Human embryonic stem cells as a powerful tool for studying human embryogenesis

被引:38
作者
Dvash, Tamar
Ben-Yosef, Dalit
Eiges, Rachel
机构
[1] Inst Life Sci, Dept Genet, IL-91904 Jerusalem, Israel
[2] Lis Matern Hosp, Tel Aviv Sourasky Med Ctr, Sara Racine Vitro Fertilizat Unit, IL-64239 Tel Aviv, Israel
关键词
D O I
10.1203/01.pdr.0000228349.24676.17
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Human embryonic stem cells (HESC) are pluripotent stem cell lines derived from the inner cell mass (ICM) of human blastocyst-stage embryos. They are characterized by their unlimited capacity to self-renew in culture. In addition, they have a broad developmental potential, as demonstrated by their ability to form practically any cell type in vivo and in vitro. These two features have made HESC extremely important in basic and applied research. In addition, they may serve as a powerful tool for studying human development. HESC can recapitulate embryogenesis by expressing developmentally regulated genes and by activating molecular pathways as they occur in vivo. Moreover, they can be used to analyze the effect of specific mutations on particular developmental events and may enable us to identify critical factors that play a role in the processes of cell commitment, differentiation, and adult cell reprogramming. Thus, modeling human embryogenesis by the use of HESC may allow new insights into developmental processes, which would otherwise be inaccessible for research.
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页码:111 / 117
页数:7
相关论文
共 57 条
[1]   Clonally derived human embryonic stem cell lines maintain pluripotency and proliferative potential for prolonged periods of culture [J].
Amit, M ;
Carpenter, MK ;
Inokuma, MS ;
Chiu, CP ;
Harris, CP ;
Waknitz, MA ;
Itskovitz-Eldor, J ;
Thomson, JA .
DEVELOPMENTAL BIOLOGY, 2000, 227 (02) :271-278
[2]   Insulin production by human embryonic stem cells [J].
Assady, S ;
Maor, G ;
Amit, M ;
Itskovitz-Eldor, J ;
Skorecki, KL ;
Tzukerman, M .
DIABETES, 2001, 50 (08) :1691-1697
[3]   Retinal incorporation and differentiation of neural precursors derived from human embryonic stem cells [J].
Banin, Eyal ;
Obolensky, Alexey ;
Idelson, Maria ;
Hemo, Itzhak ;
Reinhardtz, Etti ;
Pikarsky, Eli ;
Ben-Hur, Tamir ;
Reubinoff, Benjamin .
STEM CELLS, 2006, 24 (02) :246-257
[4]   Transplantation of human embryonic stem cell-derived neural progenitors improves behavioral deficit in Parkinsonian rats [J].
Ben-Hur, T ;
Idelson, M ;
Khaner, H ;
Pera, M ;
Reinhartz, E ;
Itzik, A ;
Reubinoff, BE .
STEM CELLS, 2004, 22 (07) :1246-1255
[5]   In vitro differentiation and in vivo mineralization of osteogenic cells derived from human embryonic stem cells [J].
Bielby, RC ;
Boccaccini, AR ;
Polak, JM ;
Buttery, LDK .
TISSUE ENGINEERING, 2004, 10 (9-10) :1518-1525
[6]   X-chromosome inactivation:: closing in on proteins that bind XistRNA [J].
Brockdorff, N .
TRENDS IN GENETICS, 2002, 18 (07) :352-358
[7]   Enrichment of neurons and neural precursors from human embryonic stem cells [J].
Carpenter, MK ;
Inokuma, MS ;
Denham, J ;
Mujtaba, T ;
Chiu, CP ;
Rao, MS .
EXPERIMENTAL NEUROLOGY, 2001, 172 (02) :383-397
[8]   Transcription factors direct the development and function of pancreatic β cells [J].
Chakrabarti, SK ;
Mirmira, RG .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 2003, 14 (02) :78-84
[9]   Nuclear reprogramming of somatic cells after fusion with human embryonic stem cells [J].
Cowan, CA ;
Atienza, J ;
Melton, DA ;
Eggan, K .
SCIENCE, 2005, 309 (5739) :1369-1373
[10]   Efficient differentiation of human embryonic stem cells to definitive endoderm [J].
D'Amour, KA ;
Agulnick, AD ;
Eliazer, S ;
Kelly, OG ;
Kroon, E ;
Baetge, EE .
NATURE BIOTECHNOLOGY, 2005, 23 (12) :1534-1541