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Anat Embryol (Berl)
1986 Jan 01;1741:59-66. doi: 10.1007/bf00318336.
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Naturally occurring and induced ganglion cell death. A retinal whole-mount autoradiographic study in Xenopus.
Jenkins S
,
Straznicky C
.
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The retina in frogs grows continuously throughout the whole life of the animal by the addition of rings of cells at the ciliary margin. Naturally occurring neuron death cannot, consequently, be established by counting surviving neurons. A new approach, retinal whole-mount auto-radiography was introduced in this study to estimate cell loss occurring in the ganglion cell layer over a long period of time. 3H-thymidine injection at stage 53 (midlarval stage) labels a ring of cells, thereby marking the extent of retina formed up to the time of isotope administration. In the present study the number of neurons in the ganglion cell layer within the autoradiographically identified central retinal sector was estimated from midlarval stage to 6 months after metamorphosis in Xenopus laevis. The mean neuron number in the central retinal sector formed up to stage 53 was 17,420 and this was reduced by 20% to 13,515 by 6 months after metamorphosis. Optic nerve section at the time of isotope injection and subsequent regeneration brought about a reduction of the number of surviving neurons in the part of the retina formed up to stage 53 to 7,720, or to about 57% of the normal neuron number in an equivalent retinal area of an intact eye of the same age. A further reduction to 20% of normal neuron population was observed in retinae where the optic nerve failed to regenerate. The surviving neurons are assumed to be amacrine cells. The bulk of natural neuron loss in the retinal centre occurs during premetamorphic stages while little further loss takes place in the next 6 months suggesting that the underlying mechanism is a fine tuning of the developing retinal projections.
Beach,
Patterns of cell proliferation in the retina of the clawed frog during development.
1979, Pubmed,
Xenbase
Beach,
Patterns of cell proliferation in the retina of the clawed frog during development.
1979,
Pubmed
,
Xenbase
Bohn,
Retrograde degeneration of myelinated axons and re-organization in the optic nerves of adult frogs (Xenopus laevis) following nerve injury or tectal ablation.
1985,
Pubmed
,
Xenbase
Coleman,
Patterns of cell division during visual streak formation in the frog Limnodynastes dorsalis.
1984,
Pubmed
Dunlop,
Changing retinal ganglion cell distribution in the frog Heleioporus eyrei.
1981,
Pubmed
Dunlop,
A morphometric study of the retinal ganglion cell layer and optic nerve from metamorphosis in Xenopus laevis.
1984,
Pubmed
,
Xenbase
Fawcett,
Activity and the control of ganglion cell death in the rat retina.
1984,
Pubmed
Gaze,
The diencephalic course of regenerating retinotectal fibres in Xenopus tadpoles.
1978,
Pubmed
,
Xenbase
Gaze,
The evolution of the retinotectal map during development in Xenopus.
1974,
Pubmed
,
Xenbase
Glücksmann,
DEVELOPMENT AND DIFFERENTIATION OF THE TADPOLE EYE.
1940,
Pubmed
Grant,
Ontogeny of the retina and optic nerve in Xenopus laevis. I. Stages in the early development of the retina.
1980,
Pubmed
,
Xenbase
Hamburger,
Neuronal death in the spinal ganglia of the chick embryo and its reduction by nerve growth factor.
1981,
Pubmed
Hollyfield,
Differential addition of cells to the retina in Rana pipiens tadpoles.
1968,
Pubmed
Hollyfield,
Differential growth of the neural retina in Xenopus laevis larvae.
1971,
Pubmed
,
Xenbase
Hughes,
Ganglion cell death during normal retinal development in the chick: comparisons with cell death induced by early target field destruction.
1979,
Pubmed
Humphrey,
Retinal ganglion cell death during optic nerve regeneration in the frog Hyla moorei.
1985,
Pubmed
Jacobson,
Histogenesis of retina in the clawed frog with implications for the pattern of development of retinotectal connections.
1976,
Pubmed
,
Xenbase
Lam,
Loss of axons from the optic nerve of the rat during early postnatal development.
1982,
Pubmed
Potts,
The loss of ganglion cells in the developing retina of the rat.
1982,
Pubmed
Rager,
Generation and degeneration of retinal ganglion cells in the chicken.
1976,
Pubmed
Straznicky,
Retinal growth in double dorsal and double ventral eyes in Xenopus.
1977,
Pubmed
,
Xenbase
Straznicky,
The growth of the retina in Xenopus laevis: an autoradiographic study.
1971,
Pubmed
,
Xenbase
Straznicky,
Post-metamorphic retinal growth in Xenopus.
1984,
Pubmed
,
Xenbase
Straznicky,
The development of the retinotectal projections from compound eyes in Xenopus.
1981,
Pubmed
,
Xenbase
Straznicky,
Mapping retinal projections from double nasal and double temporal compound eyes to dually innervated tectum in Xenopus.
1981,
Pubmed
,
Xenbase
Straznicky,
Retinotectal map formation in dually innervated tecta: a regeneration study in Xenopus with one compound eye following bilateral optic nerve section.
1982,
Pubmed
,
Xenbase
Tay,
Temporo-nasal asymmetry in the accretion of retinal ganglion cells in late larval and postmetamorphic Xenopus.
1982,
Pubmed
,
Xenbase
Tay,
Aberrant retinotectal pathways induced by larval unilateral optic nerve section in Xenopus.
1980,
Pubmed
,
Xenbase
Wilson,
Optic nerve fibre counts and retinal ganglion cell counts during development of Xenopus laevis (Daudin).
1971,
Pubmed
,
Xenbase