Cell lineage tracing during Xenopus tail regeneration

被引:160
作者
Gargioli, C [1 ]
Slack, JMW [1 ]
机构
[1] Univ Bath, Dept Biol & Biochem, Ctr Regenerat Med, Bath BA2 7AY, Avon, England
来源
DEVELOPMENT | 2004年 / 131卷 / 11期
关键词
Xenopus; tail; regeneration; metaplasia; spinal cord; notochord; muscle; satellite cells; green fluorescent protein; Cre-lox recombination;
D O I
10.1242/dev.01155
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The tail of the Xenopus tadpole will regenerate following amputation, and all three of the main axial structures - the spinal cord, the notochord and the segmented myotomes are found in the regenerated tail. We have investigated the cellular origin of each of these three tissue types during regeneration. We produced Xenopus laevis embryos transgenic for the CMV (Simian Cytomegalovirus) promoter driving GFP (Green Fluorescent Protein) ubiquitously throughout the embryo. Single tissues were then specifically labelled by making grafts at the neurula stage from transgenic donors to unlabelled hosts. When the hosts have developed to tadpoles, they carry a region of the appropriate tissue labelled with GFP. These tails were amputated through the labelled region and the distribution of labelled cells in the regenerate was followed. We also labelled myofibres using the Cre-lox method. The results show that the spinal cord and the notochord regenerate from the same tissue type in the stump, with no labelling of other tissues. In the case of the muscle, we show that the myofibres of the regenerate arise from satellite cells and not from the pre-existing myofibres. This shows that metaplasia between differentiated cell types does not occur, and that the process of Xenopus tail regeneration is more akin to tissue renewal in mammals than to urodele tail regeneration.
引用
收藏
页码:2669 / 2679
页数:11
相关论文
共 36 条
[1]  
Amaya E, 1999, METH MOL B, V97, P393, DOI 10.1385/1-59259-270-8:393
[2]  
ARMAND O, 1983, ARCH ANAT MICROSC MO, V72, P163
[3]  
BAITA SANTA, 1951, ARCH ZOOL ITAL, V36, P105
[4]   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
[5]   Muscle regeneration in amphibians and mammals: Passing the torch [J].
Carlson, BM .
DEVELOPMENTAL DYNAMICS, 2003, 226 (02) :167-181
[6]   Medical perspectives of adults and embryonic stem cells [J].
Cavazzana-Calvo, M ;
André-Schmutz, I ;
Lagresle, C ;
Fischer, A .
COMPTES RENDUS BIOLOGIES, 2002, 325 (10) :1053-1058
[7]  
Cooper RN, 1999, J CELL SCI, V112, P2895
[8]   Skeletal myogenic progenitors originating from embryonic dorsal aorta coexpress endothelial and myogenic markers and contribute to postnatal muscle growth and regeneration [J].
De Angelis, L ;
Berghella, L ;
Coletta, M ;
Lattanzi, L ;
Zanchi, M ;
Cusella-De Angelis, MG ;
Ponzetto, C ;
Cossu, G .
JOURNAL OF CELL BIOLOGY, 1999, 147 (04) :869-877
[9]   Ectoderm to mesoderm lineage switching during axolotl tail regeneration [J].
Echeverri, K ;
Tanaka, EM .
SCIENCE, 2002, 298 (5600) :1993-1996
[10]   In vivo imaging indicates muscle fiber dedifferentiation is a major contributor to the regenerating tail blastema [J].
Echeverri, K ;
Clarke, JDW ;
Tanaka, EM .
DEVELOPMENTAL BIOLOGY, 2001, 236 (01) :151-164