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Blimp1 Prevents Methylation of Foxp3 and Loss of Regulatory T Cell Identity at Sites of Inflammation

  • Garima Garg
  • , Andreas Muschaweckh
  • , Helena Moreno
  • , Ajithkumar Vasanthakumar
  • , Stefan Floess
  • , Gildas Lepennetier
  • , Rupert Oellinger
  • , Yifan Zhan
  • , Tommy Regen
  • , Michael Hiltensperger
  • , Christian Peter
  • , Lilian Aly
  • , Benjamin Knier
  • , Lakshmi Reddy Palam
  • , Reuben Kapur
  • , Mark H. Kaplan
  • , Ari Waisman
  • , Roland Rad
  • , Gunnar Schotta
  • , Jochen Huehn
  • Axel Kallies, Thomas Korn
  • Technical University of Munich
  • University of Munich
  • University of Melbourne
  • and University of Melbourne Department of Medical Biology and School of Mathematics and Statistics
  • Helmholtz Centre for Infection Research (HZI)
  • University Medical Center
  • Munich Cluster for Systems Neurology (SyNergy)
  • Indiana University School of Medicine

Research output: Contribution to journalArticlepeer-review

108 Scopus citations

Abstract

An inflammatory environment threatens the stability of Foxp3 + Treg cells. Garg et al. show that by expressing the transcriptional regulator Blimp1, Treg cells resist the IL-6-driven loss of Foxp3 in inflamed tissues. Blimp1 prevents the methylation and reduced expression of Foxp3 through inhibition of the methyltransferase Dnmt3a.

Original languageEnglish
Pages (from-to)1854-1868.e5
JournalCell Reports
Volume26
Issue number7
DOIs
StatePublished - 12 Feb 2019

Keywords

  • Blimp1
  • CNS
  • CNS2
  • DNA methyltransferases
  • Foxp3
  • Interleukin-6
  • epigenetic regulation
  • inflammation
  • regulatory T cells

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