학술논문

Synaptic Specializations of Melanopsin-Retinal Ganglion Cells in Multiple Brain Regions Revealed by Genetic Label for Light and Electron Microscopy
Document Type
article
Source
Cell Reports. 29(3)
Subject
Biological Sciences
Eye Disease and Disorders of Vision
Neurosciences
1.1 Normal biological development and functioning
Underpinning research
Neurological
Animals
Axons
Brain
Circadian Rhythm
Female
Male
Mice
Mice
Knockout
Microscopy
Electron
Pretectal Region
Retinal Ganglion Cells
Rod Opsins
Suprachiasmatic Nucleus
Synapses
IGL
LGN
OPN
SCN
circadian
ipRGC
mRGC
melanopsin
miniSOG
serial blockface electron microscopy
Biochemistry and Cell Biology
Medical Physiology
Biological sciences
Language
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.