Patterning definitive hematopoietic stem cells from embryonic stem cells

被引:15
作者
Lengerke, C
Daley, GQ
机构
[1] Childrens Hosp, Div Pediat Hematol Oncol, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Harvard Stem Cell Inst, Boston, MA 02115 USA
[4] Brigham & Womens Hosp, Div Hematol, Boston, MA 02115 USA
[5] Univ Tubingen, Med Ctr 2, Dept Hematol & Oncol, Tubingen, Germany
关键词
D O I
10.1016/j.exphem.2005.06.004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Derived from the inner cell mass of blastocysts, embryonic stem cells (ESCs) retain the pluripotent features of early embryonic epiblast cells. In vitro, ESCs undergo spontaneous differentiation into a multitude of tissues, and thus are a powerful tool for the study of early developmental processes and a promising resource for cell-based therapies. We have pursued the derivation of functional, multipotent and engraftable hematopoietic stem cells (HSCs) from ESCs in order to investigate the genetic pathways specifying blood formation, as well as to lay the foundation for hematopoietic cell replacement therapies based on engineered ESCs. Theoretically, the generation of HSCs from patient-specific ESCs derived by nuclear transfer could provide for autologous hematopoietic therapies for the treatment of malignant and genetic bone marrow disorders. Although significant progress has been made in achieving hematopoietic differentiation from both murine and human ESCs, we have only a primitive understanding of the underlying mechanisms that specify hematopoietic cell fate, and a very limited capacity to direct the differentiation of the definitive HSC that would be suitable for clinical engraftment studies. Here we will review the progress to date and the significant problems that remain, and outline a strategy to achieve the directed differentiation of HSCs under conditions that might be appropriate for clinical scale-up and disease applications. (c) 2005 International Society for Experimental Hematology. Published by Elsevier Inc.
引用
收藏
页码:971 / 979
页数:9
相关论文
共 100 条
[61]   DEVELOPMENT OF HEMATOPOIETIC STEM-CELL ACTIVITY IN THE MOUSE EMBRYO [J].
MULLER, AM ;
MEDVINSKY, A ;
STROUBOULIS, J ;
GROSVELD, F ;
DZIERZAK, E .
IMMUNITY, 1994, 1 (04) :291-301
[62]   GENERATION OF LYMPHOHEMATOPOIETIC CELLS FROM EMBRYONIC STEM-CELLS IN CULTURE [J].
NAKANO, T ;
KODAMA, H ;
HONJO, T .
SCIENCE, 1994, 265 (5175) :1098-1101
[63]  
Nishikawa S, 1998, DEVELOPMENT, V125, P1747
[64]   In vitro generation of lymphohematopoietic cells from endothelial cells purified from murine embryos [J].
Nishikawa, S ;
Nishikawa, S ;
Kawamoto, H ;
Yoshida, H ;
Kizumoto, M ;
Kataoka, H ;
Katsura, Y .
IMMUNITY, 1998, 8 (06) :761-769
[65]   Runx1 expression marks long-term repopulating hematopoietic stem cells in the midgestation mouse embryo [J].
North, TE ;
de Bruijin, MFTR ;
Stacy, T ;
Talebian, L ;
Lind, E ;
Robin, C ;
Binder, M ;
Dzierzak, E ;
Speck, NA .
IMMUNITY, 2002, 16 (05) :661-672
[66]   IN-VITRO GENERATION OF HEMATOPOIETIC STEM-CELLS FROM AN EMBRYONIC STEM-CELL LINE [J].
PALACIOS, R ;
GOLUNSKI, E ;
SAMARIDIS, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (16) :7530-7534
[67]   Opposite phenotypes of hypomorphic and Y766 phosphorylation site mutations reveal a function for Fgfr1 in anteroposterior patterning of mouse embryos [J].
Partanen, J ;
Schwartz, L ;
Rossant, J .
GENES & DEVELOPMENT, 1998, 12 (15) :2332-2344
[68]  
Perlingeiro RCR, 2001, DEVELOPMENT, V128, P4597
[69]   Autocrine and paracrine effects of an ES-cell derived, BCR/ABL-transformed hematopoietic cell line that induces leukemia in mice [J].
Peters, DG ;
Klucher, KM ;
Perlingeiro, RCR ;
Dessain, SK ;
Koh, EY ;
Daley, GQ .
ONCOGENE, 2001, 20 (21) :2636-2646
[70]   The T cell leukemia oncoprotein SCL/tal-1 is essential for development of all hematopoietic lineages [J].
Porcher, C ;
Swat, W ;
Rockwell, K ;
Fujiwara, Y ;
Alt, FW ;
Orkin, SH .
CELL, 1996, 86 (01) :47-57