Cell lineage tracing during Xenopus tail regeneration
- PMID: 15148301
- DOI: 10.1242/dev.01155
Cell lineage tracing during Xenopus tail regeneration
Abstract
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.
Similar articles
-
Cellular and molecular mechanisms of regeneration in Xenopus.Philos Trans R Soc Lond B Biol Sci. 2004 May 29;359(1445):745-51. doi: 10.1098/rstb.2004.1463. Philos Trans R Soc Lond B Biol Sci. 2004. PMID: 15293801 Free PMC article. Review.
-
Tail regeneration in the Xenopus tadpole.Dev Growth Differ. 2007 Feb;49(2):155-61. doi: 10.1111/j.1440-169X.2007.00912.x. Dev Growth Differ. 2007. PMID: 17335436 Review.
-
Spinal cord is required for proper regeneration of the tail in Xenopus tadpoles.Dev Growth Differ. 2008 Feb;50(2):109-20. doi: 10.1111/j.1440-169X.2007.00981.x. Dev Growth Differ. 2008. PMID: 18211586
-
Cornea-lens transdifferentiation in the anuran, Xenopus tropicalis.Dev Genes Evol. 2001 Sep;211(8-9):377-87. doi: 10.1007/s004270100163. Dev Genes Evol. 2001. PMID: 11685571
-
Ectoderm to mesoderm lineage switching during axolotl tail regeneration.Science. 2002 Dec 6;298(5600):1993-6. doi: 10.1126/science.1077804. Science. 2002. PMID: 12471259
Cited by
-
Specialized progenitors and regeneration.Development. 2013 Mar;140(5):951-7. doi: 10.1242/dev.080499. Development. 2013. PMID: 23404104 Free PMC article. Review.
-
Finding Solutions for Fibrosis: Understanding the Innate Mechanisms Used by Super-Regenerator Vertebrates to Combat Scarring.Adv Sci (Weinh). 2021 Aug;8(15):e2100407. doi: 10.1002/advs.202100407. Epub 2021 May 24. Adv Sci (Weinh). 2021. PMID: 34032013 Free PMC article. Review.
-
Differential muscle regulatory factor gene expression between larval and adult myogenesis in the frog Xenopus laevis: adult myogenic cell-specific myf5 upregulation and its relation to the notochord suppression of adult muscle differentiation.In Vitro Cell Dev Biol Anim. 2013 Aug;49(7):524-36. doi: 10.1007/s11626-013-9635-z. Epub 2013 May 25. In Vitro Cell Dev Biol Anim. 2013. PMID: 23708921
-
Musashi and Plasticity of Xenopus and Axolotl Spinal Cord Ependymal Cells.Front Cell Neurosci. 2018 Feb 27;12:45. doi: 10.3389/fncel.2018.00045. eCollection 2018. Front Cell Neurosci. 2018. PMID: 29535610 Free PMC article.
-
To regenerate or not to regenerate: Vertebrate model organisms of regeneration-competency and -incompetency.Wound Repair Regen. 2022 Nov;30(6):623-635. doi: 10.1111/wrr.13000. Epub 2022 Feb 22. Wound Repair Regen. 2022. PMID: 35192230 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources