Transcriptional and epigenetic networks of helper T and innate lymphoid cells

Han Yu Shih, Giuseppe Sciumè, Amanda C. Poholek, Golnaz Vahedi, Kiyoshi Hirahara, Alejandro V. Villarino, Michael Bonelli, Remy Bosselut, Yuka Kanno, Stefan A. Muljo, John J. O'Shea

Research output: Contribution to journalArticlepeer-review

60 Scopus citations

Abstract

Summary: The discovery of the specification of CD4+ helper T cells to discrete effector 'lineages' represented a watershed event in conceptualizing mechanisms of host defense and immunoregulation. However, our appreciation for the actual complexity of helper T-cell subsets continues unabated. Just as the Sami language of Scandinavia has 1000 different words for reindeer, immunologists recognize the range of fates available for a CD4+ T cell is numerous and may be underestimated. Added to the crowded scene for helper T-cell subsets is the continuously growing family of innate lymphoid cells (ILCs), endowed with common effector responses and the previously defined 'master regulators' for CD4+ helper T-cell subsets are also shared by ILC subsets. Within the context of this extraordinary complexity are concomitant advances in the understanding of transcriptomes and epigenomes. So what do terms like 'lineage commitment' and helper T-cell 'specification' mean in the early 21st century? How do we put all of this together in a coherent conceptual framework? It would be arrogant to assume that we have a sophisticated enough understanding to seriously answer these questions. Instead, we review the current status of the flexibility of helper T-cell responses in relation to their genetic regulatory networks and epigenetic landscapes. Recent data have provided major surprises as to what master regulators can or cannot do, how they interact with other transcription factors and impact global genome-wide changes, and how all these factors come together to influence helper cell function.

Original languageEnglish (US)
Pages (from-to)23-49
Number of pages27
JournalImmunological reviews
Volume261
Issue number1
DOIs
StatePublished - Sep 2014
Externally publishedYes

Keywords

  • Cell identity
  • Epigenetics
  • Gene regulation
  • ILCs
  • T cells
  • Transcription factors

ASJC Scopus subject areas

  • Immunology and Allergy
  • Immunology

Fingerprint

Dive into the research topics of 'Transcriptional and epigenetic networks of helper T and innate lymphoid cells'. Together they form a unique fingerprint.

Cite this