Human embryonic stem cells as a cellular model for human disorders

被引:30
作者
Ben-Nun, Inbar Friedrich [1 ]
Benvenisty, Nissim [1 ]
机构
[1] Hebrew Univ Jerusalem, Inst Life Sci, Dept Genet, IL-91904 Jerusalem, Israel
关键词
human embryonic stem cells; genetic diseases; human disorders; nuclear transfer; preimplantation genetic diagnosis; genetic manipulation; gene trap;
D O I
10.1016/j.mce.2006.03.034
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Human embryonic stem cells (HESCs) are pluripotent cell lines derived from the inner cell mass (ICM) of embryos at the blastocyst stage. These cells possess self renewal capacity and differentiation potential to all three embryonic germ layers. These unique characters made HESCs an attractive research tool for studying early human developmental processes as well as a potential therapeutic tool for various human diseases. Here, we focus on HESCs as a cellular model for human disorders: The advantages of such models as well as the various methodologies to achieve HESCs carrying a genetic defect will be discussed. (c) 2006 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:154 / 159
页数:6
相关论文
共 37 条
[1]   RNA interference: Biology, mechanism, and applications [J].
Agrawal, N ;
Dasaradhi, PVN ;
Mohmmed, A ;
Malhotra, P ;
Bhatnagar, RK ;
Mukherjee, SK .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 2003, 67 (04) :657-+
[2]   Atm-deficient mice: A paradigm of ataxia telangiectasia [J].
Barlow, C ;
Hirotsune, S ;
Paylor, R ;
Liyanage, M ;
Eckhaus, M ;
Collins, F ;
Shiloh, Y ;
Crawley, JN ;
Ried, T ;
Tagle, D ;
WynshawBoris, A .
CELL, 1996, 86 (01) :159-171
[3]   Mouse models of human disease .2. Recent progress and future directions [J].
Bedell, MA ;
Largaespada, DA ;
Jenkins, NA ;
Copeland, NG .
GENES & DEVELOPMENT, 1997, 11 (01) :11-43
[4]   Preimplantation genetic diagnosis [J].
Braude, P ;
Pickering, S ;
Flinter, F ;
Ogilvie, CM .
NATURE REVIEWS GENETICS, 2002, 3 (12) :941-953
[5]   Bypass of senescence after disruption of p21(CIP1/WAF1) gene in normal diploid human fibroblasts [J].
Brown, JP ;
Wei, WY ;
Sedivy, JM .
SCIENCE, 1997, 277 (5327) :831-834
[6]   Requirement for p53 and p21 to sustain G2 arrest after DNA damage [J].
Bunz, F ;
Dutriaux, A ;
Lengauer, C ;
Waldman, T ;
Zhou, S ;
Brown, JP ;
Sedivy, JM ;
Kinzler, KW ;
Vogelstein, B .
SCIENCE, 1998, 282 (5393) :1497-1501
[7]   Gene trap as a tool for genome annotation and analysis of X chromosome inactivation in human embryonic stem cells [J].
Dhara, SK ;
Benvenisty, N .
NUCLEIC ACIDS RESEARCH, 2004, 32 (13) :3995-4002
[8]   Embryonic stem cells: a promising tool for cell replacement therapy [J].
Doss, MX ;
Koehler, CI ;
Gissel, C ;
Hescheler, J ;
Sachinidis, A .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (04) :465-473
[9]   Human embryonic stem cells as a model for early human development [J].
Dvash, T ;
Benvenisty, N .
BEST PRACTICE & RESEARCH CLINICAL OBSTETRICS & GYNAECOLOGY, 2004, 18 (06) :929-940
[10]   Establishment of human embryonic stem cell-transfected clones carrying a marker for undifferentiated cells [J].
Eiges, R ;
Schuldiner, M ;
Drukker, M ;
Yanuka, O ;
Itskovitz-Eldor, J ;
Benvenisty, N .
CURRENT BIOLOGY, 2001, 11 (07) :514-518