Beyond Early Development: Xenopus as an Emerging Model for the Study of Regenerative Mechanisms

被引:126
作者
Beck, Caroline W. [1 ]
Izpisua Belmonte, Juan Carlos [2 ,3 ]
Christen, Bea [2 ]
机构
[1] Univ Otago, Dept Zool & Genet Otago, Dunedin 9064, New Zealand
[2] Ctr Regenerat Med Barcelona, Barcelona, Spain
[3] Salk Inst Biol Studies, Gene Express Lab, La Jolla, CA 92037 USA
关键词
Xenopus; regeneration; blastema; epimorphic; transdifferentiation; tail; limb; lens; transcriptome; Hsp70; FIBROBLAST-GROWTH-FACTOR; CORNEA-LENS TRANSDIFFERENTIATION; ZEBRAFISH FIN REGENERATION; AXOLOTL TAIL REGENERATION; MESSENGER-RNA EXPRESSION; I-SCEI MEGANUCLEASE; CHICK LIMB-BUD; GENE-EXPRESSION; SPINAL-CORD; OUTER CORNEA;
D O I
10.1002/dvdy.21890
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100123 [人体微生态学]; 100210 [外科学];
摘要
While Xenopus is a well-known model system for early vertebrate development, in recent years, it has also emerged as a leading model for regeneration research. As an anuran amphibian, Xenopus laevis can regenerate the larval tail and limb by means of the formation of a proliferating blastema, the lens of the eye by transdifferentiation of nearby tissues, and also exhibits a partial regeneration of the postmetamorphic froglet forelimb. With the availability of inducible transgenic techniques for Xenopus, recent experiments are beginning to address the functional role of genes in the process of regeneration. The use of soluble inhibitors has also been very successful in this model. Using the more traditional advantages of Xenopus, others are providing important lineage data on the origin of the cells that make up the tissues of the regenerate. Finally, transcriptome analyses of regenerating tissues seek to identify the genes and cellular processes that enable successful regeneration. Developmental Dynamics 238:1226-1248, 2009. (C) 2009 Wiley-Liss, Inc.
引用
收藏
页码:1226 / 1248
页数:23
相关论文
共 173 条
[1]
H+ pump-dependent changes in membrane voltage are an early mechanism necessary and sufficient to induce Xenopus tail regeneration [J].
Adams, Dany S. ;
Masi, Alessio ;
Levin, Michael .
DEVELOPMENT, 2007, 134 (07) :1323-1335
[2]
Inverse drug screens: A rapid and inexpensive method for implicating molecular targets [J].
Adams, Dany S. ;
Levin, Michael .
GENESIS, 2006, 44 (11) :530-540
[3]
ALBERCH P, 1983, J EMBRYOL EXP MORPH, V76, P177
[4]
[Anonymous], 1994, Normal Table of Xenopus laevis (Daudin): A Systematical and Chronological Survey of the Development from the Fertilized Egg till the End of Metamorphosis
[5]
[Anonymous], MIRBASE
[6]
Lens-forming competence in the epidermis of Xenopus laevis during development [J].
Arresta, E ;
Bernardini, S ;
Gargioli, C ;
Filoni, S ;
Cannata, SM .
JOURNAL OF EXPERIMENTAL ZOOLOGY PART A-ECOLOGICAL AND INTEGRATIVE PHYSIOLOGY, 2005, 303A (01) :1-12
[7]
BARKER DM, 2009, DEV DYN IN PRESS
[8]
Gut specific expression using mammalian promoters in transgenic Xenopus laevis [J].
Beck, CW ;
Slack, JMW .
MECHANISMS OF DEVELOPMENT, 1999, 88 (02) :221-227
[9]
Molecular pathways needed for regeneration of spinal cord and muscle in a vertebrate [J].
Beck, CW ;
Christen, B ;
Slack, JMW .
DEVELOPMENTAL CELL, 2003, 5 (03) :429-439
[10]
Beck CW, 2002, INT J DEV BIOL, V46, P255