Apoptosis is required during early stages of tail regeneration in Xenopus laevis

Developmental Biology

Volumn 301, Issue 1, 2007, Pages 62-69

  Tseng, Ai Sun ^a   Adams, Dany S ^a   Qiu, Dayong ^a   Koustubhan, Punita ^a   Levin, Michael ^a  

^a FORSYTH INSTITUTE   (United States)

Author keywords

Apoptosis; Neuron; Otolith; Regeneration; Tail; Xenopus

Indexed keywords

CASPASE 3;

AMPUTATION; ANIMAL EXPERIMENT; ANIMAL TISSUE; APOPTOSIS; ARTICLE; CELL GROWTH; CELL PROLIFERATION; CONTROLLED STUDY; ENZYME ACTIVITY; ENZYME INHIBITION; LARVAL DEVELOPMENT; NERVE FIBER; NEURAL TUBE; NONHUMAN; OTOLITH; PRIORITY JOURNAL; TAIL; TISSUE REGENERATION; XENOPUS LAEVIS;

XENOPUS LAEVIS;

EID: 33845602214     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ydbio.2006.10.048     Document Type: Article

References (55)

1. Abdel-Karim A.E., Michael M.I., and Anton H.J. Mitotic activity in the blastema and stump tissues of regenerating hind limbs of Xenopus laevis larvae after amputation at ankle level. An autoradiographic study. Folia Morphol. (Praha) 38 (1990) 1-11
2. Bagri A., Cheng H.J., Yaron A., Pleasure S.J., and Tessier-Lavigne M. Stereotyped pruning of long hippocampal axon branches triggered by retraction inducers of the semaphorin family. Cell 113 (2003) 285-299
3. Bastida M.F., Delgado M.D., Wang B., Fallon J.F., Fernandez-Teran M., and Ros M.A. Levels of Gli3 repressor correlate with Bmp4 expression and apoptosis during limb development. Dev. Dyn. 231 (2004) 148-160
4. Beck C.W., Christen B., and Slack J.M. Molecular pathways needed for regeneration of spinal cord and muscle in a vertebrate. Dev. Cell 5 (2003) 429-439
5. Briegleb W., Neubert J., Schatz A., Klein T., and Kruse B. Survey of the vestibulum, and behavior of Xenopus laevis larvae developed during a 7-days space flight. Adv. Space Res. 6 (1986) 151-156
6. Bryant S.V., Fyfe D., and Singer M. The effects of denervation on the ultrastructure of young limb regenerates in the newt, Triturus. Dev. Biol. 24 (1971) 577-595
7. Cadinouche M.Z., Liversage R.A., Muller W., and Tsilfidis C. Molecular cloning of the Notophthalmus viridescens radical fringe cDNA and characterization of its expression during forelimb development and adult forelimb regeneration. Dev. Dyn. 214 (1999) 259-268
8. Chakraborty C., Nandi S.S., Sinha S., and Gera V.K. Zebrafish caspase-3: molecular cloning, characterization, crystallization and phylogenetic analysis. Prot. Peptide Letters 13 (2006) 633-640
9. Deuchar E.M. Regeneration of the tail bud in Xenopus embryos. J. Exp. Zool. 192 (1975) 381-390
10. Dyson S., and Gurdon J.B. The interpretation of position in a morphogen gradient as revealed by occupancy of activin receptors. Cell 93 (1998) 557-568
11. Erdem S., Mendell J.R., and Sahenk Z. Fate of Schwann cells in CMT1A and HNPP: evidence for apoptosis. J. Neuropathol. Exp. Neurol. 57 (1998) 635-642
12. Frankfurt O.S. Decreased stability of DNA in cells treated with alkylating agents. Exp. Cell Res. 191 (1990) 181-185
13. Gardiner D.M., Endo T., and Bryant S.V. The molecular basis of amphibian limb regeneration: integrating the old with the new. Semin. Cell Dev. Biol. 13 (2002) 345-352
14. Gargioli C., and Slack J.M. Cell lineage tracing during Xenopus tail regeneration. Development 131 (2004) 2669-2679
15. Goltzene F., Skalski M., Wolff C.M., Meyer D., Mager-Heckel A.M., Darribere T., and Remy P. Heterotopic expression of the Xl-Fli transcription factor during Xenopus embryogenesis: modification of cell adhesion and engagement in the apoptotic pathway. Exp. Cell Res. 260 (2000) 233-247
16. Graham A., Koentges G., and Lumsden A. Neural crest apoptosis and the establishment of craniofacial pattern: an honorable death. Mol. Cell. Neurosci. 8 (1996) 76-83
17. Green J. Morphogen gradients, positional information, and Xenopus: interplay of theory and experiment. Dev. Dyn. 225 (2002) 392-408
18. Guha U., Gomes W.A., Kobayashi T., Pestell R.G., and Kessler J.A. In vivo evidence that BMP signaling is necessary for apoptosis in the mouse limb. Dev. Biol. 249 (2002) 108-120
19. Hirsch S., and Bahr M. Growth promoting and inhibitory effects of glial cells in the mammalian nervous system. Adv. Exp. Med. Biol. 468 (1999) 199-205
20. Honig L.S., and Rosenberg R.N. Apoptosis and neurologic disease. Am. J. Med. 108 (2000) 317-330
21. Huguet C., Morrice D.R., Bouali F., Vandenbunder B., Burt D.W., and Abbadie C. Expression of transcription factor c-Rel and apoptosis occurrence in polydactylous and syndactylous limb buds of the talpid3 mutant chick embryo. Apoptosis 4 (1999) 31-38
22. Hwang J.S., Kobayashi C., Agata K., Ikeo K., and Gojobori T. Detection of apoptosis during planarian regeneration by the expression of apoptosis-related genes and TUNEL assay. Gene 333 (2004) 15-25
23. Ishino T., Shirai M., Kunieda T., Sekimizu K., Natori S., and Kubo T. Identification of genes induced in regenerating Xenopus tadpole tails by using the differential display method. Dev. Dyn. 226 (2003) 317-325
24. James T.N. Normal and abnormal consequences of apoptosis in the human heart. From postnatal morphogenesis to paroxysmal arrhythmias. Circulation 90 (1994) 556-573
25. Johnston M.V. Clinical disorders of brain plasticity. Brain Dev. 26 (2004) 73-80
26. Kaneko Y., Matsumoto G., and Hanyu Y. The occurrence of apoptosis during retinal regeneration in adult newts. Brain Res. Dev. Brain Res. 117 (1999) 225-228
27. Kiba T. The role of the autonomic nervous system in liver regeneration and apoptosis-recent developments. Digestion 66 (2002) 79-88
28. Lademann U., Cain K., Gyrd-Hansen M., Brown D., Peters D., and Jaattela M. Diarylurea compounds inhibit caspase activation by preventing the formation of the active 700-kilodalton apoptosome complex. Mol. Cell. Biol. 23 (2003) 7829-7837
29. Makino S., Whitehead G.G., Lien C.L., Kim S., Jhawar P., Kono A., Kawata Y., and Keating M.T. Heat-shock protein 60 is required for blastema formation and maintenance during regeneration. Proc. Natl. Acad. Sci. U. S. A. 102 (2005) 14599-14604
30. Mallat M., Marin-Teva J.L., and Cheret C. Phagocytosis in the developing CNS: more than clearing the corpses. Curr. Opin. Neurobiol. 15 (2005) 101-107
31. McDiarmid R.W., and Altig R. Tadpoles: The Biology of Anuran Larvae (1999), University of Chicago Press, Chicago, IIL
32. McDowell N., and Gurdon J.B. Activin as a morphogen in Xenopus mesoderm induction. Semin. Cell Dev. Biol. 10 (1999) 311-317
33. Nagy L., Thomazy V.A., and Davies P.J. A transgenic mouse model for the study of apoptosis during limb development. Cell Death Differ. 5 (1998) 126
34. Nieuwkoop P.D., and Faber J. Normal Table of Xenopus laevis (Daudin) (1967), North-Holland Publishing Company, Amsterdam
35. Offner N., Duval N., Jamrich M., and Durand B. The pro-apoptotic activity of a vertebrate Bar-like homeobox gene plays a key role in patterning the Xenopus neural plate by limiting the number of chordin- and shh-expressing cells. Development 132 (2005) 1807-1818
36. Porter A.G., and Janicke R.U. Emerging roles of caspase-3 in apoptosis. Cell Death Differ. 6 (1999) 99-104
37. Ryffel G.U., Werdien D., Turan G., Gerhards A., Goosses S., and Senkel S. Tagging muscle cell lineages in development and tail regeneration using Cre recombinase in transgenic Xenopus. Nucleic Acids Res. 31 (2003) e44
38. Saka Y., and Smith J.C. Spatial and temporal patterns of cell division during early Xenopus embryogenesis. Dev. Biol. 229 (2001) 307-318
39. Sanchez Alvarado A. The freshwater planarian Schmidtea mediterranea: embryogenesis, stem cells and regeneration. Curr. Opin. Genet. Dev. 13 (2003) 438-444
40. Saunders Jr. J.W. Death in embryonic systems. Science 154 (1966) 604-612
41. Singer M. The influence of the nerve in regeneration of the amphibian extremity. Q. Rev. Biol. 27 (1952) 169-200
42. Singer M., and Ilan J. Nerve-dependent regulation of absolute rates of protein synthesis in newt limb regenerates. Measurement of methionine specific activity in peptidyl-tRNA of the growing polypeptide chain. Dev. Biol. 57 (1977) 174-187
43. Sive H.L., Grainger R.M., and Harland R.M. Early Development of Xenopus laevis (2000), Cold Spring Harbor Laboratory Press, New York
44. Slack J.M., Beck C.W., Gargioli C., and Christen B. Cellular and molecular mechanisms of regeneration in Xenopus. Philos. Trans. R. Soc. Lond., B Biol. Sci. 359 (2004) 745-751
45. Stahelin B.J., Marti U., Solioz M., Zimmermann H., and Reichen J. False positive staining in the TUNEL assay to detect apoptosis in liver and intestine is caused by endogenous nucleases and inhibited by diethyl pyrocarbonate. Mol. Pathol. 51 (1998) 204-208
46. Streeter G.L. Some experiments on the developing ear vesicle of the tadpole with relation to equilibration. J. Exp. Zool. 3 (1906) 543-558
47. Sugiura T., Taniguchi Y., Tazaki A., Ueno N., Watanabe K., and Mochii M. Differential gene expression between the embryonic tail bud and regenerating larval tail in Xenopus laevis. Dev. Growth Differ. 46 (2004) 97-105
48. Suzuki M., Satoh A., Ide H., and Tamura K. Nerve-dependent and-independent events in blastema formation during Xenopus froglet limb regeneration. Dev. Biol. 286 (2005) 361-375
49. Thornton C.S. Amphibian limb regeneration and its relation to nerves. Am. Zool. 10 (1970) 113-118
50. Trindade M., Messenger N., Papin C., Grimmer D., Fairclough L., Tada M., and Smith J.C. Regulation of apoptosis in the Xenopus embryo by Bix3. Development 130 (2003) 4611-4622
51. Tsuda T., Ohmori Y., Muramatsu H., Hosaka Y., Takiguchi K., Saitoh F., Kato K., Nakayama K., Nakamura N., Nagata S., and Mochizuki H. Inhibitory effect of M50054, a novel inhibitor of apoptosis, on anti-Fas-antibody-induced hepatitis and chemotherapy-induced alopecia. Eur. J. Pharmacol. 433 (2001) 37-45
52. Van Stry M., McLaughlin K.A., Ataliotis P., and Symes K. The mitochondrial-apoptotic pathway is triggered in Xenopus mesoderm cells deprived of PDGF receptor signaling during gastrulation. Dev. Biol. 268 (2004) 232-242
53. Xiang S., Pan W., and Kastin A.J. Strategies to create a regenerating environment for the injured spinal cord. Curr. Pharm. Des. 11 (2005) 1267-1277
54. Yang S., Lockwood A., Hollett P., Ford R., and Kao K. Overexpression of a novel Xenopus rel mRNA gene induces tumors in early embryos. J. Biol. Chem. 273 (1998) 13746-13752
55. Yu S.Y., Yoo S.J., Yang L., Zapata C., Srinivasan A., Hay B.A., and Baker N.E. A pathway of signals regulating effector and initiator caspases in the developing Drosophila eye. Development 129 (2002) 3269-3278