Selective synaptic connections in the retinal pathway for night vision.

AII amacrine cell RRID: AB_2079751 RRID: AB_2307351 RRID: AB_2315776 RRID: AB_2536190 retina retinal ganglion cells rod bipolar cell scotopic vision synapse

Journal

The Journal of comparative neurology
ISSN: 1096-9861
Titre abrégé: J Comp Neurol
Pays: United States
ID NLM: 0406041

Informations de publication

Date de publication:
01 01 2019
Historique:
received: 02 06 2017
revised: 15 08 2017
accepted: 16 08 2017
pubmed: 1 9 2017
medline: 17 4 2020
entrez: 1 9 2017
Statut: ppublish

Résumé

The mammalian retina encodes visual information in dim light using rod photoreceptors and a specialized circuit: rods→rod bipolar cells→AII amacrine cell. The AII amacrine cell uses sign-conserving electrical synapses to modulate ON cone bipolar cell terminals and sign-inverting chemical (glycinergic) synapses to modulate OFF cone cell bipolar terminals; these ON and OFF cone bipolar terminals then drive the output neurons, retinal ganglion cells (RGCs), following light increments and decrements, respectively. The AII amacrine cell also makes direct glycinergic synapses with certain RGCs, but it is not well established how many types receive this direct AII input. Here, we investigated functional AII amacrine→RGC synaptic connections in the retina of the guinea pig (Cavia porcellus) by recording inhibitory currents from RGCs in the presence of ionotropic glutamate receptor (iGluR) antagonists. This condition isolates a specific pathway through the AII amacrine cell that does not require iGluRs: cone→ON cone bipolar cell→AII amacrine cell→RGC. These recordings show that AII amacrine cells make direct synapses with OFF Alpha, OFF Delta and a smaller OFF transient RGC type that co-stratifies with OFF Alpha cells. However, AII amacrine cells avoid making synapses with numerous RGC types that co-stratify with the connected RGCs. Selective AII connections ensure that a privileged minority of RGC types receives direct input from the night-vision pathway, independent from OFF bipolar cell activity. Furthermore, these results illustrate the specificity of retinal connections, which cannot be predicted solely by co-stratification of dendrites and axons within the inner plexiform layer.

Identifiants

pubmed: 28856684
doi: 10.1002/cne.24313
pmc: PMC5832573
mid: NIHMS919943
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

117-132

Subventions

Organisme : NEI NIH HHS
ID : P30 EY026878
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY014454
Pays : United States
Organisme : NEI NIH HHS
ID : P30 EY007003
Pays : United States
Organisme : NEI NIH HHS
ID : F31 EY007003
Pays : United States

Informations de copyright

© 2017 Wiley Periodicals, Inc.

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Auteurs

Deborah L Beaudoin (DL)

Department of Ophthalmology & Visual Sciences, University of Michigan, Ann Arbor, Michigan.

Mania Kupershtok (M)

Department of Ophthalmology & Visual Sciences, University of Michigan, Ann Arbor, Michigan.

Jonathan B Demb (JB)

Department of Ophthalmology & Visual Sciences, University of Michigan, Ann Arbor, Michigan.
Department of Molecular, Cellular & Developmental Biology, University of Michigan, Ann Arbor, Michigan.
Department of Ophthalmology & Visual Science, Yale University, New Haven, Connecticut.
Department of Cellular & Molecular Physiology, Yale University, New Haven, Connecticut.

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