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dc.contributor.authorHammer, Sarah
dc.contributor.authorCarrillo, Gabriela
dc.contributor.authorGovindaiah, Gubbi
dc.contributor.authorMonavarfeshani, Aboozar
dc.contributor.authorBircher, Joseph S.
dc.contributor.authorSu, Jianmin
dc.contributor.authorGuido, William
dc.contributor.authorFox, Michael A.
dc.date.accessioned2018-11-19T18:32:13Z
dc.date.available2018-11-19T18:32:13Z
dc.date.issued2014
dc.identifier.urihttp://hdl.handle.net/10919/85901
dc.description.abstractBackground: Mouse visual thalamus has emerged as a powerful model for understanding the mechanisms underlying neural circuit formation and function. Three distinct nuclei within mouse thalamus receive retinal input, the dorsal lateral geniculate nucleus (dLGN), the ventral lateral geniculate nucleus (vLGN), and the intergeniculate nucleus (IGL). However, in each of these nuclei, retinal inputs are vastly outnumbered by nonretinal inputs that arise from cortical and subcortical sources. Although retinal and nonretinal terminals associated within dLGN circuitry have been well characterized, we know little about nerve terminal organization, distribution and development in other nuclei of mouse visual thalamus. Results: Immunolabeling specific subsets of synapses with antibodies against vesicle-associated neurotransmitter transporters or neurotransmitter synthesizing enzymes revealed significant differences in the composition, distribution and morphology of nonretinal terminals in dLGN, vLGN and IGL. For example, inhibitory terminals are more densely packed in vLGN, and cortical terminals are more densely distributed in dLGN. Overall, synaptic terminal density appears least dense in IGL. Similar nuclei-specific differences were observed for retinal terminals using immunolabeling, genetic labeling, axonal tracing and serial block face scanning electron microscopy: retinal terminals are smaller, less morphologically complex, and more densely distributed in vLGN than in dLGN. Since glutamatergic terminal size often correlates with synaptic function, we used in vitro whole cell recordings and optic tract stimulation in acutely prepared thalamic slices to reveal that excitatory postsynaptic currents (EPSCs) are considerably smaller in vLGN and show distinct responses following paired stimuli. Finally, anterograde labeling of retinal terminals throughout early postnatal development revealed that anatomical differences in retinal nerve terminal structure are not observable as synapses initially formed, but rather developed as retinogeniculate circuits mature. Conclusions: Taken together, these results reveal nuclei-specific differences in nerve terminal composition, distribution, and morphology in mouse visual thalamus. These results raise intriguing questions about the different functions of these nuclei in processing light-derived information, as well as differences in the mechanisms that underlie their unique, nuclei-specific development.
dc.description.sponsorshipNational Institute of Health
dc.description.sponsorshipNIH: EY021222NIH: EY012716
dc.language.isoen_US
dc.publisherBMC
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectRetina
dc.subjectThalamus
dc.subjectRetinogeniculate
dc.subjectLateral geniculate nucleus
dc.subjectAxon
dc.subjectRetinal terminal
dc.subjectNerve terminal
dc.titleNuclei-specific differences in nerve terminal distribution, morphology, and development in mouse visual thalamus
dc.typeArticle - Refereed
dc.title.serialNeural Development
dc.identifier.doihttps://doi.org/10.1186/1749-8104-9-16
dc.identifier.volume9
dc.identifier.issue1
dc.type.dcmitypetext


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Attribution 4.0 International
License: Attribution 4.0 International