| Literature DB >> 31618632 |
Keun-Young Kim1, Luis C Rios2, Hiep Le2, Alex J Perez3, Sébastien Phan1, Eric A Bushong1, Thomas J Deerinck1, Yu Hsin Liu4, Maya A Ellisman5, Varda Lev-Ram6, Suyeon Ju3, Sneha A Panda3, Sanghee Yoon3, Masatoshi Hirayama2, Ludovic S Mure2, Megumi Hatori2, Mark H Ellisman7, Satchidananda Panda8.
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.Entities:
Keywords: IGL; LGN; OPN; SCN; circadian; ipRGC; mRGC; melanopsin; miniSOG; serial blockface electron microscopy
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Year: 2019 PMID: 31618632 PMCID: PMC7045601 DOI: 10.1016/j.celrep.2019.09.006
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423