Critical roles of Bcl11b in T-cell development and maintenance of T-cell identity

Immunol Rev. 2010 Nov;238(1):138-49. doi: 10.1111/j.1600-065X.2010.00953.x.

Abstract

T-cell development primarily occurs in the thymus and involves in the interactions of many important transcription factors. Until recently, no single transcription factor has been identified to be essential for T-cell lineage commitment or maintenance of T-cell identity. Recent studies have now identified the zinc finger transcription factor Bcl11b to be essential for T-cell development and for maintenance of T-cell identity. Remarkably, T cells acquire NK cell properties upon Bcl11b deletion. These reprogrammed cells have unique properties in proliferation, cytokine dependency and killing target cells, and may therefore provide a new cell source for some cell-based therapies.

Publication types

  • Review

MeSH terms

  • Animals
  • Cell Differentiation / immunology
  • Cell Lineage
  • Cell Transdifferentiation* / genetics
  • Cell Transdifferentiation* / immunology
  • Humans
  • Immunotherapy*
  • Killer Cells, Natural / immunology*
  • Repressor Proteins / genetics
  • Repressor Proteins / immunology*
  • Sequence Deletion / genetics
  • T-Lymphocytes / immunology*
  • Tumor Suppressor Proteins / genetics
  • Tumor Suppressor Proteins / immunology*

Substances

  • BCL11B protein, human
  • Repressor Proteins
  • Tumor Suppressor Proteins