共 127 条
Critical roles of Bcl11b in T-cell development and maintenance of T-cell identity
被引:84
作者:

Liu, Pentao
论文数: 0 引用数: 0
h-index: 0
机构:
Wellcome Trust Sanger Inst, Cambridge CB10 1HH, England Wellcome Trust Sanger Inst, Cambridge CB10 1HH, England

Li, Peng
论文数: 0 引用数: 0
h-index: 0
机构:
Wellcome Trust Sanger Inst, Cambridge CB10 1HH, England Wellcome Trust Sanger Inst, Cambridge CB10 1HH, England

Burke, Shannon
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机构:
Wellcome Trust Sanger Inst, Cambridge CB10 1HH, England Wellcome Trust Sanger Inst, Cambridge CB10 1HH, England
机构:
[1] Wellcome Trust Sanger Inst, Cambridge CB10 1HH, England
关键词:
Bcl11b;
T cells;
transcription factor;
identity;
natural killer;
reprogramming;
immunotherapy;
NATURAL-KILLER-CELLS;
ACUTE LYMPHOBLASTIC-LEUKEMIA;
TRANSCRIPTION FACTOR BCL11B;
MOUSE THYMIC LYMPHOMAS;
ZINC-FINGER PROTEIN;
HELIX INHIBITOR ID2;
IN-VIVO;
GENE-EXPRESSION;
ALPHA-BETA;
THYMOCYTE DEVELOPMENT;
D O I:
10.1111/j.1600-065X.2010.00953.x
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
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.
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页码:138 / 149
页数:12
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