A robust and highly efficient immune cell reprogramming system

Cell Stem Cell. 2009 Nov 6;5(5):554-66. doi: 10.1016/j.stem.2009.10.004.

Abstract

Here we describe a lineage reprogramming system consisting of a B cell line with an estradiol-inducible form of C/EBPalpha where cells can be converted into macrophage-like cells at 100% efficiency within 2 to 3 days. The reprogrammed cells are larger, contain altered organelle and cytoskeletal structures, are phagocytic, and exhibit an inflammatory response. Time-lapse experiments showed that the cells acquire a macrophage morphology and increased migratory activity as early as 10 hr. During induction, thousands of genes become up- or downregulated, including several dozen transcription and chromatin-remodeling factors. Time-limited exposure of cells to the inducer showed that the reprogrammed cells become transgene independent within 1 to 2 days. The reprogramming can be inhibited, at least partially, by perturbation experiments with B cell and macrophage transcription factors. The tightness, robustness, and speed of the system described make it a versatile tool to study biochemical and biological aspects of lineage reprogramming.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Differentiation / metabolism
  • Basic-Leucine Zipper Transcription Factors / genetics
  • Basic-Leucine Zipper Transcription Factors / metabolism*
  • Cell Line, Transformed
  • Cell Movement / genetics
  • Cell Movement / immunology
  • Cell Transdifferentiation*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Estradiol / metabolism
  • Estrogen Receptor alpha / genetics
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental / immunology
  • Inflammation Mediators / metabolism
  • Macrophages / cytology
  • Macrophages / immunology
  • Macrophages / metabolism*
  • Mice
  • Precursor Cells, B-Lymphoid / cytology
  • Precursor Cells, B-Lymphoid / immunology
  • Precursor Cells, B-Lymphoid / metabolism*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism*
  • Transcription Factor AP-2
  • Transcriptional Activation
  • Transduction, Genetic

Substances

  • Antigens, Differentiation
  • Basic-Leucine Zipper Transcription Factors
  • DNA-Binding Proteins
  • Estrogen Receptor alpha
  • Inflammation Mediators
  • Recombinant Fusion Proteins
  • Tfap2a protein, mouse
  • Transcription Factor AP-2
  • Estradiol

Associated data

  • GEO/GSE17316