Midbrain dopaminergic neurons generate calcium and sodium currents and release dopamine in the striatum of pups

Midbrain dopaminergic neurons (mDA neurons) are essential for the control of diverse motor and cognitive behaviors. However, our understanding of the activity of immature mDA neurons is rudimentary. Rodent mDA neurons migrate and differentiate early in embryonic life and dopaminergic axons enter the...

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Main Authors: Diana Carolina Ferrari, Baya Julius Mdzomba, Nathalie eDehorter, Catherine eLopez, François Jérôme Michel, Frédéric eLibersat, Constance eHammond
Format: Article
Language:English
Published: Frontiers Media S.A. 2012-03-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fncel.2012.00007/full
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author Diana Carolina Ferrari
Baya Julius Mdzomba
Nathalie eDehorter
Catherine eLopez
François Jérôme Michel
Frédéric eLibersat
Constance eHammond
author_facet Diana Carolina Ferrari
Baya Julius Mdzomba
Nathalie eDehorter
Catherine eLopez
François Jérôme Michel
Frédéric eLibersat
Constance eHammond
author_sort Diana Carolina Ferrari
collection DOAJ
description Midbrain dopaminergic neurons (mDA neurons) are essential for the control of diverse motor and cognitive behaviors. However, our understanding of the activity of immature mDA neurons is rudimentary. Rodent mDA neurons migrate and differentiate early in embryonic life and dopaminergic axons enter the striatum and contact striatal neurons a few days before birth, but when these are functional is not known. Here, we recorded Ca2+ transients and Na+ spikes from embryonic (E16-E18) and early postnatal (P0-P7) mDA neurons with dynamic two photon imaging and patch clamp techniques in slices from tyrosine hydroxylase-GFP mice, and measured evoked dopamine release in the striatum with amperometry. We show that half of identified E16-P0 mDA neurons spontaneously generate non-synaptic, intrinsically-driven Ca2+ spikes and Ca2+ plateaus mediated by N- and L-type voltage-gated Ca2+ channels. Starting from E18-P0, half of the mDA neurons also reliably generate overshooting Na+ spikes with an abrupt maturation at birth (P0 = E19). At that stage (E18-P0), dopaminergic terminals release dopamine in a calcium-dependent manner in the striatum in response to local stimulation. We propose that the intrinsic spontaneous activity of mouse mDA neurons may impact the development/activity of the striatal network from birth.
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spelling doaj.art-6c7d0aa7e3d94e6999c5916293aa0e282022-12-22T02:31:39ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022012-03-01610.3389/fncel.2012.0000720947Midbrain dopaminergic neurons generate calcium and sodium currents and release dopamine in the striatum of pupsDiana Carolina Ferrari0Baya Julius Mdzomba1Nathalie eDehorter2Catherine eLopez3François Jérôme Michel4Frédéric eLibersat5Constance eHammond6Institut national de la Recherche Médicale et de la Santé InsermInstitut national de la Recherche Médicale et de la Santé InsermInstitut national de la Recherche Médicale et de la Santé InsermInstitut national de la Recherche Médicale et de la Santé InsermInstitut national de la Recherche Médicale et de la Santé InsermInstitut national de la Recherche Médicale et de la Santé InsermInstitut national de la Recherche Médicale et de la Santé InsermMidbrain dopaminergic neurons (mDA neurons) are essential for the control of diverse motor and cognitive behaviors. However, our understanding of the activity of immature mDA neurons is rudimentary. Rodent mDA neurons migrate and differentiate early in embryonic life and dopaminergic axons enter the striatum and contact striatal neurons a few days before birth, but when these are functional is not known. Here, we recorded Ca2+ transients and Na+ spikes from embryonic (E16-E18) and early postnatal (P0-P7) mDA neurons with dynamic two photon imaging and patch clamp techniques in slices from tyrosine hydroxylase-GFP mice, and measured evoked dopamine release in the striatum with amperometry. We show that half of identified E16-P0 mDA neurons spontaneously generate non-synaptic, intrinsically-driven Ca2+ spikes and Ca2+ plateaus mediated by N- and L-type voltage-gated Ca2+ channels. Starting from E18-P0, half of the mDA neurons also reliably generate overshooting Na+ spikes with an abrupt maturation at birth (P0 = E19). At that stage (E18-P0), dopaminergic terminals release dopamine in a calcium-dependent manner in the striatum in response to local stimulation. We propose that the intrinsic spontaneous activity of mouse mDA neurons may impact the development/activity of the striatal network from birth.http://journal.frontiersin.org/Journal/10.3389/fncel.2012.00007/fullBasal GangliaDopamineSubstantia Nigradevelopmentpatch clampimmature activity
spellingShingle Diana Carolina Ferrari
Baya Julius Mdzomba
Nathalie eDehorter
Catherine eLopez
François Jérôme Michel
Frédéric eLibersat
Constance eHammond
Midbrain dopaminergic neurons generate calcium and sodium currents and release dopamine in the striatum of pups
Frontiers in Cellular Neuroscience
Basal Ganglia
Dopamine
Substantia Nigra
development
patch clamp
immature activity
title Midbrain dopaminergic neurons generate calcium and sodium currents and release dopamine in the striatum of pups
title_full Midbrain dopaminergic neurons generate calcium and sodium currents and release dopamine in the striatum of pups
title_fullStr Midbrain dopaminergic neurons generate calcium and sodium currents and release dopamine in the striatum of pups
title_full_unstemmed Midbrain dopaminergic neurons generate calcium and sodium currents and release dopamine in the striatum of pups
title_short Midbrain dopaminergic neurons generate calcium and sodium currents and release dopamine in the striatum of pups
title_sort midbrain dopaminergic neurons generate calcium and sodium currents and release dopamine in the striatum of pups
topic Basal Ganglia
Dopamine
Substantia Nigra
development
patch clamp
immature activity
url http://journal.frontiersin.org/Journal/10.3389/fncel.2012.00007/full
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