Elucidation of the phenotypic, functional, and molecular topography of a myeloerythroid progenitor cell hierarchy

被引:489
作者
Pronk, Cornelis J. H.
Rossi, Derrick J.
Mansson, Robert
Attema, Joanne L.
Norddahl, Gudmundur Logi
Chan, Charles Kwok Fai
Sigvardsson, Mikael
Weissman, Irving L.
Bryder, David
机构
[1] Lund Univ, Lund Strateg Res Ctr Stem Cell Biol & Cell Therap, S-22184 Lund, Sweden
[2] Lund Univ, Immunol Unit, Inst Expt Med Sci, S-22184 Lund, Sweden
[3] Stanford Univ, Sch Med, Dept Pathol, Stanford, CA 94305 USA
[4] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
[5] Stanford Univ, Sch Med, Inst Stem Cell Biol & Regenerat Med, Stanford, CA 94305 USA
关键词
D O I
10.1016/j.stem.2007.07.005
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The major myeloid blood cell lineages are generated from hematopoietic stem cells by differentiation through a series of increasingly committed progenitor cells. Precise characterization of intermediate progenitors is important for understanding fundamental differentiation processes and a variety of disease states, including leukemia. Here, we evaluated the functional in vitro and in vivo potentials of a range of prospectively isolated myeloid precursors with differential expression of CD150, Endoglin, and CD41. Our studies revealed a hierarchy of myeloerythroid progenitors with distinct lineage potentials. The global gene expression signatures of these subsets were consistent with their functional capacities, and hierarchical clustering analysis suggested likely lineage relationships. These studies provide valuable tools for understanding myeloid lineage commitment, including isolation of an early erythroid-restricted precursor, and add to existing models of hematopoietic differentiation by suggesting that progenitors of the innate and adaptive immune system can separate late, following the divergence of megakaryocytic/erythroid potential.
引用
收藏
页码:428 / 442
页数:15
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