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Dynamic regulatory network controlling TH17 cell differentiation

Nature. 2013 Apr 25;496(7446):461-8. doi: 10.1038/nature11981. Epub 2013 Mar 6.

Abstract

Despite their importance, the molecular circuits that control the differentiation of naive T cells remain largely unknown. Recent studies that reconstructed regulatory networks in mammalian cells have focused on short-term responses and relied on perturbation-based approaches that cannot be readily applied to primary T cells. Here we combine transcriptional profiling at high temporal resolution, novel computational algorithms, and innovative nanowire-based perturbation tools to systematically derive and experimentally validate a model of the dynamic regulatory network that controls the differentiation of mouse TH17 cells, a proinflammatory T-cell subset that has been implicated in the pathogenesis of multiple autoimmune diseases. The TH17 transcriptional network consists of two self-reinforcing, but mutually antagonistic, modules, with 12 novel regulators, the coupled action of which may be essential for maintaining the balance between TH17 and other CD4(+) T-cell subsets. Our study identifies and validates 39 regulatory factors, embeds them within a comprehensive temporal network and reveals its organizational principles; it also highlights novel drug targets for controlling TH17 cell differentiation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Differentiation / genetics*
  • Cells, Cultured
  • DNA / genetics
  • DNA / metabolism
  • Forkhead Transcription Factors / metabolism
  • Gene Knockdown Techniques
  • Gene Regulatory Networks / genetics*
  • Genome / genetics
  • Interferon-gamma / biosynthesis
  • Interleukin-2 / genetics
  • Mice
  • Mice, Inbred C57BL
  • Nanowires
  • Neoplasm Proteins / metabolism
  • Nuclear Proteins / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Reproducibility of Results
  • Silicon
  • Th17 Cells / cytology*
  • Th17 Cells / immunology
  • Th17 Cells / metabolism*
  • Time Factors
  • Trans-Activators / metabolism
  • Transcription Factors / metabolism
  • Transcription, Genetic / genetics
  • fas Receptor / metabolism

Substances

  • Dsip1 protein, mouse
  • Forkhead Transcription Factors
  • Foxp3 protein, mouse
  • Interleukin-2
  • Mina53 protein, mouse
  • Neoplasm Proteins
  • Nuclear Proteins
  • Pou2af1 protein, mouse
  • RNA, Messenger
  • Trans-Activators
  • Transcription Factors
  • fas Receptor
  • Interferon-gamma
  • DNA
  • Silicon

Associated data

  • GEO/GSE43948
  • GEO/GSE43949
  • GEO/GSE43955
  • GEO/GSE43969