Deutsch
 
Hilfe Datenschutzhinweis Impressum
  DetailsucheBrowse

Datensatz

DATENSATZ AKTIONENEXPORT

Freigegeben

Zeitschriftenartikel

Connectomic analysis reveals an interneuron with an integral role in the retinal circuit for night vision

MPG-Autoren
/persons/resource/persons207101

Briggman,  Kevin L.
Department of Computational Neuroethology, Center of Advanced European Studies and Research (caesar), Max Planck Society;

Externe Ressourcen
Volltexte (beschränkter Zugriff)
Für Ihren IP-Bereich sind aktuell keine Volltexte freigegeben.
Volltexte (frei zugänglich)

elife-56077-v1.pdf
(Verlagsversion), 11MB

Ergänzendes Material (frei zugänglich)
Es sind keine frei zugänglichen Ergänzenden Materialien verfügbar
Zitation

Park, S. J. H., Lieberman, E. E., Ke, J.-B., Rho, N., Ghorbani, P., Rahmani, P., et al. (2020). Connectomic analysis reveals an interneuron with an integral role in the retinal circuit for night vision. eLife, 9: e56077. doi:10.7554/eLife.56077.


Zitierlink: https://hdl.handle.net/21.11116/0000-0006-7617-C
Zusammenfassung
Night vision in mammals depends fundamentally on rod photoreceptors and the well-studied rod bipolar (RB) cell pathway. The central neuron in this pathway, the AII amacrine cell (AC), exhibits a spatially tuned receptive field, composed of an excitatory center and an inhibitory surround, that propagates to ganglion cells, the retina’s projection neurons. The circuitry underlying the surround of the AII, however, remains unresolved. Here, we combined structural, functional and optogenetic analyses of the mouse retina to discover that surround inhibition of the AII depends primarily on a single interneuron type, the NOS-1 AC: a multistratified, axon-bearing GABAergic cell, with dendrites in both ON and OFF synaptic layers, but with a pure ON (depolarizing) response to light. Our study demonstrates generally that novel neural circuits can be identified from targeted connectomic analyses and specifically that the NOS-1 AC mediates long-range inhibition during night vision and is a major element of the RB pathway.