Unknown

Dataset Information

0

Glutamatergic Monopolar Interneurons Provide a Novel Pathway of Excitation in the Mouse Retina.


ABSTRACT: Excitatory and inhibitory neurons in the CNS are distinguished by several features, including morphology, transmitter content, and synapse architecture [1]. Such distinctions are exemplified in the vertebrate retina. Retinal bipolar cells are polarized glutamatergic neurons receiving direct photoreceptor input, whereas amacrine cells are usually monopolar inhibitory interneurons with synapses almost exclusively in the inner retina [2]. Bipolar but not amacrine cell synapses have presynaptic ribbon-like structures at their transmitter release sites. We identified a monopolar interneuron in the mouse retina that resembles amacrine cells morphologically but is glutamatergic and, unexpectedly, makes ribbon synapses. These glutamatergic monopolar interneurons (GluMIs) do not receive direct photoreceptor input, and their light responses are strongly shaped by both ON and OFF pathway-derived inhibitory input. GluMIs contact and make almost as many synapses as type 2 OFF bipolar cells onto OFF-sustained A-type (AOFF-S) retinal ganglion cells (RGCs). However, GluMIs and type 2 OFF bipolar cells possess functionally distinct light-driven responses and may therefore mediate separate components of the excitatory synaptic input to AOFF-S RGCs. The identification of GluMIs thus unveils a novel cellular component of excitatory circuits in the vertebrate retina, underscoring the complexity in defining cell types even in this well-characterized region of the CNS.

SUBMITTER: Della Santina L 

PROVIDER: S-EPMC4980212 | BioStudies | 2016-01-01

REPOSITORIES: biostudies

Similar Datasets

2013-01-01 | S-EPMC3737599 | BioStudies
1000-01-01 | S-EPMC5725423 | BioStudies
2012-01-01 | S-EPMC3524110 | BioStudies
2010-01-01 | S-EPMC2943350 | BioStudies
2014-01-01 | S-EPMC4254642 | BioStudies
2009-01-01 | S-EPMC3296562 | BioStudies
2017-01-01 | S-EPMC5477664 | BioStudies
2015-01-01 | S-EPMC4529965 | BioStudies
2016-01-01 | S-EPMC4871735 | BioStudies
2009-01-01 | S-EPMC2766457 | BioStudies