) restimulation ... 6d splenic APC Ovalbumin IL-12 anti-IL-4 PMA/iono CD3/CD28 gene array quantitative real-time PCR 38 fold upregulation of twist1 expression in 4 times restimulated Th1 cells
Twist1 expression is induced in Th1, but not Th2 or Th17 cells
Twist1 induction requires IL-12 signaling via STAT4, but not IFN-γ or T-bet
Signaling through NFAT and NF-κB is required for induction of twist1 expression PDTC blocksNF-κB BTP blocks NFAT CSA blocks IL-2 signaling
Generation of Th1 cells constitutively expressing twist1 • d0: splenic DO11.10 cells activated in vitro • d2: infection with twist1 encoding or control retrovirus • d5: sort of GFP+
Genes differentially expressed upon ectopic twist1 overexpression
NF-κB driven luciferase reporter • d0: splenic DO11.10 cells activated in vitro • d2: infection with twist1 or I-κBαM encoding retrovirus • d3: nucleoporation with a mixture of luciferase encoding plasmids • d5: sort of GFP+
Inhibition of NF-κB–mediated signaling by twist1 is promoter-specific
DTH model • 6d-old-Th1 cells overexpressing twist1 injected i.v. in BALB/c • 1d later OVA + IFA injection in footpad • messure of swelling of the footpad
Twist1 knockdown increases inflammatory response in murine arthritis
Conclusions • repeatedly stimulated Th1 cells express twist1 • twist1 expression is NF-κB, NFAT and STAT4 dependent • twist1 is expressed in humans and mice • in Th1 effector memory cells • on CD4+ T cells of inflammed tissue • Tbet is not needed for twist1 expression • twist1 binds to e-boxes in the regulatory regions of specific target genes • twist1 reduces activation-induced expression IL-2, IFN-γ, TNF-α on the protein level and theirby dampening an inflammation