Role of retinal input on the development of striate-extrastriate patterns of connections in the rat
Previous studies have shown that retinal input plays an important role in the development of interhemispheric callosal connections, but little is known about the role retinal input plays on the development of ipsilateral striate–extrastriate connections and the interplay that might exist between dev...
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Veröffentlicht in: | Journal of comparative neurology (1911) 2012-10, Vol.520 (14), p.3256-3276 |
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Sprache: | eng |
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Zusammenfassung: | Previous studies have shown that retinal input plays an important role in the development of interhemispheric callosal connections, but little is known about the role retinal input plays on the development of ipsilateral striate–extrastriate connections and the interplay that might exist between developing ipsilateral and callosal pathways. We analyzed the effects of bilateral enucleation performed at different ages on both the distribution of extrastriate projections originating from restricted loci in medial, acallosal striate cortex, and the overall pattern of callosal connections revealed following multiple tracer injections. As in normal rats, striate–extrastriate projections in rats enucleated at birth consisted of multiple, well‐defined fields that were largely confined to acallosal regions throughout extrastriate cortex. However, these projections were highly irregular and variable, and they tended to occupy correspondingly anomalous and variable acallosal regions. Moreover, area 17, but not area 18a, was smaller in enucleates compared to controls, resulting in an increase in the divergence of striate projections. Anomalies in patterns of striate–extrastriate projections were not observed in rats enucleated at postnatal day (P)6, although the size of area 17 was still reduced in these rats. These results indicate that the critical period during which the eyes influence the development of striate–extrastriate, but not the size of striate cortex, ends by P6. Finally, enucleation did not change the time course and definition of the initial invasion of axons into gray matter, suggesting that highly variable striate projections patterns do not result from anomalous pruning of exuberant distributions of 17–18a fibers in gray matter. J. Comp. Neurol., 520:3256–3276, 2012. © 2012 Wiley Periodicals, Inc. |
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ISSN: | 0021-9967 1096-9861 |
DOI: | 10.1002/cne.23096 |