Nonapical Symmetric Divisions Underlie Horizontal Cell Layer Formation in the Developing Retina In Vivo

Neuron

Volumn 56, Issue 4, 2007, Pages 597-603

  Godinho, Leanne ^a   Williams, Philip R ^a,b   Claassen, Yvonne ^c   Provost, Elayne ^d   Leach, Steven D ^d   Kamermans, Maarten ^c   Wong, Rachel O L ^a,b  

^a WASHINGTON UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF WASHINGTON   (United States)

^c NETHERLANDS INSTITUTE FOR NEUROSCIENCE   (Netherlands)

^d DEPARTMENT OF PATHOLOGY   (United States)

Author keywords

DEVBIO; MOLNEURO; STEMCELL

Indexed keywords

PANCREAS TRANSCRIPTION FACTOR 1A; PROTEIN; PROTEIN PROX1; TRANSCRIPTION FACTOR; UNCLASSIFIED DRUG;

ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CELL DIVISION; CELL POPULATION; CELL STRUCTURE; CELL TYPE; EMBRYO; EMBRYO DEVELOPMENT; IMAGING; MITOSIS; NONHUMAN; PHOTORECEPTOR; PRIORITY JOURNAL; PROTEIN EXPRESSION; RETINA DEVELOPMENT; STEM CELL; ZEBRA FISH;

ANIMALS; BIOLOGICAL MARKERS; BODY PATTERNING; CELL DIFFERENTIATION; CELL DIVISION; CELL SHAPE; GREEN FLUORESCENT PROTEINS; HOMEODOMAIN PROTEINS; LUMINESCENT PROTEINS; MICROSCOPY, CONFOCAL; NEURAL PATHWAYS; ORGANOGENESIS; PHOTORECEPTORS, VERTEBRATE; RETINA; RETINAL HORIZONTAL CELLS; STEM CELLS; SYNAPSES; TIME FACTORS; TRANSCRIPTION FACTORS; TUMOR SUPPRESSOR PROTEINS; ZEBRAFISH;

EID: 36048930160     PISSN: 08966273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuron.2007.09.036     Document Type: Article

References (45)

1. Bernardos R.L., Barthel L.K., Meyers J.R., and Raymond P.A. Late-stage neuronal progenitors in the retina are radial Muller glia that function as retinal stem cells. J. Neurosci. 27 (2007) 7028-7040
2. Connaughton V.P., Graham D., and Nelson R. Identification and morphological classification of horizontal, bipolar, and amacrine cells within the zebrafish retina. J. Comp. Neurol. 477 (2004) 371-385
3. D'Arcangelo G., Miao G.G., Chen S.C., Soares H.D., Morgan J.I., and Curran T. A protein related to extracellular matrix proteins deleted in the mouse mutant reeler. Nature 374 (1995) 719-723
4. Das T., Payer B., Cayouette M., and Harris W.A. In vivo time-lapse imaging of cell divisions during neurogenesis in the developing zebrafish retina. Neuron 37 (2003) 597-609
5. Dermietzel R., Kremer M., Paputsoglu G., Stang A., Skerrett I.M., Gomes D., Srinivas M., Janssen-Bienhold U., Weiler R., Nicholson B.J., et al. Molecular and functional diversity of neural connexins in the retina. J. Neurosci. 20 (2000) 8331-8343
6. Dyer M.A., Livesey F.J., Cepko C.L., and Oliver G. Prox1 function controls progenitor cell proliferation and horizontal cell genesis in the mammalian retina. Nat. Genet. 34 (2003) 53-58
7. Easter Jr. S.S., and Nicola G.N. The development of vision in the zebrafish (Danio rerio). Dev. Biol. 180 (1996) 646-663
8. Fischer A.J., and Reh T.A. Identification of a proliferating marginal zone of retinal progenitors in postnatal chickens. Dev. Biol. 220 (2000) 197-210
9. Fujitani Y., Fujitani S., Luo H., Qiu F., Burlison J., Long Q., Kawaguchi Y., Edlund H., Macdonald R.J., Furukawa T., et al. Ptf1a determines horizontal and amacrine cell fates during mouse retinal development. Development 133 (2006) 4439-4450
10. Godinho L., Mumm J.S., Williams P.R., Schroeter E.H., Koerber A., Park S.W., Leach S.D., and Wong R.O. Targeting of amacrine cell neurites to appropriate synaptic laminae in the developing zebrafish retina. Development 132 (2005) 5069-5079
11. Gonzalez J.L., Russo C.J., Goldowitz D., Sweet H.O., Davisson M.T., and Walsh C.A. Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype. J. Neurosci. 17 (1997) 9204-9211
12. Haubensak W., Attardo A., Denk W., and Huttner W.B. Neurons arise in the basal neuroepithelium of the early mammalian telencephalon: a major site of neurogenesis. Proc. Natl. Acad. Sci. USA 101 (2004) 3196-3201
13. Hendzel M.J., Wei Y., Mancini M.A., Van Hooser A., Ranalli T., Brinkley B.R., Bazett-Jones D.P., and Allis C.D. Mitosis-specific phosphorylation of histone H3 initiates primarily within pericentromeric heterochromatin during G2 and spreads in an ordered fashion coincident with mitotic chromosome condensation. Chromosoma 106 (1997) 348-360
14. Hinds J.W., and Hinds P.L. Differentiation of photoreceptors and horizontal cells in the embryonic mouse retina: an electron microscopic, serial section analysis. J. Comp. Neurol. 187 (1979) 495-511
15. Howell B.W., Hawkes R., Soriano P., and Cooper J.A. Neuronal position in the developing brain is regulated by mouse disabled-1. Nature 389 (1997) 733-737
16. Hu M., and Easter S.S. Retinal neurogenesis: the formation of the initial central patch of postmitotic cells. Dev. Biol. 207 (1999) 309-321
17. Jensen A.M., Walker C., and Westerfield M. mosaic eyes: a zebrafish gene required in pigmented epithelium for apical localization of retinal cell division and lamination. Development 128 (2001) 95-105
18. Johns P.R. Growth of the adult goldfish eye. III. Source of the new retinal cells. J. Comp. Neurol. 176 (1977) 343-357
19. Johns P.R. Formation of photoreceptors in larval and adult goldfish. J. Neurosci. 2 (1982) 178-198
20. Johns P.R., and Fernald R.D. Genesis of rods in teleost fish retina. Nature 293 (1981) 141-142
21. Julian D., Ennis K., and Korenbrot J.I. Birth and fate of proliferative cells in the inner nuclear layer of the mature fish retina. J. Comp. Neurol. 394 (1998) 271-282
22. Kirby B.B., Takada N., Latimer A.J., Shin J., Carney T.J., Kelsh R.N., and Appel B. In vivo time-lapse imaging shows dynamic oligodendrocyte progenitor behavior during zebrafish development. Nat. Neurosci. 9 (2006) 1506-1511
23. Koster R.W., and Fraser S.E. Tracing transgene expression in living zebrafish embryos. Dev. Biol. 233 (2001) 329-346
24. Kriegstein A., Noctor S., and Martinez-Cerdeno V. Patterns of neural stem and progenitor cell division may underlie evolutionary cortical expansion. Nat. Rev. Neurosci. 7 (2006) 883-890
25. Masai I., Yamaguchi M., Tonou-Fujimori N., Komori A., and Okamoto H. The hedgehog-PKA pathway regulates two distinct steps of the differentiation of retinal ganglion cells: the cell-cycle exit of retinoblasts and their neuronal maturation. Development 132 (2005) 1539-1553
26. Miyata T., Kawaguchi A., Saito K., Kawano M., Muto T., and Ogawa M. Asymmetric production of surface-dividing and non-surface-dividing cortical progenitor cells. Development 131 (2004) 3133-3145
27. Nakhai H., Sel S., Favor J., Mendoza-Torres L., Paulsen F., Duncker G.I., and Schmid R.M. Ptf1a is essential for the differentiation of GABAergic and glycinergic amacrine cells and horizontal cells in the mouse retina. Development 134 (2007) 1151-1160
28. Noctor S.C., Martinez-Cerdeno V., Ivic L., and Kriegstein A.R. Cortical neurons arise in symmetric and asymmetric division zones and migrate through specific phases. Nat. Neurosci. 7 (2004) 136-144
29. Otteson D.C., D'Costa A.R., and Hitchcock P.F. Putative stem cells and the lineage of rod photoreceptors in the mature retina of the goldfish. Dev. Biol. 232 (2001) 62-76
30. Poggi L., Vitorino M., Masai I., and Harris W.A. Influences on neural lineage and mode of division in the zebrafish retina in vivo. J. Cell Biol. 171 (2005) 991-999
31. Rapaport D.H., and Vietri A.J. Identity of cells produced by two stages of cytogenesis in the postnatal cat retina. J. Comp. Neurol. 312 (1991) 341-352
32. Rapaport D.H., Robinson S.R., and Stone J. Cytogenesis in the developing retina of the cat. Aust. N. Z. J. Ophthalmol. 13 (1985) 113-124
33. Raymond P.A., and Rivlin P.K. Germinal cells in the goldfish retina that produce rod photoreceptors. Dev. Biol. 122 (1987) 120-138
34. Robinson S.R., Rapaport D.H., and Stone J. Cell division in the developing cat retina occurs in two zones. Brain Res. 351 (1985) 101-109
35. Rompani S., and Cepko C. Retinal progenitor cells can produce restricted subsets of horizontal cells. Proc. Natl. Acad. Sci. USA (2007) in press
36. Sanes J.R., and Yamagata M. Formation of lamina-specific synaptic connections. Curr. Opin. Neurobiol. 9 (1999) 79-87
37. Schmitt E.A., and Dowling J.E. Early retinal development in the zebrafish, Danio rerio: light and electron microscopic analyses. J. Comp. Neurol. 404 (1999) 515-536
38. Schnitzer J., and Rusoff A.C. Horizontal cells of the mouse retina contain glutamic acid decarboxylase-like immunoreactivity during early developmental stages. J. Neurosci. 4 (1984) 2948-2955
39. Shields C.R., Klooster J., Claassen Y., Ul-Hussain M., Zoidl G., Dermietzel R., and Kamermans M. Retinal horizontal cell-specific promoter activity and protein expression of zebrafish connexin 52.6 and connexin 55.5. J. Comp. Neurol. 501 (2007) 765-779
40. Smirnov E.B., and Puchkov V.F. Characteristics of cellular proliferation in the developing human retina. Neurosci. Behav. Physiol. 34 (2004) 643-648
41. Turner D.L., Snyder E.Y., and Cepko C.L. Lineage-independent determination of cell type in the embryonic mouse retina. Neuron 4 (1990) 833-845
42. Wetts R., Serbedzija G.N., and Fraser S.E. Cell lineage analysis reveals multipotent precursors in the ciliary margin of the frog retina. Dev. Biol. 136 (1989) 254-263
43. Wong R.O., and Ghosh A. Activity-dependent regulation of dendritic growth and patterning. Nat. Rev. Neurosci. 3 (2002) 803-812
44. Yoneshima H., Nagata E., Matsumoto M., Yamada M., Nakajima K., Miyata T., Ogawa M., and Mikoshiba K. A novel neurological mutant mouse, yotari, which exhibits reeler-like phenotype but expresses CR-50 antigen/reelin. Neurosci. Res. 29 (1997) 217-223
45. Young R.W. Cell differentiation in the retina of the mouse. Anat. Rec. 212 (1985) 199-205