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Flk2+ common lymphoid progenitors possess equivalent differentiation potential for the B and T lineages
被引:117
作者:
Karsunky, Holger
[1
,2
]
Inlay, Matthew A.
[1
,2
]
Serwold, Thomas
[1
,2
]
Bhattacharya, Deepta
[1
,2
]
Weissman, Irving L.
[1
,2
]
机构:
[1] Stanford Univ, Inst Stem Cell Biol & Regenerat Med, Dept Pathol, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Dev Biol, Stanford, CA 94305 USA
来源:
关键词:
D O I:
10.1182/blood-2007-11-126219
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Mature blood cells develop from multipotent hematopoietic stem cells through a series of sequential intermediates in which the developmental potential for particular blood lineages is progressively extinguished. We previously reported the identification of one of these developmental intermediates, the common lymphoid progenitor (CLIP), which can give rise to T cells, B cells, dendritic cells (DCs), and natural killer cells (NKs), but lacks myeloid and erythroid potential. Recently, several studies have suggested that the T-cell and DC potential of CLP is limited or absent, and/or that CLP contains significant myeloid potential. Here, we show that the originally identified CLIP population can be divided into functionally distinct subsets based on the expression of the tyrosine kinase receptor, Flk2. The Flk2(+) subset contains robust in vivo and in vitro T-cell, B-cell, DC, and NK potential, but lacks myeloid potential and, therefore, represents an oligopotent, lymphoid-restricted progenitor. This population of cells does not appear to be B cell-biased and robustly reconstitutes both B and T lineages in vivo, consistent with its being a physiologic progenitor of both of these subsets. Thus, Flk2 expression defines a homogeneous, readily obtainable subset of bone marrow CLP that is completely lymphoid-committed and can differentiate equivalently well into both B and T lineages.
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页码:5562 / 5570
页数:9
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