A Robust and Highly Efficient Immune Cell Reprogramming System

被引:115
作者
Bussmann, Lars H. [1 ,2 ]
Schubert, Alexis [1 ,2 ]
Vu Manh, Thien Phong [1 ,2 ]
De Andres, Luisa [1 ,2 ]
Desbordes, Sabrina C. [1 ,2 ,3 ]
Parra, Maribel [1 ,2 ]
Zimmermann, Timo [1 ,2 ]
Rapino, Francesca [1 ,2 ]
Rodriguez-Ubreva, Javier [3 ]
Ballestar, Esteban [3 ]
Graf, Thomas [1 ,2 ,4 ]
机构
[1] Ctr Genom Regulat, Barcelona 08003, Spain
[2] Univ Pompeu Fabra, Barcelona 08003, Spain
[3] Bellvitge Inst Biomed Res IDIBELL, Barcelona 08907, Spain
[4] Inst Catalana Recerca & Estudis Avancats, Catalonia, Spain
关键词
C/EBP-ALPHA; IN-VIVO; TRANSCRIPTIONAL CONTROL; RHO-GTPASES; B-CELLS; GENES; PU.1; DIFFERENTIATION; MACROPHAGES; EXPRESSION;
D O I
10.1016/j.stem.2009.10.004
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Here we describe a lineage reprogramming system consisting of a B cell line with an estradiol-inducible form of C/EBP alpha 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.
引用
收藏
页码:554 / 566
页数:13
相关论文
共 42 条
  • [41] Stepwise reprogramming of B cells into macrophages
    Xie, HF
    Ye, M
    Feng, R
    Graf, T
    [J]. CELL, 2004, 117 (05) : 663 - 676
  • [42] Zhou Q, 2008, NATURE, V455, P627, DOI 10.1038/nature07314