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Cell Rep ; 29(3): 628-644.e6, 2019 10 15.
Article in English | MEDLINE | ID: mdl-31618632

ABSTRACT

The form and synaptic fine structure of melanopsin-expressing retinal ganglion cells, also called intrinsically photosensitive retinal ganglion cells (ipRGCs), were determined using a new membrane-targeted version of a genetic probe for correlated light and electron microscopy (CLEM). ipRGCs project to multiple brain regions, and because the method labels the entire neuron, it was possible to analyze nerve terminals in multiple retinorecipient brain regions, including the suprachiasmatic nucleus (SCN), olivary pretectal nucleus (OPN), and subregions of the lateral geniculate. Although ipRGCs provide the only direct retinal input to the OPN and SCN, ipRGC terminal arbors and boutons were found to be remarkably different in each target region. A network of dendro-dendritic chemical synapses (DDCSs) was also revealed in the SCN, with ipRGC axon terminals preferentially synapsing on the DDCS-linked cells. The methods developed to enable this analysis should propel other CLEM studies of long-distance brain circuits at high resolution.


Subject(s)
Brain/metabolism , Retinal Ganglion Cells/metabolism , Rod Opsins/metabolism , Synapses/metabolism , Animals , Axons/physiology , Brain/pathology , Circadian Rhythm/physiology , Female , Male , Mice , Mice, Knockout , Microscopy, Electron , Pretectal Region/metabolism , Pretectal Region/pathology , Retinal Ganglion Cells/pathology , Rod Opsins/deficiency , Rod Opsins/genetics , Suprachiasmatic Nucleus/metabolism , Suprachiasmatic Nucleus/pathology
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