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Rbpj expression in regulatory T cells is critical for restraining TH2 responses.

Michael DelacherChristian SchmidlYonatan HerzigMinka BreloerWiebke HartmannFabian BrunkDanny KägebeinUlrike TrägerAnn-Cathrin HoferSebastian BittnerDieter WeichenhanCharles D ImbuschAgnes Hotz-WagenblattThomas HielscherAchim BreilingGiuseppina FedericoHermann-Josef GröneRoland M SchmidMichael RehliJakub AbramsonMarkus Feuerer
Published in: Nature communications (2019)
The transcriptional regulator Rbpj is involved in T-helper (TH) subset polarization, but its function in Treg cells remains unclear. Here we show that Treg-specific Rbpj deletion leads to splenomegaly and lymphadenopathy despite increased numbers of Treg cells with a polyclonal TCR repertoire. A specific defect of Rbpj-deficient Treg cells in controlling TH2 polarization and B cell responses is observed, leading to the spontaneous formation of germinal centers and a TH2-associated immunoglobulin class switch. The observed phenotype is environment-dependent and can be induced by infection with parasitic nematodes. Rbpj-deficient Treg cells adopt open chromatin landscapes and gene expression profiles reminiscent of tissue-derived TH2-polarized Treg cells, with a prevailing signature of the transcription factor Gata-3. Taken together, our study suggests that Treg cells require Rbpj to specifically restrain TH2 responses, including their own excessive TH2-like differentiation potential.
Keyphrases
  • induced apoptosis
  • transcription factor
  • cell cycle arrest
  • regulatory t cells
  • gene expression
  • signaling pathway
  • minimally invasive
  • dna methylation
  • body mass index
  • long non coding rna
  • dna damage
  • weight loss