Histone methyltransferase and histone methylation in inflammatory T-cell responses

Immunotherapy. 2013 Sep;5(9):989-1004. doi: 10.2217/imt.13.101.

Abstract

During immune responses, T cells require tightly controlled expression of transcriptional programs to regulate the balance between beneficial and harmful immunity. These transcriptional programs are critical for the lineage specification of effector T cells, the production of effector cytokines and molecules, and the development and maintenance of memory T cells. An emerging theme is that post-translational modification of histones by methylation plays an important role in orchestrating the expression of transcriptional programs in T cells. In this article, we provide a broad overview of histone methylation signatures for effector molecules and transcription factors in T cells, and the functional importance of histone methyltransferases in regulating T-cell immune responses.

Publication types

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

MeSH terms

  • Animals
  • Gene Expression Regulation, Enzymologic / physiology*
  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase* / biosynthesis
  • Histone-Lysine N-Methyltransferase* / immunology
  • Humans
  • Immunity, Cellular / physiology*
  • Immunologic Memory / physiology*
  • T-Lymphocytes* / enzymology
  • T-Lymphocytes* / immunology
  • Transcription, Genetic / physiology*

Substances

  • Histone Methyltransferases
  • Histone-Lysine N-Methyltransferase