Neural retinal regeneration in the anuran amphibian Xenopus laevis post-metamorphosis: Transdifferentiation of retinal pigmented epithelium regenerates the neural retina

Developmental Biology

Volumn 303, Issue 1, 2007, Pages 45-56

  Yoshii, Chika ^a   Ueda, Yoko ^a   Okamoto, Mitumasa ^b   Araki, Masasuke ^a  

^a NARA WOMEN'S UNIVERSITY   (Japan)

^b NAGOYA UNIVERSITY   (Japan)

Author keywords

BrdU; Lens; Organ culture; Pax6; Regeneration; Retina; RPE65; Xenopus laevis

Indexed keywords

FIBROBLAST GROWTH FACTOR 2;

ANIMAL CELL; ANIMAL CELL CULTURE; ANIMAL TISSUE; ARTICLE; CELL DIFFERENTIATION; CELL REGENERATION; CILIATED EPITHELIUM; CONTROLLED STUDY; IN VITRO STUDY; LENS EPITHELIUM; METAMORPHOSIS; NONHUMAN; PIGMENT CELL; PIGMENT EPITHELIUM; PRIORITY JOURNAL; RETINA NEUROEPITHELIAL LAYER; XENOPUS LAEVIS;

AMPHIBIA; ANIMALIA; SALAMANDRIDAE; XENOPUS LAEVIS;

EID: 33846915136     PISSN: 00121606     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ydbio.2006.11.024     Document Type: Article

References (46)

1. Arresta E., Bernardini S., Bernardini E., Filoni S., and Cannata S.M. Pigmented epithelium to retinal transdifferentiation and Pax6 expression in larval Xenopus laevis. J. Exp. Zool. 303A (2005) 1-10
2. Bosco L. Transdifferentiation of ocular tissues in larval Xenopus laevis. Differentiation 39 (1988) 4-15
3. Bosco L., Filoni S., and Cannata S. Relationship between eye factors and lens-forming transformations in the cornea and pericorneal epidermis of larval Xenopus laevis. J. Exp. Zool. 209 (1979) 261-282
4. Cannata S.M., Bagni C., Bernardini S., Christen B., and Filoni S. Nerve-independence of limb regeneration in larval Xenopus laevis is correlated to the level of FGF-2 mRNA expression in limb tissues. Dev. Biol. 231 (2001) 436-446
5. Cannata S.M., Arresta E., Bernardini S., Gargioli C., and Filoni S. Tissue interactions and lens-forming competence in the outer cornea of larval Xenopus laevis. J. Exp. Zool. Part A Comp. Exp. Biol. 299 (2003) 161-171
6. Cioni C., Filoni S., Aquila C., Bernardini S., and Bosco L. Transdifferentiation of eye tissues in anuran amphibians: analysis of the transdifferentiation capacity of the iris of Xenopus laevis larvae. Differentiation 32 (1986) 215-220
7. Colluci V. Sulla rigenerazione parziale dell' occhio nei Tritoni-istogenesi e sviluppo. Studio sperimentale. Mem. R. Accad. Sci. Ist. Bologna, Ser. 51 (1891) 167-203
8. DelRio-Tsonis K., and Tsonis P.A. Eye regeneration at the molecular age. Dev. Dyn. 226 (2003) 211-224
9. Eguchi G. Transdifferentiation as the basis of eye lens regeneration. In: Ferretti P., and Geraudie J. (Eds). Cellular and Molecular Basis of Regeneration: From Invertebrates to Humans (1998), John Wiley and Sons Inc, Chichester 207-228
10. Filoni S. Experimental aspects of regeneration of central nervous system of the anuran amphibians. In: Benedetti I., Bertolini B., and Capanna E. (Eds). Neurology Today Selected Symposia and Monographs U.Z.I. vol. 7 (1992), Muzzi, Modena 237-250
11. Filoni S., Bosco L., and Cioni C. The role of neural retina in lens regeneration from cornea in larval Xenopus laevis. Acta Embryol. Morphol. Exp. 3 (1982) 15-28
12. Freeman G. Lens regeneration from the cornea in Xenopus laevis. J. Exp. Zool. 154 (1963) 39-65
13. Gagliardino J.J., Gomez Dumm C.L., Bianchi C.E., and Luna G.C. Immunocytochemical detection of bromodeoxyuridine in tissues of the toad Bufo arenarum Hensel. Biotech. Histochem. 68 (1993) 302-304
14. Grigorian E.N., Ivanova I.P., and Poplinskaia V.A. The discovery of a new internal sources of neural retinal regeneration after its detachment in newts. Morphological and quantitative research. Izv. Akad. Nauk. Ser. Biol. 3 (1996) 319-332
15. Gwon A., Gruber L.J., Mantras C., and Cunanan C. Lens regeneration in New Zealand albino rabbits after endocapsular cataract extraction. Invest. Ophthalmol. Visual Sci. 34 (1993) 2124-2129
16. Hasegawa M. Restitution of the eye after removal of the retina and lens in the newt, Triturus Pyrrhogaster. Embryologia 4 (1958) 1-32
17. Henry J.J., and Elkins M.B. Cornea-lens transdifferentiation in the anuran. Xenopus tropicalis. Dev. Genes Evol. 211 (2001) 377-387
18. Hitchcock P.F., Macdonald R.E., VanDeRyt J.T., and Wilson S.W. Antibodies against Pax6 immunostain amacrine and ganglion cells and neuronal progenitors, but not rod precursors, in the normal and regenerating retina of the goldfish. J. Neurobiol. 29 (1996) 399-413
19. Hitchcock P., Ochocinska M., Sieh A., and Otteson D. Persistent and injury-induced neurogenesis in the vertebrate retina. Prog. Retin. Eye Res. 23 (2004) 183-194
20. Ikegami Y., Mitsuda S., and Araki M. Neural cell differentiation from retinal pigment epithelial cells of the newt: an organ culture model for the urodele retinal regeneration. J. Neurobiol. 50 (2002) 209-220
21. Kaneko Y., Matsumoto G., and Hanyu Y. Pax-6 expression during retinal regeneration in the adult newt. Dev. Growth Differ. 41 (1999) 723-729
22. 3H-thymidine and colchicines. J. Exp. Zool. 184 (1973) 185-206
23. Levine R.L. Regeneration of the retina in the adult newt, Triturus cristatus, following surgical division of the eye by a limbal incision. J. Exp. Zool. 192 (1975) 363-380
24. Lombardo F. La rigenerazione della retina neurale negli adulti degli Anfibi anuri. Arch. Ital. Anat. Embriol. LXXIV (1969) 29-47
25. Lopashov G.V., and Sologub A.A. Artificial metaplasia of pigmented epithelium into retina in tadpoles and adult frogs. Embryol. Exp. Morph. 28 (1972) 521-546
26. Mitashov V.I. Retinal regeneration in amphibians. Int. J. Dev. Biol. 41 (1997) 893-905
27. Mitusda S., Yoshii C., Ikegami Y., and Araki M. Tissue interaction between the retinal pigment epithelium and the choroid triggers retinal regeneration of the newt Cynops pyrrhogaster. Dev. Biol. 280 (2005) 122-132
28. Nagy T., and Reh T.A. Inhibition of retinal regeneration in larval Rana by an antibody directed against a laminin-heparan sulfate proteoglycan. Dev. Brain Res. 81 (1994) 131-134
29. Okada T.S. Transdifferentiation (1991), Oxford Univ. Press, New York
30. Okamoto M., Ito M., and Owaribe K. Difference between dorsal and ventral iris in lens producing potency in normal lens regeneration is maintained after dissociation and reaggregation of cells from the adult newt. Cynops pyrrhogaster. Dev. Growth Differ. 40 (1998) 11-18
31. Piperno G., and Fuller M.T. Monoclonal antibodies specific for an acetylated form of Alpha-tubulin recognize the antigen in cilia and flagella from a variety of organisms. J. Cell Biol. 101 (1985) 2085-2094
32. Raymond P.A., and Hitchcock P.F. Retinal regeneration: common principles but diversity of mechanism. Adv. Neurol. 72 (1997) 171-184
33. Reh T.A., and Fisher A.J. Stem cells in the vertebrate retina. Brain Behav. Evol. 58 (2001) 296-305
34. Reh T.A., and Nagy T. A possible role for the vascular membrane in retinal regeneration in Rana catesbienna tadpoles. Dev. Biol. 122 (1987) 471-482
35. Reyer R.W. The origins of the regenerating neural retina in two species of Urodele. Anat. Rec. 169 (1971) 410-411
36. Reyer R.W. The amphibian eye: development and regeneration. In: Crescitelli F. (Ed). Handbook of Sensory Physiology (1977), Springer-Verlag, New York 309-390
37. Sakaguchi D.S., Janick L.M., and Reh T.A. Basic fibroblast growth factor (FGF-2) induced transdifferentiation of retinal pigment epithelium: generation of neurons and glia. Dev. Dyn. 209 (1997) 387-398
38. Schaefer J.J., Oliver G., and Henry J.J. Conservation of gene expression during embryonic lens formation and cornea-lens transdifferentiation in Xenopus laevis. Dev. Dyn. 215 (1999) 308-318
39. Sologub A.A. Mechanisms of repression and derepression of artificial transformation of pigmented epithelium into retina in Xenopus laevis. Roux's Arch. Dev. Biol. 182 (1977) 277-291
40. Stone L.S. Neural retina degeneration followed by regeneration from surviving retinal pigment cells in grafted adult salamander eyes. Anat. Rec. 106 (1950) 89-109
41. Straznicky K., and Gaze R.M. The growth of the retina in Xenopus laevis: an autoradiographic study. J. Embryol. Exp. Morphol. 26 (1971) 67-79
42. Straznicky C., and Hiscock J. Post-metamorphic retinal growth in Xenopus. Anat. Embryol. (Berl.) 69 (1984) 103-109
43. Tropepe V., Coles B.L., Chlasson B.J., Horsford D.J., Ella A.J., Mclnnes R.R., and Van der Kooy D. Retinal stem cells in the adult mammalian eye. Science 287 (2000) 2032-2036
44. Tsonis P.A. Regenerative biology. The emerging field of tissue repair and restoration. Differentiation 70 (2002) 397-409
45. Wallace H. Vertebrate Limb Regeneration (1981), Wiley, New York
46. Werb Z., and Chin J.R. Extracellular matrix remodeling during morphogenesis. Ann. N. Y. Acad. Sci. 857 (1998) 110-118