A17 Amacrine Cells and Olfactory Granule Cells: Parallel Processors of Early Sensory Information

Neurons typically receive synaptic input in their dendritic arbor, integrate inputs in their soma, and send output action potentials through their axon, following Cajal’s law of dynamic polarization. Two notable exceptions are retinal amacrine cells and olfactory granule cells (GCs), which flout Caj...

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Main Authors: Veronica Egger, Jeffrey S. Diamond
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-11-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fncel.2020.600537/full
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spelling doaj-b2a62ac78c504e5e96a37e97647de71c2020-11-25T04:09:06ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022020-11-011410.3389/fncel.2020.600537600537A17 Amacrine Cells and Olfactory Granule Cells: Parallel Processors of Early Sensory InformationVeronica Egger0Jeffrey S. Diamond1Department of Neurophysiology, Institute of Zoology, Universität Regensburg, Regensburg, GermanySynaptic Physiology Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, United StatesNeurons typically receive synaptic input in their dendritic arbor, integrate inputs in their soma, and send output action potentials through their axon, following Cajal’s law of dynamic polarization. Two notable exceptions are retinal amacrine cells and olfactory granule cells (GCs), which flout Cajal’s edict by providing synaptic output from the same dendrites that collect synaptic input. Amacrine cells, a diverse cell class comprising >60 subtypes, employ various dendritic input/output strategies, but A17 amacrine cells (A17s) in particular share further interesting functional characteristics with GCs: both receive excitatory synaptic input from neurons in the primary glutamatergic pathway and return immediate, reciprocal feedback via GABAergic inhibitory synapses to the same synaptic terminals that provided input. Both neurons thereby process signals locally within their dendrites, shaping many parallels, signaling pathways independently. The similarities between A17s and GCs cast into relief striking differences that may indicate distinct processing roles within their respective circuits: First, they employ partially dissimilar molecular mechanisms to transform excitatory input into inhibitory output; second, GCs fire action potentials, whereas A17s do not. Third, GC signals may be influenced by cortical feedback, whereas the mammalian retina receives no such retrograde input. Finally, A17s constitute just one subtype within a diverse class that is specialized in a particular task, whereas the more homogeneous GCs may play more diverse signaling roles via multiple processing modes. Here, we review these analogies and distinctions between A17 amacrine cells and granule cells, hoping to gain further insight into the operating principles of these two sensory circuits.https://www.frontiersin.org/articles/10.3389/fncel.2020.600537/fullretinaolfactory bulbreciprocal synapseinhibitionparallel processinglocal feedback
collection DOAJ
language English
format Article
sources DOAJ
author Veronica Egger
Jeffrey S. Diamond
spellingShingle Veronica Egger
Jeffrey S. Diamond
A17 Amacrine Cells and Olfactory Granule Cells: Parallel Processors of Early Sensory Information
Frontiers in Cellular Neuroscience
retina
olfactory bulb
reciprocal synapse
inhibition
parallel processing
local feedback
author_facet Veronica Egger
Jeffrey S. Diamond
author_sort Veronica Egger
title A17 Amacrine Cells and Olfactory Granule Cells: Parallel Processors of Early Sensory Information
title_short A17 Amacrine Cells and Olfactory Granule Cells: Parallel Processors of Early Sensory Information
title_full A17 Amacrine Cells and Olfactory Granule Cells: Parallel Processors of Early Sensory Information
title_fullStr A17 Amacrine Cells and Olfactory Granule Cells: Parallel Processors of Early Sensory Information
title_full_unstemmed A17 Amacrine Cells and Olfactory Granule Cells: Parallel Processors of Early Sensory Information
title_sort a17 amacrine cells and olfactory granule cells: parallel processors of early sensory information
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2020-11-01
description Neurons typically receive synaptic input in their dendritic arbor, integrate inputs in their soma, and send output action potentials through their axon, following Cajal’s law of dynamic polarization. Two notable exceptions are retinal amacrine cells and olfactory granule cells (GCs), which flout Cajal’s edict by providing synaptic output from the same dendrites that collect synaptic input. Amacrine cells, a diverse cell class comprising >60 subtypes, employ various dendritic input/output strategies, but A17 amacrine cells (A17s) in particular share further interesting functional characteristics with GCs: both receive excitatory synaptic input from neurons in the primary glutamatergic pathway and return immediate, reciprocal feedback via GABAergic inhibitory synapses to the same synaptic terminals that provided input. Both neurons thereby process signals locally within their dendrites, shaping many parallels, signaling pathways independently. The similarities between A17s and GCs cast into relief striking differences that may indicate distinct processing roles within their respective circuits: First, they employ partially dissimilar molecular mechanisms to transform excitatory input into inhibitory output; second, GCs fire action potentials, whereas A17s do not. Third, GC signals may be influenced by cortical feedback, whereas the mammalian retina receives no such retrograde input. Finally, A17s constitute just one subtype within a diverse class that is specialized in a particular task, whereas the more homogeneous GCs may play more diverse signaling roles via multiple processing modes. Here, we review these analogies and distinctions between A17 amacrine cells and granule cells, hoping to gain further insight into the operating principles of these two sensory circuits.
topic retina
olfactory bulb
reciprocal synapse
inhibition
parallel processing
local feedback
url https://www.frontiersin.org/articles/10.3389/fncel.2020.600537/full
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