The retinotectal projections in relation to layer B and F of the chick tectum

2000 ◽  
Vol 38 ◽  
pp. S71
Author(s):  
J Naito
Development ◽  
1971 ◽  
Vol 26 (3) ◽  
pp. 523-542
Author(s):  
K. Straznicky ◽  
R. M. Gaze ◽  
M. J. Keating

The nature of the retinotectal projection from a compound (NN or TT) eye in Xenopus raises certain problems concerning the mode of formation of connexions between the eye and the tectum. Each half of the compound eye appears to spread its connexions across the entire extent of the (apparently normal) contralateral tectum. This could indicate a certain plasticity in the way in which optic fibres can connect with the tectum. Alternatively, it is conceivable that each (similar) half of the compound eye is only able to innervate its corresponding half-tectum; in which case the uninnervated half-tectum could remain undeveloped and the innervated half-tectum could overgrow to resemble a normal tectum. This mechanism would preserve the idea of a rigidly fixed cell-to-cell specificity between retina and tectum. In an attempt to distinguish between these two mechanisms (spreading or overgrown half-tectum) we have given each of a series of Xenopus embryos at stage 32 one compound eye (NN or TT). Then, shortly after metamorphosis, we uncrossed the optic chiasma and 6 months later recorded the retinotectal projections from each eye to the tecta. Thus by connecting up the normal eye to the suspect tectum, and the compound eye to the normal tectum, we used the normal side in each case to provide an indication of the degree of abnormality with which the other side was connected. The results showed that a compound eye (NN or TT), connected to a normal tectum, gave a typical reduplicated map across the entire tectum, whereas the normal eye, when connected to the tectum which was previously innervated by the compound eye, gave an approximately normal projection across the whole of that tectum. These results lead us to conclude that, in the Xenopus visual system, no strict cell-to-cell type specificity exists; rather, what is preserved throughout these experimental manoeuvres is the polarity and extent of the projection.


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 ◽  
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.


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