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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 |
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container_title | Journal of neuroscience research |
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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. |
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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.</description><identifier>ISSN: 0360-4012</identifier><identifier>EISSN: 1097-4547</identifier><identifier>DOI: 10.1002/jnr.21068</identifier><identifier>PMID: 17006899</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>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</subject><ispartof>Journal of neuroscience research, 2006-11, Vol.84 (7), p.1425-1437</ispartof><rights>Copyright © 2006 Wiley‐Liss, Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3618-43140349e1b03c6acc0409664699e527bf1445debc6f50f46c2a666123f93ee03</citedby><cites>FETCH-LOGICAL-c3618-43140349e1b03c6acc0409664699e527bf1445debc6f50f46c2a666123f93ee03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17006899$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arias-Carrión, Oscar</creatorcontrib><creatorcontrib>Hernández-López, Salvador</creatorcontrib><creatorcontrib>Ibañez-Sandoval, Osvaldo</creatorcontrib><creatorcontrib>Bargas, José</creatorcontrib><creatorcontrib>Hernández-Cruz, Arturo</creatorcontrib><creatorcontrib>Drucker-Colín, René</creatorcontrib><title>Neuronal precursors within the adult rat subventricular zone differentiate into dopaminergic neurons after substantia nigra lesion and chromaffin cell transplant</title><title>Journal of neuroscience research</title><addtitle>J. Neurosci. Res</addtitle><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.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Behavior, Animal - drug effects</subject><subject>Brain Injuries - chemically induced</subject><subject>Brain Injuries - pathology</subject><subject>Brain Injuries - surgery</subject><subject>Cell Differentiation - physiology</subject><subject>Cerebral Ventricles - cytology</subject><subject>Cerebral Ventricles - physiology</subject><subject>Chromaffin Cells - physiology</subject><subject>Chromaffin Cells - transplantation</subject><subject>Dopamine - metabolism</subject><subject>dopaminergic neurons</subject><subject>Dose-Response Relationship, Radiation</subject><subject>Electric Stimulation</subject><subject>Immunohistochemistry - methods</subject><subject>In Vitro Techniques</subject><subject>Lysine - analogs & derivatives</subject><subject>Lysine - metabolism</subject><subject>Male</subject><subject>Membrane Potentials - physiology</subject><subject>Membrane Potentials - radiation effects</subject><subject>neurogenesis</subject><subject>Neurons - classification</subject><subject>Neurons - physiology</subject><subject>Oxidopamine</subject><subject>Parkinson's Disease model</subject><subject>Patch-Clamp Techniques - methods</subject><subject>Potassium Chloride - pharmacology</subject><subject>Rats</subject><subject>Rats, Wistar</subject><subject>Stem Cell Transplantation</subject><subject>Substantia Nigra - cytology</subject><subject>Substantia Nigra - physiology</subject><subject>Substantia Nigra - transplantation</subject><subject>substantia nigra lesion</subject><subject>Tyrosine 3-Monooxygenase - metabolism</subject><issn>0360-4012</issn><issn>1097-4547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp1kMFu1DAQQC0EotvCgR9AvnJIO44dpz6iFgqoXSQE2qPlOOOuS9ZZjR1K-Zv-KdlugROnkUZv3kiPsVcCjgVAfXKT6LgWoE-fsIUA01aqUe1TtgCpoVIg6gN2mPMNABjTyOfsQLQw08Ys2P0SJxqTG_iW0E-UR8r8NpZ1TLyskbt-GgonV3ieuh-YCkU_DY74rzEh72MISPM2uoI8pjLyfty6TUxI19Hz9CDP3IWCtDPk4nYwT_GaHB8wxzFxl3ru1zRuXAjzW4_DwAu5lLfDTL9gz4IbMr58nEfs2_t3X88-VJefLz6evb2svNTitFJSKJDKoOhAeu28BwVGa6WNwaZuuyCUanrsvA4NBKV97bTWopbBSESQR-zN3utpzJkw2C3FjaM7K8DuMts5s33IPLOv9-x26jbY_yMfu87AyR64jQPe_d9kPy2__FFW-4uYC_78e-Hou9WtbBu7Wl7Yq6tmda5W57aRvwFB5JsH</recordid><startdate>20061115</startdate><enddate>20061115</enddate><creator>Arias-Carrión, Oscar</creator><creator>Hernández-López, Salvador</creator><creator>Ibañez-Sandoval, Osvaldo</creator><creator>Bargas, José</creator><creator>Hernández-Cruz, Arturo</creator><creator>Drucker-Colín, René</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20061115</creationdate><title>Neuronal precursors within the adult rat subventricular zone differentiate into dopaminergic neurons after substantia nigra lesion and chromaffin cell transplant</title><author>Arias-Carrión, Oscar ; Hernández-López, Salvador ; Ibañez-Sandoval, Osvaldo ; Bargas, José ; Hernández-Cruz, Arturo ; Drucker-Colín, René</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3618-43140349e1b03c6acc0409664699e527bf1445debc6f50f46c2a666123f93ee03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Behavior, Animal - drug effects</topic><topic>Brain Injuries - chemically induced</topic><topic>Brain Injuries - pathology</topic><topic>Brain Injuries - surgery</topic><topic>Cell Differentiation - physiology</topic><topic>Cerebral Ventricles - cytology</topic><topic>Cerebral Ventricles - physiology</topic><topic>Chromaffin Cells - physiology</topic><topic>Chromaffin Cells - transplantation</topic><topic>Dopamine - metabolism</topic><topic>dopaminergic neurons</topic><topic>Dose-Response Relationship, Radiation</topic><topic>Electric Stimulation</topic><topic>Immunohistochemistry - methods</topic><topic>In Vitro Techniques</topic><topic>Lysine - analogs & derivatives</topic><topic>Lysine - metabolism</topic><topic>Male</topic><topic>Membrane Potentials - physiology</topic><topic>Membrane Potentials - radiation effects</topic><topic>neurogenesis</topic><topic>Neurons - classification</topic><topic>Neurons - physiology</topic><topic>Oxidopamine</topic><topic>Parkinson's Disease model</topic><topic>Patch-Clamp Techniques - methods</topic><topic>Potassium Chloride - pharmacology</topic><topic>Rats</topic><topic>Rats, Wistar</topic><topic>Stem Cell Transplantation</topic><topic>Substantia Nigra - cytology</topic><topic>Substantia Nigra - physiology</topic><topic>Substantia Nigra - transplantation</topic><topic>substantia nigra lesion</topic><topic>Tyrosine 3-Monooxygenase - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Arias-Carrión, Oscar</creatorcontrib><creatorcontrib>Hernández-López, Salvador</creatorcontrib><creatorcontrib>Ibañez-Sandoval, Osvaldo</creatorcontrib><creatorcontrib>Bargas, José</creatorcontrib><creatorcontrib>Hernández-Cruz, Arturo</creatorcontrib><creatorcontrib>Drucker-Colín, René</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Journal of neuroscience research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arias-Carrión, Oscar</au><au>Hernández-López, Salvador</au><au>Ibañez-Sandoval, Osvaldo</au><au>Bargas, José</au><au>Hernández-Cruz, Arturo</au><au>Drucker-Colín, René</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Neuronal precursors within the adult rat subventricular zone differentiate into dopaminergic neurons after substantia nigra lesion and chromaffin cell transplant</atitle><jtitle>Journal of neuroscience research</jtitle><addtitle>J. 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. 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.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>17006899</pmid><doi>10.1002/jnr.21068</doi><tpages>13</tpages></addata></record> |
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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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