Cargando…

Voltage-dependent intrinsic bursting in olfactory bulb Golgi cells

In the mammalian olfactory bulb (OB), local synaptic circuits modulate the evolving pattern of activity in mitral and tufted cells following olfactory sensory stimulation. GABAergic granule cells, the most numerous interneuron subtype in this brain region, have been extensively studied. However, cla...

Descripción completa

Detalles Bibliográficos
Autores principales: Pressler, R. Todd, Rozman, Peter A., Strowbridge, Ben W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3744043/
https://www.ncbi.nlm.nih.gov/pubmed/23950193
http://dx.doi.org/10.1101/lm.031856.113
_version_ 1782280548706680832
author Pressler, R. Todd
Rozman, Peter A.
Strowbridge, Ben W.
author_facet Pressler, R. Todd
Rozman, Peter A.
Strowbridge, Ben W.
author_sort Pressler, R. Todd
collection PubMed
description In the mammalian olfactory bulb (OB), local synaptic circuits modulate the evolving pattern of activity in mitral and tufted cells following olfactory sensory stimulation. GABAergic granule cells, the most numerous interneuron subtype in this brain region, have been extensively studied. However, classic studies using Golgi staining methods identified many other, nongranule cell types in the OB whose function remains mysterious. Within just the granule cell layer (GCL), Ramón y Cajal described multiple morphologically distinct subtypes of nongranule interneurons including large spiny Blanes cells which exhibit intrinsic persistent activity. Here, we define the intrinsic electrophysiology of a different nongranule interneuronal cell type in the GCL described by Ramón y Cajal, sparsely spiny Golgi cells in the rat OB. Golgi cells exhibit two distinct firing modes depending on the membrane potential: tonic firing and bursting. Golgi cells also generate rebound bursts following the offset of hyperpolarizing steps. We find that both low-threshold burst responses to depolarizing inputs and rebound bursts are blocked by nickel, an antagonist of T-type voltage-gated Ca(2+) current. The state-dependent firing behavior we report in OB Golgi cells suggests that the function of these interneurons may dynamically shift from providing rhythmic potent inhibition of postsynaptic target neurons at sniffing frequencies to tonic, subtractive inhibition based on centrifugal modulatory input.
format Online
Article
Text
id pubmed-3744043
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Cold Spring Harbor Laboratory Press
record_format MEDLINE/PubMed
spelling pubmed-37440432014-09-01 Voltage-dependent intrinsic bursting in olfactory bulb Golgi cells Pressler, R. Todd Rozman, Peter A. Strowbridge, Ben W. Learn Mem Research In the mammalian olfactory bulb (OB), local synaptic circuits modulate the evolving pattern of activity in mitral and tufted cells following olfactory sensory stimulation. GABAergic granule cells, the most numerous interneuron subtype in this brain region, have been extensively studied. However, classic studies using Golgi staining methods identified many other, nongranule cell types in the OB whose function remains mysterious. Within just the granule cell layer (GCL), Ramón y Cajal described multiple morphologically distinct subtypes of nongranule interneurons including large spiny Blanes cells which exhibit intrinsic persistent activity. Here, we define the intrinsic electrophysiology of a different nongranule interneuronal cell type in the GCL described by Ramón y Cajal, sparsely spiny Golgi cells in the rat OB. Golgi cells exhibit two distinct firing modes depending on the membrane potential: tonic firing and bursting. Golgi cells also generate rebound bursts following the offset of hyperpolarizing steps. We find that both low-threshold burst responses to depolarizing inputs and rebound bursts are blocked by nickel, an antagonist of T-type voltage-gated Ca(2+) current. The state-dependent firing behavior we report in OB Golgi cells suggests that the function of these interneurons may dynamically shift from providing rhythmic potent inhibition of postsynaptic target neurons at sniffing frequencies to tonic, subtractive inhibition based on centrifugal modulatory input. Cold Spring Harbor Laboratory Press 2013-09 /pmc/articles/PMC3744043/ /pubmed/23950193 http://dx.doi.org/10.1101/lm.031856.113 Text en © 2013, Published by Cold Spring Harbor Laboratory Press http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed exclusively by Cold Spring Harbor Laboratory Press for the first 12 months after the full-issue publication date (see http://learnmem.cshlp.org/site/misc/terms.xhtml). After 12 months, it is available under a Creative Commons License (Attribution-NonCommercial 3.0 Unported), as described at http://creativecommons.org/licenses/by-nc/3.0/.
spellingShingle Research
Pressler, R. Todd
Rozman, Peter A.
Strowbridge, Ben W.
Voltage-dependent intrinsic bursting in olfactory bulb Golgi cells
title Voltage-dependent intrinsic bursting in olfactory bulb Golgi cells
title_full Voltage-dependent intrinsic bursting in olfactory bulb Golgi cells
title_fullStr Voltage-dependent intrinsic bursting in olfactory bulb Golgi cells
title_full_unstemmed Voltage-dependent intrinsic bursting in olfactory bulb Golgi cells
title_short Voltage-dependent intrinsic bursting in olfactory bulb Golgi cells
title_sort voltage-dependent intrinsic bursting in olfactory bulb golgi cells
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3744043/
https://www.ncbi.nlm.nih.gov/pubmed/23950193
http://dx.doi.org/10.1101/lm.031856.113
work_keys_str_mv AT presslerrtodd voltagedependentintrinsicburstinginolfactorybulbgolgicells
AT rozmanpetera voltagedependentintrinsicburstinginolfactorybulbgolgicells
AT strowbridgebenw voltagedependentintrinsicburstinginolfactorybulbgolgicells