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Neuronal precursors within the adult rat subventricular zone differentiate into dopaminergic neurons after substantia nigra lesion and chromaffin cell transplant

Neurogenesis in the adult mammalian brain continues in the subventricular zone (SVZ). Neuronal precursors from the SVZ migrate along the rostral migratory stream to replace olfactory bulb interneurons. After the destruction of the nigro‐striatal pathway (SN‐lesion), some SVZ precursors begin to expr...

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Published in:Journal of neuroscience research 2006-11, Vol.84 (7), p.1425-1437
Main Authors: Arias-Carrión, Oscar, Hernández-López, Salvador, Ibañez-Sandoval, Osvaldo, Bargas, José, Hernández-Cruz, Arturo, Drucker-Colín, René
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cited_by cdi_FETCH-LOGICAL-c3618-43140349e1b03c6acc0409664699e527bf1445debc6f50f46c2a666123f93ee03
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container_issue 7
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container_title Journal of neuroscience research
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creator Arias-Carrión, Oscar
Hernández-López, Salvador
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Drucker-Colín, René
description Neurogenesis in the adult mammalian brain continues in the subventricular zone (SVZ). Neuronal precursors from the SVZ migrate along the rostral migratory stream to replace olfactory bulb interneurons. After the destruction of the nigro‐striatal pathway (SN‐lesion), some SVZ precursors begin to express tyrosine hydroxylase (TH) and neuronal markers (NeuN). Grafting of chromaffin cells (CCs) into the denervated striatum increases the number of TH+ cells (SVZ TH+ cells; Arias‐Carrión et al., 2004). This study examines the functional properties of these newly differentiating TH+ cells. Under whole‐cell patch‐clamp, most SVZ cells recorded from lesioned and grafted animals (either TH+ or TH−) were non‐excitable. Nevertheless, a small percentage of SVZ TH+ cells had the electrophysiologic phenotype of mature dopaminergic neurons and showed spontaneous postsynaptic potentials. Dopamine (DA) release was measured in SVZ and striatum from both control and SN‐lesioned rats. As expected, 12 weeks after SN lesion, DA release decreased drastically. Nevertheless, 8 weeks after CCs graft, release from the SVZ of SN‐lesioned rats recovered, and even surpassed that from control SVZ, suggesting that newly formed SVZ TH+ cells release DA. This study shows for the first time that in response to SN‐lesions and CC grafts neural precursors within the SVZ change their developmental program, by not only expressing TH, but more importantly by acquiring excitable properties of mature dopaminergic neurons. Additionally, the release of DA in a Ca2+‐dependent manner and the attraction of synaptic afferents from neighboring neuronal networks gives further significance to the overall findings, whose potential importance is discussed. © 2006 Wiley‐Liss, Inc.
doi_str_mv 10.1002/jnr.21068
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Dopamine (DA) release was measured in SVZ and striatum from both control and SN‐lesioned rats. As expected, 12 weeks after SN lesion, DA release decreased drastically. Nevertheless, 8 weeks after CCs graft, release from the SVZ of SN‐lesioned rats recovered, and even surpassed that from control SVZ, suggesting that newly formed SVZ TH+ cells release DA. This study shows for the first time that in response to SN‐lesions and CC grafts neural precursors within the SVZ change their developmental program, by not only expressing TH, but more importantly by acquiring excitable properties of mature dopaminergic neurons. 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Neurosci. Res</addtitle><date>2006-11-15</date><risdate>2006</risdate><volume>84</volume><issue>7</issue><spage>1425</spage><epage>1437</epage><pages>1425-1437</pages><issn>0360-4012</issn><eissn>1097-4547</eissn><abstract>Neurogenesis in the adult mammalian brain continues in the subventricular zone (SVZ). Neuronal precursors from the SVZ migrate along the rostral migratory stream to replace olfactory bulb interneurons. After the destruction of the nigro‐striatal pathway (SN‐lesion), some SVZ precursors begin to express tyrosine hydroxylase (TH) and neuronal markers (NeuN). Grafting of chromaffin cells (CCs) into the denervated striatum increases the number of TH+ cells (SVZ TH+ cells; Arias‐Carrión et al., 2004). This study examines the functional properties of these newly differentiating TH+ cells. Under whole‐cell patch‐clamp, most SVZ cells recorded from lesioned and grafted animals (either TH+ or TH−) were non‐excitable. Nevertheless, a small percentage of SVZ TH+ cells had the electrophysiologic phenotype of mature dopaminergic neurons and showed spontaneous postsynaptic potentials. Dopamine (DA) release was measured in SVZ and striatum from both control and SN‐lesioned rats. As expected, 12 weeks after SN lesion, DA release decreased drastically. Nevertheless, 8 weeks after CCs graft, release from the SVZ of SN‐lesioned rats recovered, and even surpassed that from control SVZ, suggesting that newly formed SVZ TH+ cells release DA. This study shows for the first time that in response to SN‐lesions and CC grafts neural precursors within the SVZ change their developmental program, by not only expressing TH, but more importantly by acquiring excitable properties of mature dopaminergic neurons. 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subjects Analysis of Variance
Animals
Behavior, Animal - drug effects
Brain Injuries - chemically induced
Brain Injuries - pathology
Brain Injuries - surgery
Cell Differentiation - physiology
Cerebral Ventricles - cytology
Cerebral Ventricles - physiology
Chromaffin Cells - physiology
Chromaffin Cells - transplantation
Dopamine - metabolism
dopaminergic neurons
Dose-Response Relationship, Radiation
Electric Stimulation
Immunohistochemistry - methods
In Vitro Techniques
Lysine - analogs & derivatives
Lysine - metabolism
Male
Membrane Potentials - physiology
Membrane Potentials - radiation effects
neurogenesis
Neurons - classification
Neurons - physiology
Oxidopamine
Parkinson's Disease model
Patch-Clamp Techniques - methods
Potassium Chloride - pharmacology
Rats
Rats, Wistar
Stem Cell Transplantation
Substantia Nigra - cytology
Substantia Nigra - physiology
Substantia Nigra - transplantation
substantia nigra lesion
Tyrosine 3-Monooxygenase - metabolism
title Neuronal precursors within the adult rat subventricular zone differentiate into dopaminergic neurons after substantia nigra lesion and chromaffin cell transplant
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