J. Ariga, S. L. Walker, and J. S. Mumm, Multicolor time-lapse imaging of transgenic zebrafish: visualizing retinal stem cells activated by targeted neuronal cell ablation, J. Vis. Exp. JoVE, 2010.

E. Arresta, S. Bernardini, E. Bernardini, S. Filoni, and S. M. Cannata, Pigmented epithelium to retinal transdifferentiation and Pax6 expression in larval Xenopus laevis, J. Exp. Zoolog. A Comp. Exp. Biol, vol.303, pp.958-967, 2005.

A. Arvidsson, T. Collin, D. Kirik, Z. Kokaia, and O. Lindvall, Neuronal replacement from endogenous precursors in the adult brain after stroke, Nat. Med, vol.8, pp.963-970, 2002.

B. Ayari, K. H. El-hachimi, C. Yanicostas, A. Landoulsi, and N. Soussi-yanicostas, Prokineticin 2 expression is associated with neural repair of injured adult zebrafish telencephalon, J. Neurotrauma, vol.27, pp.959-972, 2010.

B. Bally-cuif, L. Hammerschmidt, and M. , Induction and patterning of neuronal development, and its connection to cell cycle control, Curr. Opin. Neurobiol, vol.13, pp.16-25, 2003.

J. S. Barbosa, R. Sanchez-gonzalez, R. Di-giaimo, E. V. Baumgart, F. J. Theis et al., Neurodevelopment. Live imaging of adult neural stem cell behavior in the intact and injured zebrafish brain, vol.348, pp.789-793, 2015.

K. Barbosa-sabanero, A. Hoffmann, C. Judge, N. Lightcap, P. A. Tsonis et al., Lens and retina regeneration: new perspectives from model organisms, Biochem. J, vol.447, pp.321-334, 2012.

F. Barnabé-heider, C. Göritz, H. Sabelström, H. Takebayashi, F. W. Pfrieger et al., Origin of new glial cells in intact and injured adult spinal cord, Cell Stem Cell, vol.7, pp.470-482, 2010.

A. Barreiro-iglesias, K. S. Mysiak, A. L. Scott, M. M. Reimer, Y. Yang et al., Serotonin Promotes Development and Regeneration of Spinal Motor Neurons in Zebrafish, Cell Rep, vol.13, pp.924-932, 2015.

M. Bartkuhn, R. , and R. , Long range chromatin interactions involved in gene regulation, Biochim. Biophys. Acta, vol.1783, pp.2161-2166, 2008.

E. V. Baumgart, J. S. Barbosa, L. Bally-cuif, M. Götz, and J. Ninkovic, Stab wound injury of the zebrafish telencephalon: a model for comparative analysis of reactive gliosis, Glia, vol.60, pp.343-357, 2012.
URL : https://hal.archives-ouvertes.fr/hal-00683609

M. F. Beal, N. W. Kowall, D. W. Ellison, M. F. Mazurek, K. J. Swartz et al., Replication of the neurochemical characteristics of Huntington's disease by quinolinic acid, Nature, vol.321, pp.168-171, 1986.

T. Becker, M. F. Wullimann, C. G. Becker, R. R. Bernhardt, and M. Schachner, Axonal regrowth after spinal cord transection in adult zebrafish, J. Comp. Neurol, vol.377, pp.577-595, 1997.

A. L. Behrman, M. G. Bowden, and P. M. Nair, Neuroplasticity after spinal cord injury and training: an emerging paradigm shift in rehabilitation and walking recovery, Phys. Ther, vol.86, pp.1406-1425, 2006.

A. E. Bely and K. G. Nyberg, Evolution of animal regeneration: re-emergence of a field, Références bibliographiques, vol.25, p.139, 2010.

T. Ben-hur, O. Ben-menachem, V. Furer, O. Einstein, R. Mizrachi-kol et al., Effects of proinflammatory cytokines on the growth, fate, and motility of multipotential neural precursor cells, Mol. Cell. Neurosci, vol.24, pp.623-631, 2003.

D. A. Berg, M. Kirkham, A. Beljajeva, D. Knapp, B. Habermann et al., Efficient regeneration by activation of neurogenesis in homeostatically quiescent regions of the adult vertebrate brain, Dev. Camb. Engl, vol.137, pp.4127-4134, 2010.

S. Bernardini, C. Gargioli, S. M. Cannata, and S. Filoni, Neurogenesis during optic tectum regeneration in Xenopus laevis, Dev. Growth Differ, vol.52, pp.365-376, 2010.
DOI : 10.1111/j.1440-169x.2010.01176.x

R. L. Bernardos, R. , and P. A. , GFAP transgenic zebrafish, Gene Expr. Patterns GEP, vol.6, pp.1007-1013, 2006.
DOI : 10.1016/j.modgep.2006.04.006

R. L. Bernardos, L. K. Barthel, J. R. Meyers, R. , and P. A. , Late-Stage Neuronal Progenitors in the Retina Are Radial Müller Glia That Function as Retinal Stem Cells, J. Neurosci, vol.27, pp.7028-7040, 2007.

J. B. Bickenbach, C. Brown, and D. Burns, A global picture of spinal cord injury in international perspectives on spinal cord inury. World Health Organization, 2013.

E. J. Boniface, J. Lu, T. Victoroff, M. Zhu, C. et al., FlEx-based transgenic reporter lines for visualization of Cre and Flp activity in live zebrafish, Genes. N. Y. N, vol.47, pp.484-491, 2000.

J. E. Braisted, R. , and P. A. , Regeneration of dopaminergic neurons in goldfish retina, Dev. Camb. Engl, vol.114, pp.913-919, 1992.

J. E. Braisted, T. F. Essman, R. , and P. A. , Selective regeneration of photoreceptors in goldfish retina, Dev. Camb. Engl, vol.120, pp.2409-2419, 1994.

A. Bringmann, T. Pannicke, J. Grosche, M. Francke, P. Wiedemann et al., Müller cells in the healthy and diseased retina, Prog. Retin. Eye Res, vol.25, pp.397-424, 2006.

V. Broccoli, E. Boncinelli, and W. Wurst, The caudal limit of Otx2 expression positions the isthmic organizer, Nature, vol.401, pp.164-168, 1999.

J. P. Brockes and A. Kumar, Plasticity and reprogramming of differentiated cells in amphibian regeneration, Nat. Rev. Mol. Cell Biol, vol.3, pp.566-574, 2002.

A. Brombin, J. Grossier, A. Heuzé, Z. Radev, F. Bourrat et al., Genomewide analysis of the POU genes in medaka, focusing on expression in the optic tectum, Dev. Dyn. Off. Publ. Am. Assoc. Anat, vol.240, pp.2354-2363, 2011.
URL : https://hal.archives-ouvertes.fr/hal-00637198

C. Buckley, M. T. Carvalho, L. K. Young, S. A. Rider, C. Mcfadden et al., Precise spatio-temporal control of rapid optogenetic cell ablation with mem-KillerRed in, Zebrafish. Sci. Rep, vol.7, p.5096, 2017.

A. Buffo, I. Rite, P. Tripathi, A. Lepier, D. Colak et al., Origin and progeny of reactive gliosis: A source of multipotent cells in the injured brain, Proc. Natl. Acad. Sci. U. S. A, vol.105, pp.3581-3586, 2008.

M. E. Bulina, D. M. Chudakov, O. V. Britanova, Y. G. Yanushevich, D. B. Staroverov et al., A genetically encoded photosensitizer, Nat. Biotechnol, vol.24, pp.95-99, 2006.

J. E. Burda and M. V. Sofroniew, Reactive gliosis and the multicellular response to CNS damage and disease, Neuron, vol.81, pp.229-248, 2014.

C. A. Byrd and P. C. Brunjes, Addition of new cells to the olfactory bulb of adult zebrafish, Ann. N. Y. Acad. Sci, vol.855, pp.274-276, 1998.

E. Camand, M. Morel, A. Faissner, C. Sotelo, and I. Dusart, Long-term changes in the molecular composition of the glial scar and progressive increase of serotoninergic fibre sprouting after hemisection of the mouse spinal cord, Eur. J. Neurosci, vol.20, pp.1161-1176, 2004.
URL : https://hal.archives-ouvertes.fr/hal-00080982

D. A. Cameron, Cellular proliferation and neurogenesis in the injured retina of adult zebrafish, Vis. Neurosci, vol.17, pp.789-797, 2000.

D. A. Cameron and L. H. Carney, Cell mosaic patterns in the native and regenerated inner retina of zebrafish: implications for retinal assembly, J. Comp. Neurol, vol.416, pp.356-367, 2000.

D. A. Cameron and S. S. Easter, Cone photoreceptor regeneration in adult fish retina: phenotypic determination and mosaic pattern formation, J. Neurosci. Off. J. Soc. Neurosci, vol.15, pp.2255-2271, 1995.

M. Carlén, K. Meletis, C. Göritz, V. Darsalia, E. Evergren et al., Forebrain ependymal cells are Notch-dependent and generate neuroblasts and astrocytes after stroke, Nat. Neurosci, vol.12, pp.259-267, 2009.

F. Cavodeassi and C. Houart, Brain regionalization: of signaling centers and boundaries, Dev. Neurobiol, vol.72, pp.218-233, 2012.

L. Centanin, B. Hoeckendorf, and J. Wittbrodt, Fate restriction and multipotency in retinal stem cells, Cell Stem Cell, vol.9, pp.553-562, 2011.

L. Centanin, J. Ander, B. Hoeckendorf, K. Lust, T. Kellner et al., Exclusive multipotency and preferential asymmetric divisions in postembryonic neural stem cells of the fish retina, Dev. Camb. Engl, vol.141, pp.3472-3482, 2014.

K. L. Cerveny, M. Varga, W. , and S. W. , Continued growth and circuit building in the anamniote visual system, Dev. Neurobiol, vol.72, pp.328-345, 2012.

P. Chapouton, B. Adolf, C. Leucht, B. Tannhäuser, S. Ryu et al., her5 expression reveals a pool of neural stem cells in the adult zebrafish midbrain, Dev. Camb. Engl, vol.133, pp.4293-4303, 2006.

P. Chapouton, R. Jagasia, and L. Bally-cuif, Adult neurogenesis in non-mammalian vertebrates, BioEssays News Rev. Mol. Cell. Dev. Biol, vol.29, pp.745-757, 2007.

P. Chapouton, P. Skupien, B. Hesl, M. Coolen, J. C. Moore et al., Notch activity levels control the balance between quiescence and recruitment of adult neural stem cells, Références bibliographiques, vol.30, p.141, 2010.
URL : https://hal.archives-ouvertes.fr/hal-00506463

J. Chen, S. S. Magavi, and J. D. Macklis, Neurogenesis of corticospinal motor neurons extending spinal projections in adult mice, Proc. Natl. Acad. Sci. U. S. A, vol.101, pp.16357-16362, 2004.

S. Chera, L. Ghila, K. Dobretz, Y. Wenger, C. Bauer et al., Apoptotic cells provide an unexpected source of Wnt3 signaling to drive hydra head regeneration, Dev. Cell, vol.17, pp.279-289, 2009.

B. J. Chiasson, V. Tropepe, C. M. Morshead, and D. Van-der-kooy, Adult mammalian forebrain ependymal and subependymal cells demonstrate proliferative potential, but only subependymal cells have neural stem cell characteristics, J. Neurosci. Off. J. Soc. Neurosci, vol.19, pp.4462-4471, 1999.

B. H. Choi, Radial glia of developing human fetal spinal cord: Golgi, immunohistochemical and electron microscopic study, Brain Res, vol.227, pp.249-267, 1981.

T. Choi, N. Ninov, D. Y. Stainier, and D. Shin, Extensive conversion of hepatic biliary epithelial cells to hepatocytes after near total loss of hepatocytes in zebrafish, Gastroenterology, vol.146, pp.776-788, 2014.

R. M. Colwill, C. , and R. , Imaging escape and avoidance behavior in zebrafish larvae, Rev. Neurosci, vol.22, pp.63-73, 2011.

C. Conner, K. M. Ackerman, M. Lahne, J. S. Hobgood, and D. R. Hyde, Repressing notch signaling and expressing TNF? are sufficient to mimic retinal regeneration by inducing Müller glial proliferation to generate committed progenitor cells, J. Neurosci. Off. J. Soc. Neurosci, vol.34, pp.14403-14419, 2014.

M. Coolen and L. Bally-cuif, Microrégulation aux frontières (cérébrales), Med. Sci, vol.24, pp.787-789, 2008.

C. P. Corbo, N. A. Othman, M. C. Gutkin, A. D. Alonso, and Z. L. Fulop, Use of different morphological techniques to analyze the cellular composition of the adult zebrafish optic tectum, Microsc. Res. Tech, vol.75, pp.325-333, 2012.

S. G. Cummings and H. R. Bode, Head regeneration and polarity reversal inHydra attenuata can occur in the absence of DNA synthesis, Wilhelm Rouxs Arch. Dev. Biol, vol.194, pp.79-86, 1984.

S. Curado, R. M. Anderson, B. Jungblut, J. Mumm, E. Schroeter et al., Conditional targeted cell ablation in zebrafish: a new tool for regeneration studies, Dev. Dyn. Off. Publ. Am. Assoc. Anat, vol.236, pp.1025-1035, 2007.

E. Dambroise, M. Simion, T. Bourquard, S. Bouffard, B. Rizzi et al., Post-embryonic Fish Brain Proliferation Zones Exhibit Neuroepithelial-type Gene Expression Profile: Features of neuroepithelial cells in fish, STEM CELLS, 2017.

L. G. Darlington, G. M. Mackay, C. M. Forrest, N. Stoy, C. George et al., Altered kynurenine metabolism correlates with infarct volume in stroke, Eur. J. Neurosci, vol.26, pp.2211-2221, 2007.

J. M. Davison, C. M. Akitake, M. G. Goll, J. M. Rhee, N. Gosse et al., Transactivation from Gal4-VP16 transgenic insertions for tissue-specific cell labeling and ablation in zebrafish, Dev. Biol, vol.304, pp.811-824, 2007.

A. G. Dayer, A. A. Ford, K. M. Cleaver, M. Yassaee, C. et al., Short-term and longterm survival of new neurons in the rat dentate gyrus, J. Comp. Neurol, vol.460, pp.563-572, 2003.

F. Del-bene, A. M. Wehman, B. A. Link, and H. Baier, Regulation of neurogenesis by interkinetic nuclear migration through an apical-basal notch gradient, Cell, vol.134, pp.1055-1065, 2008.

F. Del-bene, C. Wyart, E. Robles, A. Tran, L. Looger et al., Filtering of visual information in the tectum by an identified neural circuit, Science, vol.330, pp.669-673, 2010.

C. B. Del-debbio, S. Balasubramanian, S. Parameswaran, A. Chaudhuri, F. Qiu et al., Notch and Wnt signaling mediated rod photoreceptor regeneration by Müller cells in adult mammalian retina, PloS One, vol.5, 2010.

R. J. Dempsey, K. A. Sailor, K. K. Bowen, K. Türeyen, and R. Vemuganti, Stroke-induced progenitor cell proliferation in adult spontaneously hypertensive rat brain: effect of exogenous IGF-1 and GDNF, J. Neurochem, vol.87, pp.586-597, 2003.

M. Devès and F. Bourrat, Transcriptional mechanisms of developmental cell cycle arrest: problems and models, Semin. Cell Dev. Biol, vol.23, pp.290-297, 2012.

V. Dewulf and S. W. Bottjer, Neurogenesis within the juvenile zebra finch telencephalic ventricular zone: a map of proliferative activity, J. Comp. Neurol, vol.481, pp.70-83, 2005.

T. B. Dias, Y. Yang, K. Ogai, T. Becker, and C. G. Becker, Notch signaling controls generation of motor neurons in the lesioned spinal cord of adult zebrafish, J. Neurosci. Off. J. Soc. Neurosci, vol.32, pp.3245-3252, 2012.

L. Dirian, S. Galant, M. Coolen, W. Chen, S. Bedu et al., , 2014.

, Spatial regionalization and heterochrony in the formation of adult pallial neural stem cells, Dev. Cell, vol.30, pp.123-136

F. Doetsch, I. Caillé, D. A. Lim, J. M. García-verdugo, and A. Alvarez-buylla, Subventricular zone astrocytes are neural stem cells in the adult mammalian brain, Cell, vol.97, pp.703-716, 1999.

W. Dong, R. H. Lee, H. Xu, S. Yang, K. G. Pratt et al., Visual avoidance in Xenopus tadpoles is correlated with the maturation of visual responses in the optic tectum, J. Neurophysiol, vol.101, pp.803-815, 2009.

D. Orazi, F. D. Zhao, X. Wong, R. O. , Y. et al., Mismatch of Synaptic Patterns between Neurons Produced in Regeneration and during Development of the Vertebrate Retina, Curr. Biol. CB, vol.26, pp.2268-2279, 2016.

D. I. Edwards, Nitroimidazole drugs-action and resistance mechanisms. I. Mechanisms of action, J. Antimicrob. Chemother, vol.31, pp.9-20, 1993.

M. A. Edwards, V. S. Caviness, and G. E. Schneider, Development of cell and fiber lamination in the mouse superior colliculus, J. Comp. Neurol, vol.248, pp.395-409, 1986.

C. Eifert, M. Farnworth, and T. Schutz-mirbach, Brain size variation in extremophile fish: local adaptation versus phenotypic plasticity, J. Zool, vol.295, issue.2, pp.143-153, 2014.

C. T. Ekdahl, J. Claasen, S. Bonde, Z. Kokaia, and O. Lindvall, Inflammation is detrimental for neurogenesis in adult brain, Proc. Natl. Acad. Sci. U. S. A, vol.100, pp.13632-13637, 2003.

P. Ekström, C. M. Johnsson, and L. M. Ohlin, Ventricular proliferation zones in the brain of an adult teleost fish and their relation to neuromeres and migration (secondary matrix) zones, J. Comp. Neurol, vol.436, pp.92-110, 2001.

W. A. El-kheir, H. Gabr, M. R. Awad, O. Ghannam, Y. Barakat et al., Autologous bone marrow-derived cell therapy combined with physical therapy induces functional improvement in chronic spinal cord injury patients, Cell Transplant, vol.23, pp.729-745, 2014.
DOI : 10.3727/096368913x664540
URL : http://journals.sagepub.com/doi/pdf/10.3727/096368913X664540

P. S. Eriksson, E. Perfilieva, T. Björk-eriksson, A. M. Alborn, C. Nordborg et al., Neurogenesis in the adult human hippocampus, Nat. Med, vol.4, pp.1313-1317, 1998.

M. P. Faillace, D. Julian, and J. I. Korenbrot, Mitotic activation of proliferative cells in the inner nuclear layer of the mature fish retina: regulatory signals and molecular markers, J. Comp. Neurol, vol.451, pp.127-141, 2002.

B. V. Fausett and D. Goldman, A role for alpha1 tubulin-expressing Müller glia in regeneration of the injured zebrafish retina, J. Neurosci. Off. J. Soc. Neurosci, vol.26, pp.6303-6313, 2006.

M. G. Fehlings and D. C. Baptiste, Current status of clinical trials for acute spinal cord injury, Injury, vol.36, issue.2, pp.113-122, 2005.
DOI : 10.1016/j.injury.2005.06.022

V. L. Feigin, M. H. Forouzanfar, R. Krishnamurthi, G. A. Mensah, M. Connor et al., Global and regional burden of stroke during 1990-2010: findings from the Global Burden of Disease Study, Lancet Lond. Engl, vol.383, pp.245-254, 2010.

R. J. Ferrante, N. W. Kowall, P. B. Cipolloni, E. Storey, and M. F. Beal, Excitotoxin lesions in primates as a model for Huntington's disease: histopathologic and neurochemical characterization, Exp. Neurol, vol.119, pp.46-71, 1993.
DOI : 10.1006/exnr.1993.1006

S. M. Fimbel, J. E. Montgomery, C. T. Burket, and D. R. Hyde, Regeneration of inner retinal neurons after intravitreal injection of ouabain in zebrafish, J. Neurosci. Off. J. Soc. Neurosci, vol.27, pp.1712-1724, 2007.

I. Foucher, M. Mione, A. Simeone, D. Acampora, L. Bally-cuif et al., Differentiation of cerebellar cell identities in absence of Fgf signalling in zebrafish Otx morphants, Dev. Camb. Engl, vol.133, pp.1891-1900, 2006.

B. Fraser, M. G. Duval, H. Wang, A. , and W. T. , Regeneration of cone photoreceptors when cell ablation is primarily restricted to a particular cone subtype, PloS One, vol.8, 2013.
DOI : 10.1371/journal.pone.0055410
URL : https://journals.plos.org/plosone/article/file?id=10.1371/journal.pone.0055410&type=printable

E. Gahtan, P. Tanger, and H. Baier, Visual prey capture in larval zebrafish is controlled by identified reticulospinal neurons downstream of the tectum, J. Neurosci. Off. J. Soc. Neurosci, vol.25, pp.9294-9303, 2005.

S. Galant, G. Furlan, M. Coolen, L. Dirian, I. Foucher et al., Embryonic origin and lineage hierarchies of the neural progenitor subtypes building the zebrafish adult midbrain, Dev. Biol, vol.420, pp.120-135, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01504429

J. Ganz, J. Kaslin, S. Hochmann, D. Freudenreich, and M. Brand, Heterogeneity and Fgf dependence of adult neural progenitors in the zebrafish telencephalon, Glia, vol.58, pp.1345-1363, 2010.

C. Gargioli and J. M. Slack, Cell lineage tracing during Xenopus tail regeneration, Dev. Camb. Engl, vol.131, pp.2669-2679, 2004.
DOI : 10.1242/dev.01155
URL : http://dev.biologists.org/content/131/11/2669.full.pdf

S. Ghosh and S. P. Hui, Regeneration of Zebrafish CNS: Adult Neurogenesis, Neural Plast, p.5815439, 2016.
DOI : 10.1155/2016/5815439
URL : http://downloads.hindawi.com/journals/np/2016/5815439.pdf

M. D. Ginsberg and R. Busto, Rodent models of cerebral ischemia, Stroke, vol.20, pp.1627-1642, 1989.
DOI : 10.1161/01.str.20.12.1627
URL : https://www.ahajournals.org/doi/pdf/10.1161/01.STR.20.12.1627

R. Godoy, S. Noble, K. Yoon, H. Anisman, and M. Ekker, Chemogenetic ablation of dopaminergic neurons leads to transient locomotor impairments in zebrafish larvae, J. Neurochem, vol.135, pp.249-260, 2015.

S. A. Goldman and F. Nottebohm, Neuronal production, migration, and differentiation in a vocal control nucleus of the adult female canary brain, Proc. Natl. Acad. Sci. U. S. A, vol.80, pp.2390-2394, 1983.

Y. Goldshmit, T. E. Sztal, P. R. Jusuf, T. E. Hall, M. Nguyen-chi et al., Fgf-dependent glial cell bridges facilitate spinal cord regeneration in zebrafish, J. Neurosci. Off. J. Soc. Neurosci, vol.32, pp.7477-7492, 2012.
DOI : 10.1523/jneurosci.0758-12.2012
URL : http://www.jneurosci.org/content/jneuro/32/22/7477.full.pdf

J. M. González-rosa, C. E. Burns, and C. G. Burns, Zebrafish heart regeneration: 15 years of discoveries, Regen. Oxf. Engl, vol.4, pp.105-123, 2017.

C. Göritz, D. O. Dias, N. Tomilin, M. Barbacid, O. Shupliakov et al., A pericyte origin of spinal cord scar tissue, Science, vol.333, pp.238-242, 2011.

M. Götz and W. B. Huttner, The cell biology of neurogenesis, Nat. Rev. Mol. Cell Biol, vol.6, pp.777-788, 2005.

M. Götz, S. Sirko, J. Beckers, and M. Irmler, Reactive astrocytes as neural stem or progenitor cells: In vivo lineage, In vitro potential, and Genome-wide expression analysis, Glia, vol.63, pp.1452-1468, 2015.

E. Gould, A. J. Reeves, M. Fallah, P. Tanapat, C. G. Gross et al., Hippocampal neurogenesis in adult Old World primates, Proc. Natl. Acad. Sci. U. S. A, vol.96, pp.5263-5267, 1999.
DOI : 10.1073/pnas.96.9.5263
URL : http://www.pnas.org/content/96/9/5263.full.pdf

E. Gramage, J. Li, and P. Hitchcock, The expression and function of midkine in the vertebrate retina, Br. J. Pharmacol, vol.171, pp.913-923, 2014.

H. Grandel and M. Brand, Comparative aspects of adult neural stem cell activity in vertebrates, Dev. Genes Evol, vol.223, pp.131-147, 2013.

H. Grandel, J. Kaslin, J. Ganz, I. Wenzel, and M. Brand, Neural stem cells and neurogenesis in the adult zebrafish brain: origin, proliferation dynamics, migration and cell fate, Dev. Biol, vol.295, pp.263-277, 2006.

E. A. Grove, Turning neurons into a nervous system, Références bibliographiques, vol.135, p.145, 2008.
DOI : 10.1242/dev.020511
URL : http://dev.biologists.org/content/135/13/2203.full.pdf

L. Grupp, H. Wolburg, M. , and A. F. , Astroglial structures in the zebrafish brain, J. Comp. Neurol, vol.518, pp.4277-4287, 2010.
DOI : 10.1002/cne.22511

G. J. Guillemin, Quinolinic acid, the inescapable neurotoxin, FEBS J, vol.279, pp.1356-1365, 2012.
DOI : 10.1111/j.1742-4658.2012.08485.x
URL : https://febs.onlinelibrary.wiley.com/doi/pdf/10.1111/j.1742-4658.2012.08485.x

C. P. Guise, J. I. Grove, E. I. Hyde, and P. F. Searle, Direct positive selection for improved nitroreductase variants using SOS triggering of bacteriophage lambda lytic cycle, Gene Ther, vol.14, pp.690-698, 2007.
DOI : 10.1038/sj.gt.3302919
URL : https://www.nature.com/articles/3302919.pdf

Y. Guo, L. Ma, M. Cristofanilli, R. P. Hart, A. Hao et al., Transcription factor Sox11b is involved in spinal cord regeneration in adult zebrafish, Neuroscience, vol.172, pp.329-341, 2011.
DOI : 10.1016/j.neuroscience.2010.10.026
URL : http://europepmc.org/articles/pmc3292217?pdf=render

G. F. Hagerman, N. C. Noel, S. Y. Cao, M. G. Duval, A. P. Oel et al., Rapid Recovery of Visual Function Associated with Blue Cone Ablation in Zebrafish, PloS One, vol.11, p.166932, 2016.

L. K. Hamilton, M. K. Truong, M. R. Bednarczyk, A. Aumont, and K. J. Fernandes, Cellular organization of the central canal ependymal zone, a niche of latent neural stem cells in the adult mammalian spinal cord, Neuroscience, vol.164, pp.1044-1056, 2009.

A. Hamon, J. E. Roger, X. Yang, and M. Perron, Müller glial cell-dependent regeneration of the neural retina: An overview across vertebrate model systems, Dev. Dyn. Off. Publ. Am. Assoc. Anat, vol.245, pp.727-738, 2016.

U. Hanisch and H. Kettenmann, Microglia: active sensor and versatile effector cells in the normal and pathologic brain, Nat. Neurosci, vol.10, pp.1387-1394, 2007.

M. J. Harding, H. F. Mcgraw, and A. Nechiporuk, The roles and regulation of multicellular rosette structures during morphogenesis, Dev. Camb. Engl, vol.141, pp.2549-2558, 2014.
DOI : 10.1242/dev.101444
URL : http://dev.biologists.org/content/141/13/2549.full.pdf

D. Hooker, Physiological reactions of goldfish with severed spinal cord, Proc. Soc. Exp. Biol. Med, vol.28, pp.89-90, 1930.
DOI : 10.3181/00379727-28-5170

L. L. Horky, F. Galimi, F. H. Gage, and P. J. Horner, Fate of endogenous stem/progenitor cells following spinal cord injury, J. Comp. Neurol, vol.498, pp.525-538, 2006.
DOI : 10.1002/cne.21065
URL : http://europepmc.org/articles/pmc2553041?pdf=render

C. Huber, J. Marschallinger, H. Tempfer, T. Furtner, S. Couillard-despres et al., Inhibition of leukotriene receptors boosts neural progenitor proliferation, Cell. Physiol. Biochem. Int. J. Exp. Cell. Physiol. Biochem. Pharmacol, vol.28, pp.793-804, 2011.

E. A. Huebner and S. M. Strittmatter, Axon regeneration in the peripheral and central nervous systems, Results Probl. Cell Differ, vol.48, pp.339-351, 2009.

A. A. Hyder, C. A. Wunderlich, P. Puvanachandra, G. Gururaj, and O. C. Kobusingye, The impact of traumatic brain injuries: a global perspective, NeuroRehabilitation, vol.22, pp.341-353, 2007.

I. Imayoshi, M. Sakamoto, T. Ohtsuka, and R. Kageyama, Continuous neurogenesis in the adult brain, Dev. Growth Differ, vol.51, pp.379-386, 2009.

J. Imitola, K. Raddassi, K. I. Park, F. Mueller, M. Nieto et al., Directed migration of neural stem cells to sites of CNS injury by the stromal cell-derived factor 1alpha/CXC chemokine receptor 4 pathway, Proc. Natl. Acad. Sci. U. S. A, vol.101, pp.18117-18122, 2004.

R. E. Iosif, C. T. Ekdahl, H. Ahlenius, C. J. Pronk, S. Bonde et al., Tumor necrosis factor receptor 1 is a negative regulator of progenitor proliferation in adult hippocampal neurogenesis, J. Neurosci. Off. J. Soc. Neurosci, vol.26, pp.9703-9712, 2006.

R. E. Iosif, H. Ahlenius, C. T. Ekdahl, V. Darsalia, P. Thored et al., Suppression of stroke-induced progenitor proliferation in adult subventricular zone by tumor necrosis factor receptor 1, J. Cereb. Blood Flow Metab. Off. J. Int. Soc. Cereb. Blood Flow Metab, vol.28, pp.1574-1587, 2008.

H. Ito, Y. Ishikawa, M. Yoshimoto, Y. , and N. , Diversity of brain morphology in teleosts: brain and ecological niche, Brain. Behav. Evol, vol.69, pp.76-86, 2007.

Y. Ito, H. Tanaka, H. Okamoto, and T. Ohshima, Characterization of neural stem cells and their progeny in the adult zebrafish optic tectum, Dev. Biol, vol.342, pp.26-38, 2010.

A. Jaerve and H. W. Müller, Chemokines in CNS injury and repair, Cell Tissue Res, vol.349, pp.229-248, 2012.

K. Jakubs, S. Bonde, R. E. Iosif, C. T. Ekdahl, Z. Kokaia et al., Inflammation regulates functional integration of neurons born in adult brain, J. Neurosci. Off. J. Soc. Neurosci, vol.28, pp.12477-12488, 2008.

K. Jin, M. Minami, J. Q. Lan, X. O. Mao, S. Batteur et al., , 2001.

, Neurogenesis in dentate subgranular zone and rostral subventricular zone after focal cerebral ischemia in the rat, Proc. Natl. Acad. Sci. U. S. A, vol.98, pp.4710-4715

K. Jin, Y. Zhu, Y. Sun, X. O. Mao, L. Xie et al., Vascular endothelial growth factor (VEGF) stimulates neurogenesis in vitro and in vivo, Proc. Natl. Acad. Sci. U. S. A, vol.99, pp.11946-11950, 2002.

K. Jin, Y. Sun, L. Xie, A. Peel, X. O. Mao et al., Directed migration of neuronal precursors into the ischemic cerebral cortex and striatum, Mol. Cell. Neurosci, vol.24, pp.171-189, 2003.

C. B. Johansson, S. Momma, D. L. Clarke, M. Risling, U. Lendahl et al., Identification of a neural stem cell in the adult mammalian central nervous system, Cell, vol.96, pp.25-34, 1999.

J. Joly, G. Recher, A. Brombin, K. Ngo, and V. Hartenstein, A Conserved Developmental Mechanism Builds Complex Visual Systems in Insects and Vertebrates, Curr. Biol. CB, vol.26, pp.1001-1009, 2016.
URL : https://hal.archives-ouvertes.fr/hal-01400057

N. L. Jorstad, M. S. Wilken, W. N. Grimes, S. G. Wohl, L. S. Vandenbosch et al., Stimulation of functional neuronal regeneration from Müller glia in adult mice, Références bibliographiques, vol.548, p.147, 2017.

J. Kang, J. Hu, R. Karra, A. L. Dickson, V. A. Tornini et al., Modulation of tissue repair by regeneration enhancer elements, Nature, vol.532, pp.201-206, 2016.

S. H. Kang, M. Fukaya, J. K. Yang, J. D. Rothstein, and D. E. Bergles, NG2+ CNS glial progenitors remain committed to the oligodendrocyte lineage in postnatal life and following neurodegeneration, Neuron, vol.68, pp.668-681, 2010.

J. Kaslin, J. Ganz, and M. Brand, Proliferation, neurogenesis and regeneration in the nonmammalian vertebrate brain, Philos. Trans. R. Soc. Lond. B. Biol. Sci, vol.363, pp.101-122, 2008.

J. Kaslin, J. Ganz, M. Geffarth, H. Grandel, S. Hans et al., Stem cells in the adult zebrafish cerebellum: initiation and maintenance of a novel stem cell niche, J. Neurosci. Off. J. Soc. Neurosci, vol.29, pp.6142-6153, 2009.

J. Kaslin, V. Kroehne, F. Benato, F. Argenton, and M. Brand, Development and specification of cerebellar stem and progenitor cells in zebrafish: from embryo to adult, 2013.

J. Kaslin, V. Kroehne, J. Ganz, S. Hans, and M. Brand, Distinct roles of neuroepithelial-like and radial glia-like progenitor cells in cerebellar regeneration, Dev. Camb. Engl, vol.144, pp.1462-1471, 2017.

N. J. Kee, E. Preston, and J. M. Wojtowicz, Enhanced neurogenesis after transient global ischemia in the dentate gyrus of the rat, Exp. Brain Res, vol.136, pp.313-320, 2001.

J. H. Keil, Functionnal spinal cord regeneration in adult rainbow-fish, Proc. Soc. Exp. Biol. Med, vol.43, pp.175-177, 1940.

C. B. Kimmel, W. W. Ballard, S. R. Kimmel, B. Ullmann, and T. F. Schilling, Stages of embryonic development of the zebrafish, Dev. Dyn. Off. Publ. Am. Assoc. Anat, vol.203, pp.253-310, 1995.

W. Kirsche, K. , and K. , , 1961.

, Z. Mikrosk. Anat. Forsch, vol.67, pp.140-182

N. Kishimoto, K. Shimizu, and K. Sawamoto, Neuronal regeneration in a zebrafish model of adult brain injury, Dis. Model. Mech, vol.5, pp.200-209, 2012.

C. Kizil, N. Kyritsis, S. Dudczig, V. Kroehne, D. Freudenreich et al., , 2012.

, Regenerative neurogenesis from neural progenitor cells requires injury-induced expression of Gata3, Dev. Cell, vol.23, pp.1230-1237

C. Kizil, S. Dudczig, N. Kyritsis, A. Machate, J. Blaesche et al., The chemokine receptor cxcr5 regulates the regenerative neurogenesis response in the adult zebrafish brain. Neural Develop. 7, p.27, 2012.

C. Kizil, J. Kaslin, V. Kroehne, and M. Brand, Adult neurogenesis and brain regeneration in zebrafish, Dev. Neurobiol, vol.72, pp.429-461, 2012.

C. Kizil, N. Kyritsis, and M. Brand, Effects of inflammation on stem cells: together they strive?, EMBO Rep, vol.16, pp.416-426, 2015.

J. R. Koke, A. L. Mosier, and D. M. García, Intermediate filaments of zebrafish retinal and optic nerve astrocytes and Müller glia: differential distribution of cytokeratin and GFAP, BMC Res. Notes, vol.3, p.50, 2010.

D. R. Kornack, R. , and P. , Continuation of neurogenesis in the hippocampus of the adult macaque monkey, Proc. Natl. Acad. Sci. U. S. A, vol.96, pp.5768-5773, 1999.

A. Kriegstein and A. Alvarez-buylla, The glial nature of embryonic and adult neural stem cells, Annu. Rev. Neurosci, vol.32, pp.149-184, 2009.

V. Kroehne, D. Freudenreich, S. Hans, J. Kaslin, and M. Brand, Regeneration of the adult zebrafish brain from neurogenic radial glia-type progenitors, Development, vol.138, pp.4831-4841, 2011.

G. Kurz-isler and H. Wolburg, Morphological study on the regeneration of the retina in the rainbow trout after ouabain-induced damage: evidence for dedifferentiation of photoreceptors, Cell Tissue Res, vol.225, pp.165-178, 1982.

V. Kuscha, S. L. Frazer, T. B. Dias, M. Hibi, T. Becker et al., Lesion-induced generation of interneuron cell types in specific dorsoventral domains in the spinal cord of adult zebrafish, J. Comp. Neurol, vol.520, pp.3604-3616, 2012.

N. Kyritsis, C. Kizil, S. Zocher, V. Kroehne, J. Kaslin et al., Acute inflammation initiates the regenerative response in the adult zebrafish brain, Science, vol.338, pp.1353-1356, 2012.

J. R. Lenkowski, R. , and P. A. , Müller glia: Stem cells for generation and regeneration of retinal neurons in teleost fish, Prog. Retin. Eye Res, vol.40, pp.94-123, 2014.

J. R. Lenkowski, Z. Qin, C. J. Sifuentes, R. Thummel, C. M. Soto et al., Retinal regeneration in adult zebrafish requires regulation of TGF? signaling, Glia, vol.61, pp.1687-1697, 2013.

R. B. Leonard, R. E. Coggeshall, W. , and W. D. , A documentation of an age related increase in neuronal and axonal numbers in the stingray, Dasyatis sabina, Leseuer. J. Comp. Neurol, vol.179, pp.13-21, 1978.

C. Leventhal, S. Rafii, D. Rafii, A. Shahar, and S. A. Goldman, Endothelial trophic support of neuronal production and recruitment from the adult mammalian subependyma, Mol. Cell. Neurosci, vol.13, pp.450-464, 1999.

L. Li, B. Yan, Y. Shi, W. Zhang, W. et al., Live imaging reveals differing roles of macrophages and neutrophils during zebrafish tail fin regeneration, J. Biol. Chem, vol.287, pp.25353-25360, 2012.

Y. Li, J. Chen, C. , and M. , Cell proliferation and differentiation from ependymal, subependymal and choroid plexus cells in response to stroke in rats, J. Neurol. Sci, vol.193, pp.137-146, 2002.

D. G. Lindmark and M. Müller, Antitrichomonad action, mutagenicity, and reduction of metronidazole and other nitroimidazoles, Antimicrob. Agents Chemother, vol.10, pp.476-482, 1976.

B. W. Lindsey, T. , and V. , A comparative framework for understanding the biological principles of adult neurogenesis, Prog. Neurobiol, vol.80, pp.281-307, 2006.

O. Lindvall, Z. Kokaia, and A. Martinez-serrano, Stem cell therapy for human neurodegenerative disorders-how to make it work, Nat. Med, vol.10, pp.42-50, 2004.

X. S. Liu, Z. G. Zhang, R. L. Zhang, S. Gregg, D. C. Morris et al., Stroke induces gene profile changes associated with neurogenesis and angiogenesis in adult subventricular zone progenitor cells, J. Cereb. Blood Flow Metab. Off. J. Int. Soc. Cereb. Blood Flow Metab, vol.27, pp.564-574, 2007.

Z. Liu, Y. Fan, S. J. Won, M. Neumann, D. Hu et al., Chronic treatment with minocycline preserves adult new neurons and reduces functional impairment after focal cerebral ischemia, Stroke, vol.38, pp.146-152, 2007.

C. Lois and A. Alvarez-buylla, Proliferating subventricular zone cells in the adult mammalian forebrain can differentiate into neurons and glia, Proc. Natl. Acad. Sci. U. S. A, vol.90, pp.2074-2077, 1993.

C. Lois, J. M. García-verdugo, and A. Alvarez-buylla, Chain migration of neuronal precursors, Science, vol.271, pp.978-981, 1996.

K. Lust, R. Sinn, A. Pérez-saturnino, L. Centanin, and J. Wittbrodt, De novo neurogenesis by targeted expression of atoh7 to Müller glia cells, Dev. Camb. Engl, vol.143, pp.1874-1883, 2016.

J. M. Lytle and J. R. Wrathall, Glial cell loss, proliferation and replacement in the contused murine spinal cord, Eur. J. Neurosci, vol.25, pp.1711-1724, 2007.

M. ,

M. M. Mader, C. , and D. A. , Photoreceptor differentiation during retinal development, growth, and regeneration in a metamorphic vertebrate, J. Neurosci. Off. J. Soc. Neurosci, vol.24, pp.11463-11472, 2004.

J. P. Magnusson, C. Göritz, J. Tatarishvili, D. O. Dias, E. M. Smith et al., A latent neurogenic program in astrocytes regulated by Notch signaling in the mouse, Science, vol.346, pp.237-241, 2014.

W. Maier and H. Wolburg, Regeneration of the goldfish retina after exposure to different doses of ouabain, Cell Tissue Res, vol.202, pp.99-118, 1979.

J. Mäkelä, R. Koivuniemi, L. Korhonen, and D. Lindholm, Interferon-gamma produced by microglia and the neuropeptide PACAP have opposite effects on the viability of neural progenitor cells, PloS One, vol.5, 2010.

P. Malatesta, E. Hartfuss, G. , and M. , Isolation of radial glial cells by fluorescent-activated cell sorting reveals a neuronal lineage, Dev. Camb. Engl, vol.127, pp.5253-5263, 2000.

P. Malatesta, M. A. Hack, E. Hartfuss, H. Kettenmann, W. Klinkert et al., Neuronal or glial progeny: regional differences in radial glia fate, Neuron, vol.37, pp.751-764, 2003.

P. Malatesta, I. Appolloni, C. , and F. , Radial glia and neural stem cells, Cell Tissue Res, vol.331, pp.165-178, 2008.

M. März, R. Schmidt, S. Rastegar, and U. Strähle, Expression of the transcription factor Olig2 in proliferating cells in the adult zebrafish telencephalon, Dev. Dyn. Off. Publ. Am. Assoc. Anat, vol.239, pp.3336-3349, 2010.

M. März, R. Schmidt, S. Rastegar, and U. Strähle, Regenerative response following stab injury in the adult zebrafish telencephalon, Dev. Dyn. Off. Publ. Am. Assoc. Anat, vol.240, pp.2221-2231, 2011.

J. Meek and N. A. Schellart, A Golgi study of goldfish optic tectum, J. Comp. Neurol, vol.182, pp.89-122, 1978.

K. Meletis, F. Barnabé-heider, M. Carlén, E. Evergren, N. Tomilin et al., Spinal cord injury reveals multilineage differentiation of ependymal cells, PLoS Biol, vol.6, p.182, 2008.

J. R. Meyers, L. Hu, A. Moses, K. Kaboli, A. Papandrea et al., ?-catenin/Wnt signaling controls progenitor fate in the developing and regenerating zebrafish retina. Neural Develop. 7, p.30, 2012.

G. K. Michalopoulos, Liver regeneration, J. Cell. Physiol, vol.213, pp.286-300, 2007.

A. Miyake, A. , and M. , Retinal stem/progenitor cells in the ciliary marginal zone complete retinal regeneration: a study of retinal regeneration in a novel animal model, Dev. Neurobiol, vol.74, pp.739-756, 2014.

M. H. Mokalled, C. Patra, A. L. Dickson, T. Endo, D. Y. Stainier et al., Injury-induced ctgfa directs glial bridging and spinal cord regeneration in zebrafish, Science, vol.354, pp.630-634, 2016.

J. R. Monaghan and M. Maden, Cellular plasticity during vertebrate appendage regeneration, Curr. Top. Microbiol. Immunol, vol.367, pp.53-74, 2013.

M. L. Monje, H. Toda, P. , and T. D. , Inflammatory blockade restores adult hippocampal neurogenesis, Science, vol.302, pp.1760-1765, 2003.

J. E. Montgomery, M. J. Parsons, and D. R. Hyde, A novel model of retinal ablation demonstrates that the extent of rod cell death regulates the origin of the regenerated zebrafish rod photoreceptors, J. Comp. Neurol, vol.518, pp.800-814, 2010.

T. Mori, A. Buffo, G. , and M. , The novel roles of glial cells revisited: the contribution of radial glia and astrocytes to neurogenesis, Curr. Top. Dev. Biol, vol.69, pp.67-99, 2005.

A. C. Morris, E. H. Schroeter, J. Bilotta, R. O. Wong, and J. M. Fadool, Cone survival despite rod degeneration in XOPS-mCFP transgenic zebrafish, Invest. Ophthalmol. Vis. Sci, vol.46, pp.4762-4771, 2005.

C. M. Morshead, B. A. Reynolds, C. G. Craig, M. W. Mcburney, W. A. Staines et al., Neural stem cells in the adult mammalian forebrain: a relatively quiescent subpopulation of subependymal cells, Neuron, vol.13, pp.1071-1082, 1994.

J. B. Moss, P. Koustubhan, M. Greenman, M. J. Parsons, I. Walter et al., Regeneration of the pancreas in adult zebrafish, Diabetes, vol.58, pp.1844-1851, 2009.

A. J. Mothe and C. H. Tator, Proliferation, migration, and differentiation of endogenous ependymal region stem/progenitor cells following minimal spinal cord injury in the adult rat, Neuroscience, vol.131, pp.177-187, 2005.

A. Muto, M. Ohkura, G. Abe, J. Nakai, and K. Kawakami, Real-time visualization of neuronal activity during perception, Références bibliographiques, vol.23, p.151, 2013.

H. Nakatomi, T. Kuriu, S. Okabe, S. Yamamoto, O. Hatano et al., Regeneration of hippocampal pyramidal neurons after ischemic brain injury by recruitment of endogenous neural progenitors, Cell, vol.110, pp.429-441, 2002.

G. Nato, A. Caramello, S. Trova, V. Avataneo, C. Rolando et al., Striatal astrocytes produce neuroblasts in an excitotoxic model of Huntington's disease, Dev. Camb. Engl, vol.142, pp.840-845, 2015.

K. Negishi, T. Teranishi, S. Kato, and Y. Nakamura, Paradoxical induction of dopaminergic cells following intravitreal injection of high doses of 6-hydroxydopamine in juvenile carp retina, Brain Res, vol.430, pp.67-79, 1987.

K. Negishi, K. Sugawara, S. Shinagawa, T. Teranishi, C. H. Kuo et al., Induction of immunoreactive proliferating cell nuclear antigen (PCNA) in goldfish retina following intravitreal injection with tunicamycin, Brain Res. Dev. Brain Res, vol.63, pp.71-83, 1991.

K. Negishi, W. K. Stell, T. Teranishi, A. Karkhanis, V. Owusu-yaw et al., Induction of proliferating cell nuclear antigen (PCNA)-immunoreactive cells in goldfish retina following intravitreal injection with 6-hydroxydopamine, Cell. Mol. Neurobiol, vol.11, pp.639-659, 1991.

C. M. Nelson, R. A. Gorsuch, T. J. Bailey, K. M. Ackerman, S. C. Kassen et al., Stat3 defines three populations of Müller glia and is required for initiating maximal müller glia proliferation in the regenerating zebrafish retina, J. Comp. Neurol, vol.520, pp.4294-4311, 2012.

C. M. Nelson, K. M. Ackerman, P. O'hayer, T. J. Bailey, R. A. Gorsuch et al., Tumor necrosis factor-alpha is produced by dying retinal neurons and is required for Muller glia proliferation during zebrafish retinal regeneration, J. Neurosci. Off. J. Soc. Neurosci, vol.33, pp.6524-6539, 2013.

L. M. Nevin, E. Robles, H. Baier, and E. K. Scott, Focusing on optic tectum circuitry through the lens of genetics, BMC Biol, vol.8, p.126, 2010.

V. Nguyen, K. Deschet, T. Henrich, E. Godet, J. S. Joly et al., Morphogenesis of the optic tectum in the medaka (Oryzias latipes): a morphological and molecular study, with special emphasis on cell proliferation, J. Comp. Neurol, vol.413, pp.385-404, 1999.
URL : https://hal.archives-ouvertes.fr/hal-00123336

R. Nieuwenhuys, The forebrain of actinopterygians revisited, Brain. Behav. Evol, vol.73, pp.229-252, 2009.

A. Nishiyama, M. Komitova, R. Suzuki, and X. Zhu, Polydendrocytes (NG2 cells): multifunctional cells with lineage plasticity, Nat. Rev. Neurosci, vol.10, pp.9-22, 2009.

S. C. Noctor, A. C. Flint, T. A. Weissman, W. S. Wong, B. K. Clinton et al., Dividing precursor cells of the embryonic cortical ventricular zone have morphological and molecular characteristics of radial glia, J. Neurosci. Off. J. Soc. Neurosci, vol.22, pp.3161-3173, 2002.

H. Nomura, H. Kim, A. Mothe, T. Zahir, I. Kulbatski et al., Endogenous radial glial cells support regenerating axons after spinal cord transection, Neuroreport, vol.21, pp.871-876, 2010.

K. Ogai, K. Nakatani, S. Hisano, K. Sugitani, Y. Koriyama et al., Function of Sox2 in ependymal cells of lesioned spinal cords in adult zebrafish, Neurosci. Res, vol.88, pp.84-87, 2014.

J. J. Ohab, S. Fleming, A. Blesch, and S. T. Carmichael, A neurovascular niche for neurogenesis after stroke, J. Neurosci. Off. J. Soc. Neurosci, vol.26, pp.13007-13016, 2006.

J. Ohnmacht, Y. Yang, G. W. Maurer, A. Barreiro-iglesias, T. M. Tsarouchas et al., Spinal motor neurons are regenerated after mechanical lesion and genetic ablation in larval zebrafish, Dev. Camb. Engl, vol.143, pp.1464-1474, 2016.

V. De-oliveira-carlos, J. Ganz, S. Hans, J. Kaslin, and M. Brand, Notch receptor expression in neurogenic regions of the adult zebrafish brain, PloS One, vol.8, 2013.

J. M. Parent, Z. S. Vexler, C. Gong, N. Derugin, and D. M. Ferriero, Rat forebrain neurogenesis and striatal neuron replacement after focal stroke, Ann. Neurol, vol.52, pp.802-813, 2002.

C. L. Parish, A. Beljajeva, E. Arenas, S. , and A. , Midbrain dopaminergic neurogenesis and behavioural recovery in a salamander lesion-induced regeneration model, Dev. Camb. Engl, vol.134, pp.2881-2887, 2007.

H. Park, J. Shin, R. K. Roberts, and B. Appel, An olig2 reporter gene marks oligodendrocyte precursors in the postembryonic spinal cord of zebrafish, Dev. Dyn. Off. Publ. Am. Assoc. Anat, vol.236, pp.3402-3407, 2007.

E. Pellegrini, K. Mouriec, I. Anglade, A. Menuet, Y. Le-page et al., Identification of aromatase-positive radial glial cells as progenitor cells in the ventricular layer of the forebrain in zebrafish, J. Comp. Neurol, vol.501, pp.150-167, 2007.
URL : https://hal.archives-ouvertes.fr/hal-00096389

V. Pencea, K. D. Bingaman, L. J. Freedman, and M. B. Luskin, Neurogenesis in the subventricular zone and rostral migratory stream of the neonatal and adult primate forebrain, Exp. Neurol, vol.172, pp.1-16, 2001.

L. A. Pennacchio, N. Ahituv, A. M. Moses, S. Prabhakar, M. A. Nobrega et al., In vivo enhancer analysis of human conserved noncoding sequences, Nature, vol.444, pp.499-502, 2006.

F. J. Perez-asensio, U. Perpiñá, A. M. Planas, P. , and E. , Interleukin-10 regulates progenitor differentiation and modulates neurogenesis in adult brain, J. Cell Sci, vol.126, pp.4208-4219, 2013.

L. Petreanu and A. Alvarez-buylla, Maturation and death of adult-born olfactory bulb granule neurons: role of olfaction, J. Neurosci. Off. J. Soc. Neurosci, vol.22, pp.6106-6113, 2002.

L. Pinto, G. , and M. , Radial glial cell heterogeneity-the source of diverse progeny in the CNS, Prog. Neurobiol, vol.83, pp.2-23, 2007.

H. Pisharath, J. M. Rhee, M. A. Swanson, S. D. Leach, and M. J. Parsons, Targeted ablation of beta cells in the embryonic zebrafish pancreas using E. coli nitroreductase, Références bibliographiques, vol.124, p.153, 2007.

J. Pollak, M. S. Wilken, Y. Ueki, K. E. Cox, J. M. Sullivan et al., , 2013.

, ASCL1 reprograms mouse Muller glia into neurogenic retinal progenitors, Dev. Camb. Engl, vol.140, pp.2619-2631

K. D. Poss, Advances in understanding tissue regenerative capacity and mechanisms in animals, Nat. Rev. Genet, vol.11, pp.710-722, 2010.

K. D. Poss, L. G. Wilson, and M. T. Keating, Heart regeneration in zebrafish, Science, vol.298, pp.2188-2190, 2002.

K. D. Poss, M. T. Keating, and A. Nechiporuk, Tales of regeneration in zebrafish, Dev. Dyn. Off. Publ. Am. Assoc. Anat, vol.226, pp.202-210, 2003.

V. E. Prince, R. M. Anderson, and G. Dalgin, Zebrafish Pancreas Development and Regeneration: Fishing for Diabetes Therapies, Curr. Top. Dev. Biol, vol.124, pp.235-276, 2017.

D. Purves, G. J. Augustine, D. Fitzptrick, J. M. Coquery, N. Tajeddine et al., , 2005.

Z. Qin, L. K. Barthel, R. , and P. A. , Genetic evidence for shared mechanisms of epimorphic regeneration in zebrafish, Proc. Natl. Acad. Sci. U. S. A, vol.106, pp.9310-9315, 2009.

R. Ramachandran, A. Reifler, J. M. Parent, and D. Goldman, Conditional gene expression and lineage tracing of tuba1a expressing cells during zebrafish development and retina regeneration, J. Comp. Neurol, vol.518, pp.4196-4212, 2010.

R. Ramachandran, B. V. Fausett, and D. Goldman, Ascl1a regulates Müller glia dedifferentiation and retinal regeneration through a Lin-28-dependent, let-7 microRNA signalling pathway, Nat. Cell Biol, vol.12, pp.1101-1107, 2010.

R. Ramachandran, X. Zhao, and D. Goldman, Ascl1a/Dkk/beta-catenin signaling pathway is necessary and glycogen synthase kinase-3beta inhibition is sufficient for zebrafish retina regeneration, Proc. Natl. Acad. Sci. U. S. A, vol.108, pp.15858-15863, 2011.

R. Ramachandran, X. Zhao, and D. Goldman, Insm1a-mediated gene repression is essential for the formation and differentiation of Müller glia-derived progenitors in the injured retina, Nat. Cell Biol, vol.14, pp.1013-1023, 2012.

M. Rapacioli, V. Palma, and V. Flores, Morphogenetic and Histogenetic Roles of the TemporalSpatial Organization of Cell Proliferation in the Vertebrate Corticogenesis as Revealed by Inter-specific Analyses of the Optic Tectum Cortex Development, Front. Cell. Neurosci, vol.10, p.67, 2016.

P. A. Raymond, Regeneration: New Neurons Wire Up, Curr. Biol. CB, vol.26, pp.794-796, 2016.
DOI : 10.1016/j.cub.2016.07.026

P. A. Raymond, M. J. Reifler, and P. K. Rivlin, Regeneration of goldfish retina: rod precursors are a likely source of regenerated cells, J. Neurobiol, vol.19, pp.431-463, 1988.

P. A. Raymond, L. K. Barthel, R. L. Bernardos, and J. J. Perkowski, Molecular characterization of retinal stem cells and their niches in adult zebrafish, BMC Dev. Biol, vol.6, p.36, 2006.

G. Recher, J. Jouralet, A. Brombin, A. Heuzé, E. Mugniery et al., Zebrafish midbrain slow-amplifying progenitors exhibit high levels of transcripts for nucleotide and ribosome biogenesis, Dev. Camb. Engl, vol.140, pp.4860-4869, 2013.
DOI : 10.1242/dev.099010
URL : https://hal.archives-ouvertes.fr/hal-00919928

M. M. Reimer, I. Sörensen, V. Kuscha, R. E. Frank, C. Liu et al., Motor neuron regeneration in adult zebrafish, J. Neurosci. Off. J. Soc. Neurosci, vol.28, pp.8510-8516, 2008.
DOI : 10.1523/jneurosci.1189-08.2008
URL : http://www.jneurosci.org/content/28/34/8510.full.pdf

M. M. Reimer, V. Kuscha, C. Wyatt, I. Sörensen, R. E. Frank et al., Sonic hedgehog is a polarized signal for motor neuron regeneration in adult zebrafish, J. Neurosci. Off. J. Soc. Neurosci, vol.29, pp.15073-15082, 2009.

M. M. Reimer, A. Norris, J. Ohnmacht, R. Patani, Z. Zhong et al., Dopamine from the brain promotes spinal motor neuron generation during development and adult regeneration, Dev. Cell, vol.25, pp.478-491, 2013.
DOI : 10.1016/j.devcel.2013.04.012
URL : https://doi.org/10.1016/j.devcel.2013.04.012

S. Robel, B. Berninger, G. , and M. , The stem cell potential of glia: lessons from reactive gliosis, Nat. Rev. Neurosci, vol.12, pp.88-104, 2011.

E. Robles, S. J. Smith, and H. Baier, Characterization of genetically targeted neuron types in the zebrafish optic tectum, Front. Neural Circuits, vol.5, 2011.

R. Rodriguez-viales, N. Diotel, M. Ferg, O. Armant, J. Eich et al., The helix-loop-helix protein id1 controls stem cell proliferation during regenerative neurogenesis in the adult zebrafish telencephalon, Stem Cells Dayt. Ohio, vol.33, pp.892-903, 2015.

T. Roeser and H. Baier, Visuomotor behaviors in larval zebrafish after GFP-guided laser ablation of the optic tectum, J. Neurosci. Off. J. Soc. Neurosci, vol.23, pp.3726-3734, 2003.

A. F. Rosenberg, M. A. Wolman, C. Franzini-armstrong, G. , and M. , In vivo nervemacrophage interactions following peripheral nerve injury, J. Neurosci. Off. J. Soc. Neurosci, vol.32, pp.3898-3909, 2012.

I. Rothenaigner, M. Krecsmarik, J. A. Hayes, B. Bahn, A. Lepier et al., Clonal analysis by distinct viral vectors identifies bona fide neural stem cells in the adult zebrafish telencephalon and characterizes their division properties and fate, Dev. Camb. Engl, vol.138, pp.1459-1469, 2011.
URL : https://hal.archives-ouvertes.fr/hal-00585364

H. Sabelström, M. Stenudd, P. Réu, D. O. Dias, M. Elfineh et al., Resident neural stem cells restrict tissue damage and neuronal loss after spinal cord injury in mice, Science, vol.342, pp.637-640, 2013.

H. Sabelström, M. Stenudd, and J. Frisén, Neural stem cells in the adult spinal cord, Exp. Neurol, vol.260, pp.44-49, 2014.

A. Sánchez-alvarado, Regeneration in the metazoans: why does it happen?, BioEssays News Rev. Mol. Cell. Dev. Biol, vol.22, pp.578-590, 2000.

F. C. Sauer, Mitosis in the neural tube, Références bibliographiques, vol.62, p.155, 1935.

E. K. Scott and H. Baier, The cellular architecture of the larval zebrafish tectum, as revealed by gal4 enhancer trap lines, Front. Neural Circuits, vol.3, p.13, 2009.

E. S. Seeley and M. V. Nachury, The perennial organelle: assembly and disassembly of the primary cilium, J. Cell Sci, vol.123, pp.511-518, 2010.

B. Seri, J. M. García-verdugo, B. S. Mcewen, and A. Alvarez-buylla, Astrocytes give rise to new neurons in the adult mammalian hippocampus, J. Neurosci. Off. J. Soc. Neurosci, vol.21, pp.7153-7160, 2001.

F. R. Sharp, J. Liu, and R. Bernabeu, Neurogenesis following brain ischemia, Brain Res. Dev. Brain Res, vol.134, pp.23-30, 2002.

I. S. Shimada, M. D. Lecomte, J. C. Granger, N. J. Quinlan, and J. L. Spees, Self-renewal and differentiation of reactive astrocyte-derived neural stem/progenitor cells isolated from the cortical peri-infarct area after stroke, J. Neurosci. Off. J. Soc. Neurosci, vol.32, pp.7926-7940, 2012.

C. Simon, M. Götz, and L. Dimou, Progenitors in the adult cerebral cortex: cell cycle properties and regulation by physiological stimuli and injury, Glia, vol.59, pp.869-881, 2011.

R. F. Sîrbulescu and G. K. Zupanc, Spinal cord repair in regeneration-competent vertebrates: adult teleost fish as a model system, Brain Res. Rev, vol.67, pp.73-93, 2011.

S. Sirko, G. Behrendt, P. A. Johansson, P. Tripathi, M. Costa et al., Reactive glia in the injured brain acquire stem cell properties in response to sonic hedgehog, 2013.

, Cell Stem Cell, vol.12, pp.426-439

K. Skaggs, D. Goldman, and J. M. Parent, Excitotoxic brain injury in adult zebrafish stimulates neurogenesis and long-distance neuronal integration, Glia, vol.62, pp.2061-2079, 2014.

N. Spassky, F. T. Merkle, N. Flames, A. D. Tramontin, J. M. García-verdugo et al., Adult ependymal cells are postmitotic and are derived from radial glial cells during embryogenesis, J. Neurosci. Off. J. Soc. Neurosci, vol.25, pp.10-18, 2005.

C. Stigloher, P. Chapouton, B. Adolf, and L. Bally-cuif, Identification of neural progenitor pools by E(Spl) factors in the embryonic and adult brain, Brain Res. Bull, vol.75, pp.266-273, 2008.
URL : https://hal.archives-ouvertes.fr/hal-01055285

T. W. Stone, C. M. Forrest, N. Stoy, and L. G. Darlington, Involvement of kynurenines in Huntington's disease and stroke-induced brain damage, J. Neural Transm, vol.119, pp.261-274, 1996.

M. L. Suster, H. Kikuta, A. Urasaki, K. Asakawa, and K. Kawakami, Transgenesis in zebrafish with the tol2 transposon system, Methods Mol. Biol. Clifton NJ, vol.561, pp.41-63, 2009.

K. Takahashi, K. Tanabe, M. Ohnuki, M. Narita, T. Ichisaka et al., Induction of pluripotent stem cells from adult human fibroblasts by defined factors, Cell, vol.131, pp.861-872, 2007.

K. Takasawa, K. Kitagawa, Y. Yagita, T. Sasaki, S. Tanaka et al., Increased proliferation of neural progenitor cells but reduced survival of newborn cells in the contralateral hippocampus after focal cerebral ischemia in rats, J. Cereb. Blood Flow Metab. Off. J. Int. Soc. Cereb. Blood Flow Metab, vol.22, pp.299-307, 2002.

A. Tallafuss and L. Bally-cuif, Tracing of her5 progeny in zebrafish transgenics reveals the dynamics of midbrain-hindbrain neurogenesis and maintenance, Dev. Camb. Engl, vol.130, pp.4307-4323, 2003.

E. Taverna and W. B. Huttner, Neural progenitor nuclei IN motion, Neuron, vol.67, pp.906-914, 2010.

C. Teh, D. M. Chudakov, K. Poon, I. Z. Mamedov, J. Sek et al., Optogenetic in vivo cell manipulation in KillerRed-expressing zebrafish transgenics, BMC Dev. Biol, vol.10, p.110, 2010.

S. Temple, The development of neural stem cells, Nature, vol.414, pp.112-117, 2001.

E. Than-trong and L. Bally-cuif, Radial glia and neural progenitors in the adult zebrafish central nervous system, Glia, vol.63, pp.1406-1428, 2015.
URL : https://hal.archives-ouvertes.fr/hal-01156471

J. L. Thomas, C. M. Nelson, X. Luo, D. R. Hyde, and R. Thummel, Characterization of multiple light damage paradigms reveals regional differences in photoreceptor loss, Exp. Eye Res, vol.97, pp.105-116, 2012.

J. L. Thomas, A. H. Ranski, G. W. Morgan, and R. Thummel, Reactive gliosis in the adult zebrafish retina, Exp. Eye Res, vol.143, pp.98-109, 2016.

P. Thored, J. Wood, A. Arvidsson, J. Cammenga, Z. Kokaia et al., Long-term neuroblast migration along blood vessels in an area with transient angiogenesis and increased vascularization after stroke, Stroke, vol.38, pp.3032-3039, 2007.

R. Thummel, S. C. Kassen, J. E. Montgomery, J. M. Enright, and D. R. Hyde, Inhibition of Müller glial cell division blocks regeneration of the light-damaged zebrafish retina, Dev. Neurobiol, vol.68, pp.392-408, 2008.

A. B. Tonchev, T. Yamashima, K. Sawamoto, and H. Okano, Enhanced proliferation of progenitor cells in the subventricular zone and limited neuronal production in the striatum and neocortex of adult macaque monkeys after global cerebral ischemia, J. Neurosci. Res, vol.81, pp.776-788, 2005.

J. W. Von-trotha, P. Vernier, and L. Bally-cuif, Emotions and motivated behavior converge on an amygdala-like structure in the zebrafish, Eur. J. Neurosci, vol.40, pp.3302-3315, 2014.
URL : https://hal.archives-ouvertes.fr/hal-01142430

H. Tuge and S. Hanzawa, Physiological and morphological regeneration on the sectioned spinal cord in adult teleosts, J. Comp. Neurol, vol.67, pp.343-365, 1937.

Y. Ueki, M. S. Wilken, K. E. Cox, L. Chipman, N. Jorstad et al., Transgenic expression of the proneural transcription factor Ascl1 in Müller glia stimulates retinal regeneration in young mice, Proc. Natl. Acad. Sci. U. S. A, vol.112, pp.13717-13722, 2015.

T. S. Vihtelic and D. R. Hyde, Light-induced rod and cone cell death and regeneration in the adult albino zebrafish (Danio rerio) retina, J. Neurobiol, vol.44, pp.289-307, 2000.

R. Villegas, S. M. Martin, K. C. O'donnell, S. A. Carrillo, A. Sagasti et al., Dynamics of degeneration and regeneration in developing zebrafish peripheral axons reveals a requirement for extrinsic cell types, p.157, 2012.

A. Visel, S. Minovitsky, I. Dubchak, and L. A. Pennacchio, VISTA Enhancer Browser-a database of tissue-specific human enhancers, Nucleic Acids Res, vol.35, pp.88-92, 2007.

J. Wan, R. Ramachandran, and D. Goldman, HB-EGF is necessary and sufficient for Müller glia dedifferentiation and retina regeneration, Dev. Cell, vol.22, pp.334-347, 2012.

Y. Wang, M. Rovira, S. Yusuff, and M. J. Parsons, Genetic inducible fate mapping in larval zebrafish reveals origins of adult insulin-producing ?-cells, Dev. Camb. Engl, vol.138, pp.609-617, 2011.

D. Wehner, T. M. Tsarouchas, A. Michael, C. Haase, G. Weidinger et al., Wnt signaling controls pro-regenerative Collagen XII in functional spinal cord regeneration in zebrafish, Nat. Commun, vol.8, p.126, 2017.

R. M. White, A. Sessa, C. Burke, T. Bowman, J. Leblanc et al., Transparent adult zebrafish as a tool for in vivo transplantation analysis, Cell Stem Cell, vol.2, pp.183-189, 2008.

Y. A. White, D. C. Woods, and A. W. Wood, A transgenic zebrafish model of targeted oocyte ablation and de novo oogenesis, Dev. Dyn. Off. Publ. Am. Assoc. Anat, vol.240, pp.1929-1937, 2011.

M. I. Willardsen and B. A. Link, Cell biological regulation of division fate in vertebrate neuroepithelial cells, Dev. Dyn. Off. Publ. Am. Assoc. Anat, vol.240, pp.1865-1879, 2011.

B. Winner, C. M. Cooper-kuhn, R. Aigner, J. Winkler, and H. G. Kuhn, Long-term survival and cell death of newly generated neurons in the adult rat olfactory bulb, Eur. J. Neurosci, vol.16, pp.1681-1689, 2002.

S. A. Wolf, B. Steiner, A. Wengner, M. Lipp, T. Kammertoens et al., Adaptive peripheral immune response increases proliferation of neural precursor cells in the adult hippocampus, FASEB J. Off. Publ. Fed. Am. Soc. Exp. Biol, vol.23, pp.3121-3128, 2009.

T. Xiao, T. Roeser, W. Staub, and H. Baier, A GFP-based genetic screen reveals mutations that disrupt the architecture of the zebrafish retinotectal projection, Dev. Camb. Engl, vol.132, pp.2955-2967, 2005.

Y. Xiao, A. Faucherre, L. Pola-morell, J. M. Heddleston, T. Liu et al., High-resolution live imaging reveals axon-glia interactions during peripheral nerve injury and repair in zebrafish, Dis. Model. Mech, vol.8, pp.553-564, 2015.

Y. Yagita, K. Kitagawa, T. Ohtsuki, T. Ki, T. Miyata et al., Neurogenesis by progenitor cells in the ischemic adult rat hippocampus, Stroke, vol.32, pp.1890-1896, 2001.

M. Yamaguchi and K. Mori, Critical period for sensory experience-dependent survival of newly generated granule cells in the adult mouse olfactory bulb, Proc. Natl. Acad. Sci. U. S. A, vol.102, pp.9697-9702, 2005.

T. Yamashita, M. Ninomiya, P. Hernández-acosta, J. M. García-verdugo, T. Sunabori et al., Subventricular zone-derived neuroblasts migrate and differentiate into mature neurons in the post-stroke adult striatum, J. Neurosci. Off. J. Soc. Neurosci, vol.26, pp.6627-6636, 2006.

S. Yeo, M. Kim, H. Kim, T. Huh, and A. B. Chitnis, Fluorescent protein expression driven by her4 regulatory elements reveals the spatiotemporal pattern of Notch signaling in the nervous system of zebrafish embryos, Dev. Biol, vol.301, pp.555-567, 2007.

P. Yurco, C. , and D. A. , Responses of Müller glia to retinal injury in adult zebrafish, Vision Res, vol.45, pp.991-1002, 2005.

E. E. Zattara, K. W. Turlington, and A. E. Bely, Long-term time-lapse live imaging reveals extensive cell migration during annelid regeneration, BMC Dev. Biol, vol.16, p.6, 2016.

R. L. Zhang, Z. G. Zhang, L. Zhang, C. , and M. , Proliferation and differentiation of progenitor cells in the cortex and the subventricular zone in the adult rat after focal cerebral ischemia, Neuroscience, vol.105, pp.33-41, 2001.

R. L. Zhang, M. Chopp, C. Roberts, X. Liu, M. Wei et al., Stroke increases neural stem cells and angiogenesis in the neurogenic niche of the adult mouse, PloS One, vol.9, p.113972, 2014.

D. Y. Zhu, S. H. Liu, H. S. Sun, and Y. M. Lu, Expression of inducible nitric oxide synthase after focal cerebral ischemia stimulates neurogenesis in the adult rodent dentate gyrus, J. Neurosci. Off. J. Soc. Neurosci, vol.23, pp.223-229, 2003.

B. Zikopoulos, M. Kentouri, and C. R. Dermon, Proliferation zones in the adult brain of a sequential hermaphrodite teleost species (Sparus aurata), Brain. Behav. Evol, vol.56, pp.310-322, 2000.

G. K. Zupanc, Towards brain repair: Insights from teleost fish, Semin. Cell Dev. Biol, vol.20, pp.683-690, 2009.

G. K. Zupanc and I. Horschke, Proliferation zones in the brain of adult gymnotiform fish: a quantitative mapping study, J. Comp. Neurol, vol.353, pp.213-233, 1995.

G. K. Zupanc and R. F. Sîrbulescu, Adult neurogenesis and neuronal regeneration in the central nervous system of teleost fish, Eur. J. Neurosci, vol.34, pp.917-929, 2011.

G. K. Zupanc, K. Hinsch, and F. H. Gage, Proliferation, migration, neuronal differentiation, and long-term survival of new cells in the adult zebrafish brain, J. Comp. Neurol, vol.488, pp.290-319, 2005.