| Literature DB >> 27426514 |
Luca Della Santina1, Sidney P Kuo2, Takeshi Yoshimatsu3, Haruhisa Okawa3, Sachihiro C Suzuki3, Mrinalini Hoon3, Kotaro Tsuboyama4, Fred Rieke2, Rachel O L Wong5.
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.Entities:
Mesh:
Substances:
Year: 2016 PMID: 27426514 PMCID: PMC4980212 DOI: 10.1016/j.cub.2016.06.016
Source DB: PubMed Journal: Curr Biol ISSN: 0960-9822 Impact factor: 10.834