The growth of the retina in Xenopus laevis, an autoradiographic study

Development ◽  
1972 ◽  
Vol 27 (2) ◽  
pp. 381-387
Author(s):  
Joan D. Feldman ◽  
R. M. Gaze

The retina of Xenopus laevis has previously been shown, using autoradiographic methods, to develop in the normal animal by the annular addition of cells at the ciliary margin. The development of the retina in animals with surgically produced “compound eyes” was subsequently studied. In these animals the eye cup was split along the dorsoventral axis and the resulting half-eyes were recombined so as to form animals with a double-nasal eye. The retina in experimental animals was found to develop as in the normal animal. No labelling of cells with radioactive thymidine was seen along the cut edge of each half-eye; thus in terms of cell division each half of the compound eye remains a half.

Development ◽  
1971 ◽  
Vol 26 (1) ◽  
pp. 67-79
Author(s):  
K. Straznicky ◽  
R. M. Gaze

The growth of the retina has been studied in Xenopus by use of autoradiography with tritiated thymidine. At the time when retinal polarization first occurs (around stage 30) there are only some 20 ganglion cells across the retinal equator and the rest of the retina develops later, by annular addition of cells at the ciliary margin. This process continues beyond metamorphosis.


Development ◽  
1972 ◽  
Vol 28 (1) ◽  
pp. 87-115
Author(s):  
K. Straznicky ◽  
R. M. Gaze

The development of the optic tectum in Xenopus laevis has been studied by the use of autoradiography with tritiated thymidine. The first part of the adult tectum to form is the rostroventral pole; cells in this position undergo their final DNA synthesis between stages 35 and 45 or shortly thereafter. Next, the cells comprising the ventrolateral border of the tectum form. These cells undergo their final DNA synthesis at or shortly after stage 45. Finally the cells comprising the dorsal surface of the adult tectum form, mainly between stages 50–55. This part of the tectum originates from the serial addition of strips of cells medially, which displace the pre-existing tissue laterally and rostrally. The formation of the tectum is virtually complete by stage 58. The tectum in Xenopus thus forms in topographical order from rostroventral to caudo-medial. The distribution of labelled cells, several stages after the time of injection of isotope, indicates that, at any one time, a segment of tectum is forming which runs normal to the tectal surface and includes all layers from the ventricular layer out to the surface. In Xenopus, therefore, the times of origin of tectal cells appear to be related not to cell type or tectal layer but to the topographical position of the cells across the surface of the tectum.


Development ◽  
1981 ◽  
Vol 61 (1) ◽  
pp. 259-276
Author(s):  
Charles Straznicky ◽  
David Tay

Right compound eyes were formed in Xenopus embryos at stages 32–33 by the fusion of two nasal (NN), two ventral (VV) or two temporal (TT) halves. Shortly after metamorphosis the optic nerve from the compound eye was sectioned and the left intact eye removed. The retinotectal projections from the compound eye to the contralateral and ipsilateral tecta were studied by [3H]proline autoradiography and electrophysiological mapping between 6 weeks and 5 months after the postmetamorphic surgery. The results showed that NN and VV eyes projected to the entire extent of both tecta. In contrast, optic fibre projection from TT eyes, although more extensive than the normal temporal hemiretinal projection, failed to cover the caudomedial portion of the tecta. The visuotectal projections in all three combinations corresponded to typical reduplicated maps to be expected from such compound eyes, where each of the hemiretinae projected across the contralateral and ipsilateral tecta in an overlapping fashion. The rapid expansion of the hemiretinal projections of the compound eyes in the ipsilateral tectum following the removal of the resident optic fibre projection suggests that tectal markers may be carried and deployed by the incoming optic fibres themselves.


Development ◽  
1982 ◽  
Vol 72 (1) ◽  
pp. 225-249
Author(s):  
Charles Cima ◽  
Philip Grant

Development of the Xenopus laevis optic nerve was studied by light and electron microscopy from embryonic stage 26, before the retina has formed, to juveniles, 8 months post-metamorphic. Low-power EM photographs of sections through the retinal optic nerve (RON), middle optic nerve (MON) and chiasmatic optic nerve (CON) were prepared at different stages and the areas containing large axons (0·5 μm) were traced in optic nerve reconstructions. Ordering of fibre size along a dorsoventral axis was noted in the embryonic nerve, and this pattern persisted throughout development. Most large fibres, myelinated and unmyelinated, occupy an eccentric dorsocentral position in the MON while small axons are seen in a ventral peripheral crescent. In the CON, the dorsal one third to one half is occupied by large fibres while the ventral CON contains small fibres exclusively. If, as assumed, large axons are older than small axons (0·1–0·3 μm), then patterns of large and small axons along the nerve might reveal a chronotopic fibre ordering. Chronotopic ordering was confirmed by autoradiographic analysis of the distribution of old, labelled fibres and young, unlabelled newly arriving fibres in optic nerves between stage 51 and 57. The young—old labelling pattern corresponds to the small and large axon patterns respectively, in all sections of the optic nerve. Chronotopic ordering of fibres in the developing optic nerve can be explained, in part, by the dorsoventral asymmetric marginal growth of the developing retina and the phenomenon of fibre following as ganglion cell axons join near neighbour fascicles in the retina, converge at the optic disc and grow through the optic nerve.


2021 ◽  
Author(s):  
Montserrat Torres-Oliva ◽  
Elisa Buchberger ◽  
Alexandra D. Buffry ◽  
Maike Kittelmann ◽  
Lauren Sumner-Rooney ◽  
...  

The compound eyes of insects exhibit extensive variation in ommatidia number and size, which affects how they see and underlies adaptations in their vision to different environments and lifestyles. However, very little is known about the genetic and developmental bases underlying differences in compound eye size. We previously showed that the larger eyes of Drosophila mauritiana compared to D. simulans is caused by differences in ommatidia size rather than number. Furthermore, we identified an X-linked chromosomal region in D. mauritiana that results in larger eyes when introgressed into D. simulans. Here, we used a combination of fine-scale mapping and gene expression analysis to further investigate positional candidate genes on the X chromosome. We found that orthodenticle is expressed earlier in D. mauritiana than in D. simulans during ommatidial maturation in third instar larvae, and we further show that this gene is required for the correct organisation and size of ommatidia in D. melanogaster. Using ATAC-seq, we have identified several candidate eye enhancers of otd as well as potential direct targets of this transcription factor that are differentially expressed between D. mauritiana and D. simulans. Taken together, our results suggest that differential timing of otd expression contributes to natural variation in ommatidia size between D. mauritiana and D. simulans, which provides new insights into the mechanisms underlying the regulation and evolution of compound eye size in insects.


Development ◽  
1977 ◽  
Vol 40 (1) ◽  
pp. 175-185
Author(s):  
K. Straznicky ◽  
D. Tay

The growth of normal and surgically produced compound dorsal and ventral retinae in Xenopus laevis has been studied autoradiographically following injections of [3H]thymidine at stages 50 and 58. The animals were sacrificed 3 weeks after metamorphosis. The histogenetic pattern of the dorsal and ventral retinal halves was different at the three time points investigated, i.e. up to stage 50, between stages 50 and 58 and between stage 58 and 3 weeks after metamorphosis. Asymmetrical dorsal retinal growth occurred up to stage 50. From stage 50 onwards the retinal growth tendency reversed so that more ganglion cells were produced along the ventral than the dorsal ciliary margins. The overall preponderance of ventral retinal growth was 32·4% in cell number and 12·4% in retinal length from early embryogenesis to 3 weeks after metamorphosis. The characteristic histogenetic pattern of the dorsal and ventral retinal halves was maintained in an ectopic position in the compound eye, indicating that this particular property of the retinal halves is intrinsically determined.


Development ◽  
1975 ◽  
Vol 33 (3) ◽  
pp. 775-787
Author(s):  
Joan D. Feldman ◽  
R. M. Gaze

Double-nasal and double-temporal compound eyes were constructed in Xenopus embryos at stages 32 and 37/38. A particular half was removed from the host eye anlage and replaced with the opposite half-eye from the contralateral side of a donor embryo. Control operations consisted of removing a half-eye and replacing it with a similar half from the ipsilateral side of the donor embryo. Whereas in control animals, each half-eye projected its fibres to the appropriate half-tectum, in operated animals each half of the compound eye spread its optic teiminals across the entire rostrocaudal extent of the dorsal tectal surface. The area of tectal surface covered by ganglion fibre terminals was similar in operated animals mapped at successive stages of development to that previously observed in normal animals at equivalent stages. Therefore the factors responsible for the extended distribution of fibre terminals from each half of a compound eye must exist at least from mid-tadpole life, and thereafter be continuously present throughout development.


Development ◽  
1981 ◽  
Vol 66 (1) ◽  
pp. 159-174
Author(s):  
Charles Straznicky ◽  
David Tay

Right compound eyes were formed in Xenopus embryos at tailbud stages by the fusion of two nasal (NN), two temporal (TT) or two ventral (VV) halves. The left eye was kept intact. Two to four weeks after metamorphosis the optic nerve from the intact eye was severed to induce bilateral optic nerve regeneration. The contralateral retinotectal projections from the compound eye and the induced ipsilateral projections from the intact eye to the same (dually innervated) tectum were studied by [3H]proline autoradiography and visuotectal mapping from 3 to 6 months after the postmetamorphic surgery. The results showed that the NN, TT and VV projections, in the presence of optic fibres from the intact eye failed to spread across the whole extent of the dually innervated tectum. Unexpectedly the bulk of the regenerating projection from the intact eye was confined to the previously uninnervated parts of the dually innervated tecta, the caudomedial region in TT, the rostrolateral region in NN and the lateral region in VV eye animals. The partial segregation of the two populations of optic fibres in the dually innervated tectum has been taken as a further indication of the role of fibre-fibre and fibre-tectum interactions in retinotectal map formation.


1992 ◽  
Vol 171 (1) ◽  
pp. 373-393 ◽  
Author(s):  
THOMAS W. CRONIN ◽  
HONG Y. YAN ◽  
KAY D. BIDLE

1. Regional specialization within the triple compound eyes of the gonodactyloid stomatopod Gonodactylus oerstedii (Hansen) was studied by examining how ocular tracking of a small target was affected after occluding vision in particular ommatidial regions with black enamel paint. 2. Complete occlusion of one eye did not prevent the other eye from tracking, indicating that the two eyes act somewhat independently. However, following such treatment, the angular extent over which the seeing eye moved while tracking was reduced. 3. An eye was able to continue tracking a moving target even after occlusion of the anterior tip or after painting over all of its posterior surface except the anterior tip (restricting the visual field to a patch about 40° in diameter). Similarly, occlusion of only the midband, the medial half or the lateral half of an eye did not prevent tracking. 4. Tracking was also possible, although with decreased amplitude, when either the dorsal or the ventral hemisphere was occluded. However, when both the dorsal and ventral hemispheres were occluded, leaving only the midband for vision, the ability of an eye to track was abolished. 5. A computer model was used to investigate whether the midband alone had the potential to direct tracking in our experiments. The model's output predicts that, in spite of its restricted field of view, if the midband is oriented within 20° of the horizontal, an eye could track using the midband alone. Conditions favoring such potential tracking occurred in our experiments, but neither tracking nor targetting movements were observed. 6. We conclude that ommatidia of the dorsal and ventral hemispheres of each compound eye are essential for ocular tracking in G. oerstedii. The midband appears to play no major role in this activity. Note: Present address: Department of Zoology, The University of Maryland College Park, College Park, MD 20742, USA.


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