Engineering Hematopoietic Stem Cells: Lessons from Development

被引:69
作者
Rowe, R. Grant [1 ,2 ]
Mandelbaum, Joseph [1 ,2 ]
Zon, Leonard I. [1 ,2 ,3 ,4 ,5 ,6 ]
Daley, George Q. [1 ,2 ,3 ,6 ,7 ,8 ,9 ]
机构
[1] Boston Childrens Hosp, Stem Cell Program, Boston, MA 02115 USA
[2] Boston Childrens Hosp, Div Hematol Oncol, Boston, MA 02115 USA
[3] Howard Hughes Med Inst, Boston, MA 02115 USA
[4] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[5] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[6] Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[7] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[8] Brigham & Womens Hosp, Div Hematol, Boston, MA 02115 USA
[9] Manton Ctr Orphan Dis Res, Boston, MA 02115 USA
关键词
GENOME-WIDE ASSOCIATION; VERSUS-HOST-DISEASE; DEFINITIVE HEMATOPOIESIS; YOLK-SAC; SELF-RENEWAL; BONE-MARROW; LINEAGE COMMITMENT; ENDOTHELIAL-CELLS; BLOOD-CELLS; IN-VITRO;
D O I
10.1016/j.stem.2016.05.016
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Cell engineering has brought us tantalizingly close to the goal of deriving patient-specific hematopoietic stem cells (HSCs). While directed differentiation and transcription factor-mediated conversion strategies have generated progenitor cells with multilineage potential, to date, therapy-grade engineered HSCs remain elusive due to insufficient long-term self-renewal and inadequate differentiated progeny functionality. A cross-species approach involving zebrafish and mammalian systems offers complementary methodologies to improve understanding of native HSCs. Here, we discuss the role of conserved developmental timing processes in vertebrate hematopoiesis, highlighting how identification and manipulation of stage-specific factors that specify HSC developmental state must be harnessed to engineer HSCs for therapy.
引用
收藏
页码:707 / 720
页数:14
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