Prospects for the Xenopus embryo model in therapeutics technologies

被引:11
作者
Brändli, AW [1 ]
机构
[1] Swiss Fed Inst Technol, Inst Pharmaceut Sci, Dept Chem & Appl Biosci, CH-8093 Zurich, Switzerland
关键词
angiogenesis; drug discovery; genomics; kidney organogenesis; Xenopus;
D O I
10.2533/000942904777677443
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Access to suitable animal models is essential in the field of therapeutics technologies. Recently, lower vertebrates have emerged as attractive low-cost animal models which offer new exciting applications in functional genomics and therapeutics technologies. Amphibian embryos of the genus Xenopus have long served as important models for the study of vertebrate development. Xenopus is evolutionary significantly less distant to humans than fish models, which suggests that experimental findings gained with Xenopus will more accurately predict human biology. Numerous experimental advantages, including external development, large size, identifiable blastomeres, and their ability to withstand extensive surgical intervention and culture in vitro, have favored the use of the Xenopus model in the past. More recently, the introduction of a simple efficient method to disrupt gene functions and the rapid development of genomic resources has further increased the attractiveness of this low-cost, high-throughput model for the analysis of vertebrate gene functions. Using the Xenopus embryo as the primary animal model, our research in the field of therapeutics technologies has focused on the identification and validation of novel drug targets by employing genomic and transcriptomic information in the analysis of the molecular and cellular processes underlying kidney organogenesis and vascular development. Furthermore, our research on signaling pathways controlling cellular differentiation of embryonic tissues provides important insights that may ultimately lead to the development of novel cell-based therapies in regenerative medicine. Finally, we are exploring the possibility of employing the Xenopus embryos in chemical library screens to identify novel chemical modulators of organogenesis.
引用
收藏
页码:694 / 702
页数:9
相关论文
共 73 条
[1]   Stem cells in the kidney [J].
Al-Awqati, Q ;
Oliver, JA .
KIDNEY INTERNATIONAL, 2002, 61 (02) :387-395
[2]   Microarray-based analysis of early development in Xenopus laevis [J].
Altmann, CR ;
Bell, E ;
Sczyrba, A ;
Pun, J ;
Bekiranov, S ;
Gaasterland, T ;
Brivanlou, AH .
DEVELOPMENTAL BIOLOGY, 2001, 236 (01) :64-75
[3]   Frog genetics:: Xenopus tropicalis jumps into the future [J].
Amaya, E ;
Offield, MF ;
Grainger, RM .
TRENDS IN GENETICS, 1998, 14 (07) :253-255
[4]   EXPRESSION OF A DOMINANT NEGATIVE MUTANT OF THE FGF RECEPTOR DISRUPTS MESODERM FORMATION IN XENOPUS EMBRYOS [J].
AMAYA, E ;
MUSCI, TJ ;
KIRSCHNER, MW .
CELL, 1991, 66 (02) :257-270
[5]  
BECK CW, 2001, GENOME BIOL, P2
[6]   The NIEHS Xenopus maternal EST project:: interim analysis of the first 13,879 ESTs from unfertilized eggs [J].
Blackshear, PJ ;
Lai, WS ;
Thorn, JM ;
Kennington, EA ;
Staffa, NG ;
Moore, DT ;
Bouffard, GG ;
Beckstrom-Sternberg, SM ;
Touchman, JW ;
Bonaldo, MD ;
Soares, MB .
GENE, 2001, 267 (01) :71-87
[7]   Nephric lineage specification by Pax2 and Pax8 [J].
Bouchard, M ;
Souabni, A ;
Mandler, M ;
Neubüser, A ;
Busslinger, M .
GENES & DEVELOPMENT, 2002, 16 (22) :2958-2970
[8]  
Brändli AW, 1999, INT J DEV BIOL, V43, P381
[9]   A gene trap approach in Xenopus [J].
Bronchain, OJ ;
Hartley, KO ;
Amaya, E .
CURRENT BIOLOGY, 1999, 9 (20) :1195-1198
[10]   Mechanisms of angiogenesis and arteriogenesis [J].
Carmeliet, P .
NATURE MEDICINE, 2000, 6 (04) :389-395