期刊论文详细信息
Neural Development
Eye-specific retinogeniculate segregation proceeds normally following disruption of patterned spontaneous retinal activity
Hwai-Jong Cheng1  Barbara Chapman1  Ben K Stafford3  Lauren C Liets1  Chao Sun1  Colenso M Speer2 
[1] Department of Neurobiology, Physiology, and Behavior, University of California, Davis, One Shields Avenue, Davis, CA 95616, USA;Current address: Department of Chemistry and Chemical Biology, Harvard University, 12 Oxford Street, Cambridge, MA 02138, USA;Department of Neurosciences, University of California San Diego, 9500 Gilman Drive, San Diego, CA 92093, USA
关键词: Dorsal lateral geniculate nucleus;    Retinal ganglion cell;    Spontaneous activity;    Retinal wave;    Eye-specific segregation;    Retinogeniculate;   
Others  :  1146400
DOI  :  10.1186/1749-8104-9-25
 received in 2014-06-09, accepted in 2014-10-20,  发布年份 2014
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【 摘 要 】

Background

Spontaneous retinal activity (SRA) is important during eye-specific segregation within the dorsal lateral geniculate nucleus (dLGN), but the feature(s) of activity critical for retinogeniculate refinement are controversial. Pharmacologically or genetically manipulating cholinergic signaling during SRA perturbs correlated retinal ganglion cell (RGC) spiking and disrupts eye-specific retinofugal refinement in vivo, consistent with an instructive role for SRA during visual system development. Paradoxically, ablating the starburst amacrine cells (SACs) that generate cholinergic spontaneous activity disrupts correlated RGC firing without impacting retinal activity levels or eye-specific segregation in the dLGN. Such experiments suggest that patterned SRA during retinal waves is not critical for eye-specific refinement and instead, normal activity levels are permissive for retinogeniculate development. Here we revisit the effects of ablating the cholinergic network during eye-specific segregation and show that SAC ablation disrupts, but does not eliminate, retinal waves with no concomitant impact on normal eye-specific segregation in the dLGN.

Results

We induced SAC ablation in postnatal ferret pups beginning at birth by intraocular injection of a novel immunotoxin selective for the ferret vesicular acetylcholine transporter (Ferret VAChT-Sap). Through dual-patch whole-cell and multi-electrode array recording we found that SAC ablation altered SRA patterns and led to significantly smaller retinal waves compared with controls. Despite these defects, eye-specific segregation was normal. Further, interocular competition for target territory in the dLGN proceeded in cases where SAC ablation was asymmetric in the two eyes.

Conclusions

Our data demonstrate normal eye-specific retinogeniculate development despite significant abnormalities in patterned SRA. Comparing our current results with earlier studies suggests that defects in retinal wave size, absolute levels of SRA, correlations between RGC pairs, RGC burst frequency, high frequency RGC firing during bursts, and the number of spikes per RGC burst are each uncorrelated with abnormalities in eye-specific segregation in the dLGN. An increase in the fraction of asynchronous spikes occurring outside of bursts and waves correlates with eye-specific segregation defects in studies reported to date. These findings highlight the relative importance of different features of SRA while providing additional constraints for computational models of Hebbian plasticity mechanisms in the developing visual system.

【 授权许可】

   
2014 Speer et al.; licensee BioMed Central Ltd.

【 预 览 】
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