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Journal ArticleDOI

Patterns of cell proliferation in the retina of the clawed frog during development.

D. H. Beach, +1 more
- 01 Feb 1979 - 
- Vol. 183, Iss: 3, pp 603-613
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TLDR
In this paper, the spatial pattern of cell production in the developing retina of Xenopus has been made using 3H-thymidine labeling and colcemid blockade of mitosis, and the cell density remains constant throughout the retina, probably as a result of displacement of retinal cells dorsally to compensate for the relatively greater proliferation ventrally.
Abstract
Quantitative assays of the spatial pattern of cell production in the developing retina of Xenopus have been made using 3H-thymidine labelling and colcemid blockade of mitosis. Reconstructions were made from serial sections showing the position of every mitotic figure in the retina. After stage 54 the number of mitotic figures decreases at the dorsal margin of the retina and increases at the ventral margin. The ventral:dorsal ratio of mitoses reaches 10:1 by metamorphosis. Density of mitotic figures is maximum at the point of entry of the ophthalmic vessels at the ventral margin. In spite of asymmetrical production of retinal cells the cell density remains constant throughout the retina, probably as a result of displacement of retinal cells dorsally to compensate for the relatively greater proliferation ventrally. It is also proposed that the asymmetrical retinal growth serves to maintain the relationship between each point in visual space and corresponding points in the two retinae as the eyes are displaced dorsally on the head during metamorphosis.

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Citations
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Journal ArticleDOI

Retinal Stem Cells in the Adult Mammalian Eye

TL;DR: Adult retinal stem cells are localized to the pigmented ciliary margin and not to the central and peripheral retinal pigmented epithelium, indicating that these cells may be homologous to those found in the eye germinal zone of other nonmammalian vertebrates.
Journal ArticleDOI

Multipotent precursors can give rise to all major cell types of the frog retina.

TL;DR: Single optic vesicle cells have the potential to form any type of Retinal cell, suggesting that the interactions that specify the differentiation pathway of retinal cells must occur late in development.
Journal ArticleDOI

N-methyl-D-aspartate receptor antagonist desegregates eye-specific stripes.

TL;DR: Exposure of the optic tectum to NMDA results in stripes with sharper borders and fewer forks and fusions than untreated animals, suggesting that the NMDA receptor/channel plays a role in eye-specific segregation in the three-eyed tadpole.
Journal ArticleDOI

Proliferation, neurogenesis and regeneration in the non-mammalian vertebrate brain

TL;DR: The level of adult neurogenesis in vertebrates correlates with the capacity to regenerate injury, for example fish and amphibians exhibit the most widespread adult Neurogenesis and also the greatest capacity to regeneration central nervous system injuries.
Journal ArticleDOI

Adult neurogenesis and brain regeneration in zebrafish

TL;DR: The current knowledge on the stem cell niches, the characteristics of the stem/progenitor cells, how they are regulated and their involvement in the regeneration response of the adult zebrafish brain are discussed.
References
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Journal ArticleDOI

Growth of the adult goldfish eye. II. Increase in retinal cell number

TL;DR: An analysis of cell densities in various regions throughout the retina showed that the cells are distributed nearly homogeneously, which implies the formation of even more new synapses, and suggests the adult goldfish retina as a model for both neuro‐ and synaptogenesis.
Journal ArticleDOI

The Evolution of the Retinotectal Map during Development in Xenopus

TL;DR: The results of this study indicate a progressive shift of the retinotectal projection with development which may involve changing synaptic relations between retinal fibres and tectal cells.
Journal ArticleDOI

Cessation of DNA synthesis in retinal ganglion cells correlated with the time of specification of their central connections

TL;DR: Although no causal relationship has been shown, there appears to be a correlation between the cessation of DNA synthesis in ganglion cell neuroblasts at stages 28–29, and the specification of the central connections of theganglion cells at stages 29–31.
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