AI Article Synopsis

  • The study investigates how retinal ganglion cells (RGCs) adapt when some cells die during the formation of a topographic map in the mouse brain.
  • Remaining RGCs expand their targeting area in the superior colliculus and increase spatial coverage in the retina, indicating a form of plasticity.
  • Despite these adjustments, the overall topographic map is maintained but is less precise, revealing the brain's ability to reorganize connections after retinal damage.

Article Abstract

The formation of the retinotopic map depends on the action of axon guidance molecules, activity-dependent mechanisms and axonal competition. However, little is known about the plasticity potential of the system and the effects on the remodelling of retinocollicular connections upon retinal insults. Here we create a mouse model in which retinal ganglion cells that project to anterior and posterior superior colliculus undergo cell death during topographic map formation. We show that the remaining retinal ganglion cells expand the targeted area in the superior colliculus and at the same time increase their spatial coverage in the retina in a correlated fashion. The resulting contralateral topographic map is overall maintained but less precise, while ipsilateral retinal ganglion cell axons are abnormally distributed in anterior and posterior superficial superior colliculus. These results suggest the presence of plastic mechanisms in the developing mammalian visual system to adjust retinal space and its target coverage and ensure a uniform map.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3709497PMC
http://dx.doi.org/10.1038/ncomms2926DOI Listing

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