Regeneration of Amputated Zebrafish Fin Rays from De Novo Osteoblasts

Developmental Cell

Volumn 22, Issue 4, 2012, Pages 879-886

  Singh, Sumeet Pal ^a   Holdway, Jennifer E ^a   Poss, Kenneth D ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMPUTATION; ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; BONE INJURY; BONE REGENERATION; CELL DEDIFFERENTIATION; CELL POPULATION; CONTROLLED STUDY; EMBRYO; FIN (ORGAN); GENE MAPPING; NONHUMAN; OSTEOBLAST; PRIORITY JOURNAL; SURVIVAL; ZEBRA FISH;

AMPUTATION; ANIMAL FINS; ANIMALS; ANIMALS, GENETICALLY MODIFIED; BONE AND BONES; CELL DIFFERENTIATION; CELL LINEAGE; EXTREMITIES; FLOW CYTOMETRY; GREEN FLUORESCENT PROTEINS; OSTEOBLASTS; REGENERATION; ZEBRAFISH;

AMPHIBIA; ANIMALIA; DANIO RERIO;

EID: 84859845794     PISSN: 15345807     EISSN: 18781551     Source Type: Journal    
DOI: 10.1016/j.devcel.2012.03.006     Document Type: Article

References (38)

1. Akimenko M.A., Johnson S.L., Westerfield M., Ekker M. Differential induction of four msx homeobox genes during fin development and regeneration in zebrafish. Development 1995, 121:347-357.
2. Brockes J.P., Kumar A. Appendage regeneration in adult vertebrates and implications for regenerative medicine. Science 2005, 310:1919-1923.
3. Curado S., Anderson R.M., Jungblut B., Mumm J., Schroeter E., Stainier D.Y. Conditional targeted cell ablation in zebrafish: a new tool for regeneration studies. Dev. Dyn. 2007, 236:1025-1035.
4. Dor Y., Brown J., Martinez O.I., Melton D.A. Adult pancreatic beta-cells are formed by self-duplication rather than stem-cell differentiation. Nature 2004, 429:41-46.
5. Dunis D.A., Namenwirth M. The role of grafted skin in the regeneration of x-irradiated axolotl limbs. Dev. Biol. 1977, 56:97-109.
6. Goss R.J., Stagg M.W. The regeneration of fins and fin rays in Fundulus heteroclitus. J. Exp. Zool. 1957, 136:487-507.
7. Grohmann M., Paulmann N., Fleischhauer S., Vowinckel J., Priller J., Walther D.J. A mammalianized synthetic nitroreductase gene for high-level expression. BMC Cancer 2009, 9:301.
8. Inohaya K., Takano Y., Kudo A. The teleost intervertebral region acts as a growth center of the centrum: in vivo visualization of osteoblasts and their progenitors in transgenic fish. Dev. Dyn. 2007, 236:3031-3046.
9. Johnson S.L., Weston J.A. Temperature-sensitive mutations that cause stage-specific defects in Zebrafish fin regeneration. Genetics 1995, 141:1583-1595.
10. Karsenty G. Transcriptional control of skeletogenesis. Annu. Rev. Genomics Hum. Genet. 2008, 9:183-196.
11. Kikuchi K., Holdway J.E., Werdich A.A., Anderson R.M., Fang Y., Egnaczyk G.F., Evans T., Macrae C.A., Stainier D.Y., Poss K.D. Primary contribution to zebrafish heart regeneration by gata4(+) cardiomyocytes. Nature 2010, 464:601-605.
12. Knopf F., Hammond C., Chekuru A., Kurth T., Hans S., Weber C.W., Mahatma G., Fisher S., Brand M., Schulte-Merker S., Weidinger G. Bone regenerates via dedifferentiation of osteoblasts in the zebrafish fin. Dev. Cell 2011, 20:713-724.
13. Kragl M., Knapp D., Nacu E., Khattak S., Maden M., Epperlein H.H., Tanaka E.M. Cells keep a memory of their tissue origin during axolotl limb regeneration. Nature 2009, 460:60-65.
14. Lee Y., Grill S., Sanchez A., Murphy-Ryan M., Poss K.D. Fgf signaling instructs position-dependent growth rate during zebrafish fin regeneration. Development 2005, 132:5173-5183.
15. Li N., Felber K., Elks P., Croucher P., Roehl H.H. Tracking gene expression during zebrafish osteoblast differentiation. Dev. Dyn. 2009, 238:459-466.
16. Lo D.C., Allen F., Brockes J.P. Reversal of muscle differentiation during urodele limb regeneration. Proc. Natl. Acad. Sci. USA 1993, 90:7230-7234.
17. Morrison J.I., Lööf S., He P., Simon A. Salamander limb regeneration involves the activation of a multipotent skeletal muscle satellite cell population. J. Cell Biol. 2006, 172:433-440.
18. Nabrit S.M. The role of fin rays in the regenreation in the tail-fins of fishes. Biol. Bull. 1929, 56:235-266.
19. Nabrit S.M. The role of the basal plate in regeneration in the tail-fins of fishes. Biol. Bull. 1931, 60:60-63.
20. Namenwirth M. The inheritance of cell differentiation during limb regeneration in the axolotl. Dev. Biol. 1974, 41:42-56.
21. Pisharath H., Rhee J.M., Swanson M.A., Leach S.D., Parsons M.J. Targeted ablation of beta cells in the embryonic zebrafish pancreas using E. coli nitroreductase. Mech. Dev. 2007, 124:218-229.
22. Poss K.D. Advances in understanding tissue regenerative capacity and mechanisms in animals. Nat. Rev. Genet. 2010, 11:710-722.
23. Poss K.D., Wilson L.G., Keating M.T. Heart regeneration in zebrafish. Science 2002, 298:2188-2190.
24. Provost E., Rhee J., Leach S.D. Viral 2A peptides allow expression of multiple proteins from a single ORF in transgenic zebrafish embryos. Genesis 2007, 45:625-629.
25. Renn J., Winkler C. Osterix-mCherry transgenic medaka for in vivo imaging of bone formation. Dev. Dyn. 2009, 238:241-248.
26. Smith A., Avaron F., Guay D., Padhi B.K., Akimenko M.A. Inhibition of BMP signaling during zebrafish fin regeneration disrupts fin growth and scleroblasts differentiation and function. Dev. Biol. 2006, 299:438-454.
27. Sousa S., Afonso N., Bensimon-Brito A., Fonseca M., Simões M., Leon J., Roehl H., Cancela M.L., Jacinto A. Differentiated skeletal cells contribute to blastema formation during zebrafish fin regeneration. Development 2011, 138:3897-3905.
28. Steen T.P. Stability of chondrocyte differentiation and contribution of muscle to cartilage during limb regeneration in the axolotl (Siredon mexicanum). J. Exp. Zool. 1968, 167:49-78.
29. Steen T.P. Origin and differentiative capacities of cells in the blastema of the regenerating salamander limb. Am. Zool. 1970, 10:119-132.
30. Subach O.M., Gundorov I.S., Yoshimura M., Subach F.V., Zhang J., Grüenwald D., Souslova E.A., Chudakov D.M., Verkhusha V.V. Conversion of red fluorescent protein into a bright blue probe. Chem. Biol. 2008, 15:1116-1124.
31. Tanaka E.M., Reddien P.W. The cellular basis for animal regeneration. Dev. Cell 2011, 21:172-185.
32. Thorel F., Népote V., Avril I., Kohno K., Desgraz R., Chera S., Herrera P.L. Conversion of adult pancreatic alpha-cells to beta-cells after extreme beta-cell loss. Nature 2010, 464:1149-1154.
33. Thornton C.S. The histogenesis of the regenerating fore limb of larval Amblystoma after exarticulation of the humerus. J. Morphol. 1938, 62:219-241.
34. Trichas G., Begbie J., Srinivas S. Use of the viral 2A peptide for bicistronic expression in transgenic mice. BMC Biol. 2008, 6:40.
35. Tu S., Johnson S.L. Fate restriction in the growing and regenerating zebrafish fin. Dev. Cell 2011, 20:725-732.
36. Turner C.J. Regeneration of the gonopodium of Gambusia during morphogenesis. J. Exp. Zool. 1941, 87:181-210.
37. Wills A.A., Kidd A.R., Lepilina A., Poss K.D. Fgfs control homeostatic regeneration in adult zebrafish fins. Development 2008, 135:3063-3070.
38. Xu X., D'Hoker J., Stangé G., Bonné S., De Leu N., Xiao X., Van de Casteele M., Mellitzer G., Ling Z., Pipeleers D., et al. Beta cells can be generated from endogenous progenitors in injured adult mouse pancreas. Cell 2008, 132:197-207.