Synaptic inputs to broad thorny ganglion cells in macaque retina.
RRID: SCR_001622
RRID: SCR_017350
RRID:SCR_003584
RRID:SCR_005986
connectomics
electron microscopy
interneuron
motion sensitivity
primate
vision
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 08 2021
01 08 2021
Historique:
revised:
22
03
2021
received:
19
08
2020
accepted:
05
04
2021
pubmed:
13
4
2021
medline:
10
2
2022
entrez:
12
4
2021
Statut:
ppublish
Résumé
In primates, broad thorny retinal ganglion cells are highly sensitive to small, moving stimuli. They have tortuous, fine dendrites with many short, spine-like branches that occupy three contiguous strata in the middle of the inner plexiform layer. The neural circuits that generate their responses to moving stimuli are not well-understood, and that was the goal of this study. A connectome from central macaque retina was generated by serial block-face scanning electron microscopy, a broad thorny cell was reconstructed, and its synaptic inputs were analyzed. It received fewer than 2% of its inputs from both ON and OFF types of bipolar cells; the vast majority of its inputs were from amacrine cells. The presynaptic amacrine cells were reconstructed, and seven types were identified based on their characteristic morphology. Two types of narrow-field cells, knotty bistratified Type 1 and wavy multistratified Type 2, were identified. Two types of medium-field amacrine cells, ON starburst and spiny, were also presynaptic to the broad thorny cell. Three types of wide-field amacrine cells, wiry Type 2, stellate wavy, and semilunar Type 2, also made synapses onto the broad thorny cell. Physiological experiments using a macaque retinal preparation in vitro confirmed that broad thorny cells received robust excitatory input from both the ON and the OFF pathways. Given the paucity of bipolar cell inputs, it is likely that amacrine cells provided much of the excitatory input, in addition to inhibitory input.
Identifiants
pubmed: 33843050
doi: 10.1002/cne.25156
pmc: PMC8193796
mid: NIHMS1692873
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
3098-3111Subventions
Organisme : NIH HHS
ID : EY028927
Pays : United States
Organisme : NEI NIH HHS
ID : F32 EY007031
Pays : United States
Organisme : NIH HHS
ID : P51 OD010425
Pays : United States
Organisme : NEI NIH HHS
ID : P30 EY014800
Pays : United States
Organisme : NIH HHS
ID : P30-EY014800
Pays : United States
Organisme : NIH HHS
ID : EY002576
Pays : United States
Organisme : NIH HHS
ID : EY007031
Pays : United States
Organisme : NINDS NIH HHS
ID : T32 NS099578
Pays : United States
Organisme : NIH HHS
ID : P30-EY001730
Pays : United States
Organisme : NEI NIH HHS
ID : P30 EY001730
Pays : United States
Organisme : NIH HHS
ID : NS099578
Pays : United States
Organisme : NIH HHS
ID : P51-OD010425/ORID
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY028927
Pays : United States
Organisme : NIH HHS
ID : EY007125
Pays : United States
Organisme : NEI NIH HHS
ID : F32 EY032318
Pays : United States
Organisme : NEI NIH HHS
ID : T32 EY007125
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY002576
Pays : United States
Organisme : NEI NIH HHS
ID : T32 EY007031
Pays : United States
Organisme : NIH HHS
ID : EY027859
Pays : United States
Organisme : NEI NIH HHS
ID : R01 EY027859
Pays : United States
Informations de copyright
© 2021 Wiley Periodicals LLC.
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