Reprogramming of T cells to natural killer-like cells upon Bcl11b deletion

Science. 2010 Jul 2;329(5987):85-9. doi: 10.1126/science.1188063. Epub 2010 Jun 10.

Abstract

T cells develop in the thymus and are critical for adaptive immunity. Natural killer (NK) lymphocytes constitute an essential component of the innate immune system in tumor surveillance, reproduction, and defense against microbes and viruses. Here, we show that the transcription factor Bcl11b was expressed in all T cell compartments and was indispensable for T lineage development. When Bcl11b was deleted, T cells from all developmental stages acquired NK cell properties and concomitantly lost or decreased T cell-associated gene expression. These induced T-to-natural killer (ITNK) cells, which were morphologically and genetically similar to conventional NK cells, killed tumor cells in vitro, and effectively prevented tumor metastasis in vivo. Therefore, ITNKs may represent a new cell source for cell-based therapies.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Cell Lineage*
  • Cells, Cultured
  • Coculture Techniques
  • Cytotoxicity, Immunologic
  • Gene Deletion
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental
  • Gene Knock-In Techniques
  • Genes, T-Cell Receptor beta
  • Killer Cells, Natural / cytology
  • Killer Cells, Natural / immunology
  • Killer Cells, Natural / physiology*
  • Lymphopoiesis* / genetics
  • Melanoma, Experimental / immunology
  • Melanoma, Experimental / therapy
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Oligonucleotide Array Sequence Analysis
  • Precursor Cells, T-Lymphoid / cytology
  • Precursor Cells, T-Lymphoid / physiology
  • Receptors, Antigen, T-Cell, alpha-beta / metabolism
  • Repressor Proteins / genetics*
  • Repressor Proteins / metabolism*
  • Signal Transduction
  • Stromal Cells / cytology
  • Stromal Cells / physiology
  • T-Lymphocytes / cytology
  • T-Lymphocytes / immunology
  • T-Lymphocytes / physiology*
  • T-Lymphocytes / transplantation
  • Tamoxifen / analogs & derivatives
  • Tamoxifen / pharmacology
  • Tumor Suppressor Proteins / genetics*
  • Tumor Suppressor Proteins / metabolism*

Substances

  • Bcl11b protein, mouse
  • Receptors, Antigen, T-Cell, alpha-beta
  • Repressor Proteins
  • Tumor Suppressor Proteins
  • Tamoxifen
  • afimoxifene

Associated data

  • GEO/GSE21016