Reprogrammed Cells for Disease Modeling and Regenerative Medicine

被引:100
作者
Cherry, Anne B. C. [1 ,2 ,4 ,6 ]
Daley, George Q. [1 ,2 ,3 ,4 ,5 ,6 ]
机构
[1] Childrens Hosp, Howard Hughes Med Inst, Stem Cell Transplantat Program, Div Pediat Hematol Oncol,Manton Ctr Orphan Dis Re, Boston, MA 02115 USA
[2] Dana Farber Canc Inst, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Div Hematol, Boston, MA 02115 USA
[4] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[5] Broad Inst, Boston, MA 02115 USA
[6] Harvard Stem Cell Inst, Boston, MA 02115 USA
来源
ANNUAL REVIEW OF MEDICINE, VOL 64 | 2013年 / 64卷
关键词
induced pluripotent stem (iPS) cells; history of reprogramming; cellular therapy; gene correction; hematology; PLURIPOTENT STEM-CELLS; HEMATOPOIETIC DIFFERENTIATION; AORTIC ENDOTHELIUM; APLASTIC-ANEMIA; GENE CORRECTION; TRANSPLANTATION; FIBROBLASTS; EXPRESSION; MUTATIONS; GENERATION;
D O I
10.1146/annurev-med-050311-163324
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The conversion of somatic cells into pluripotent cells is transforming the way diseases are researched and treated. Induced pluripotent stem (iPS) cells' promise may soon be realized in the field of hematology, as hematopoietic stem cell transplants are already commonplace in clinics around the world. We provide a current comparison between induced pluripotent and embryonic stem cells, describe progress toward modeling hematological disorders using iPS cells, and illustrate the hurdles that must be overcome before iPS cell therapies will be available in clinics.
引用
收藏
页码:277 / 290
页数:14
相关论文
共 67 条
[1]   Nonviable human pre-implantation embryos as a source of stem cells for research and potential therapy [J].
Alikani, Mina ;
Munne, Santiago .
STEM CELL REVIEWS, 2005, 1 (04) :337-343
[2]   Hematopoietic stem cell transplantation for severe aplastic anemia - experience of an institute in Taiwan [J].
Bai, LY ;
Chiou, TJ ;
Liu, JH ;
Yen, CC ;
Wang, WS ;
Yan, MH ;
Hsiao, LT ;
Chao, TC ;
Chen, PM .
ANNALS OF HEMATOLOGY, 2004, 83 (01) :38-43
[3]   The tumorigenicity of human embryonic and induced pluripotent stem cells [J].
Ben-David, Uri ;
Benvenisty, Nissim .
NATURE REVIEWS CANCER, 2011, 11 (04) :268-277
[4]   Haematopoietic stem cells derive directly from aortic endothelium during development [J].
Bertrand, Julien Y. ;
Chi, Neil C. ;
Santoso, Buyung ;
Teng, Shutian ;
Stainier, Didier Y. R. ;
Traver, David .
NATURE, 2010, 464 (7285) :108-U120
[5]   Adult mice generated from induced pluripotent stem cells [J].
Boland, Michael J. ;
Hazen, Jennifer L. ;
Nazor, Kristopher L. ;
Rodriguez, Alberto R. ;
Gifford, Wesley ;
Martin, Greg ;
Kupriyanov, Sergey ;
Baldwin, Kristin K. .
NATURE, 2009, 461 (7260) :91-U94
[6]   HOXB4 overexpression promotes hematopoietic development by human embryonic stem cells [J].
Bowles, Kristian M. ;
Vallier, Ludovic ;
Smith, Joseph R. ;
Alexander, Morgan R. J. ;
Pedersen, Roger A. .
STEM CELLS, 2006, 24 (05) :1359-1369
[7]   Sheep cloned by nuclear transfer from a cultured cell line [J].
Campbell, KHS ;
McWhir, J ;
Ritchie, WA ;
Wilmut, I .
NATURE, 1996, 380 (6569) :64-66
[8]   ALTERING THE GENOME BY HOMOLOGOUS RECOMBINATION [J].
CAPECCHI, MR .
SCIENCE, 1989, 244 (4910) :1288-1292
[9]   Efficient design and assembly of custom TALEN and other TAL effector-based constructs for DNA targeting (vol 39, pg e82, 2011) [J].
Cermak, Tomas ;
Doyle, Erin L. ;
Christian, Michelle ;
Wang, Li ;
Zhang, Yong ;
Schmidt, Clarice ;
Baller, Joshua A. ;
Somia, Nikunj V. ;
Bogdanove, Adam J. ;
Voytas, Daniel F. .
NUCLEIC ACIDS RESEARCH, 2011, 39 (17) :7879-7879
[10]   Runx1 is required for the endothelial to haematopoietic cell transition but not thereafter [J].
Chen, Michael J. ;
Yokomizo, Tomomasa ;
Zeigler, Brandon M. ;
Dzierzak, Elaine ;
Speck, Nancy A. .
NATURE, 2009, 457 (7231) :887-891