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Adult subventricular zone neural stem cells as a potential source of dopaminergic replacement neurons
Clinical trials engrafting human fetal ventral mesencephalic tissue have demonstrated, in principle, that cell replacement therapy provides substantial long-lasting improvement of motor impairments generated by Parkinson's Disease (PD). The use of fetal tissue is not practical for widespread cl...
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Published in: | Frontiers in neuroscience 2014-02, Vol.8, p.16-16 |
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description | Clinical trials engrafting human fetal ventral mesencephalic tissue have demonstrated, in principle, that cell replacement therapy provides substantial long-lasting improvement of motor impairments generated by Parkinson's Disease (PD). The use of fetal tissue is not practical for widespread clinical implementation of this therapy, but stem cells are a promising alternative source for obtaining replacement cells. The ideal stem cell source has yet to be established and, in this review, we discuss the potential of neural stem cells in the adult subventricular zone (SVZ) as an autologous source of replacement cells. We identify three key challenges for further developing this potential source of replacement cells: (1) improving survival of transplanted cells, (2) suppressing glial progenitor proliferation and survival, and (3) developing methods to efficiently produce dopaminergic neurons. Subventricular neural stem cells naturally produce a dopaminergic interneuron phenotype that has an apparent lack of vulnerability to PD-mediated degeneration. We also discuss whether olfactory bulb dopaminergic neurons derived from adult SVZ neural stem cells are a suitable source for cell replacement strategies. |
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The use of fetal tissue is not practical for widespread clinical implementation of this therapy, but stem cells are a promising alternative source for obtaining replacement cells. The ideal stem cell source has yet to be established and, in this review, we discuss the potential of neural stem cells in the adult subventricular zone (SVZ) as an autologous source of replacement cells. We identify three key challenges for further developing this potential source of replacement cells: (1) improving survival of transplanted cells, (2) suppressing glial progenitor proliferation and survival, and (3) developing methods to efficiently produce dopaminergic neurons. Subventricular neural stem cells naturally produce a dopaminergic interneuron phenotype that has an apparent lack of vulnerability to PD-mediated degeneration. We also discuss whether olfactory bulb dopaminergic neurons derived from adult SVZ neural stem cells are a suitable source for cell replacement strategies.</description><identifier>ISSN: 1662-4548</identifier><identifier>ISSN: 1662-453X</identifier><identifier>EISSN: 1662-453X</identifier><identifier>DOI: 10.3389/fnins.2014.00016</identifier><identifier>PMID: 24574954</identifier><language>eng</language><publisher>Switzerland: Frontiers Research Foundation</publisher><subject>adult neurogenesis ; Autografts ; Cell proliferation ; cell replacement therapy ; Clinical trials ; Degeneration ; Dopamine ; Dopamine receptors ; dopaminergic ; Embryos ; Fetuses ; Movement disorders ; Neural Stem Cells ; Neurodegenerative diseases ; Neuroscience ; Olfactory Bulb ; Parkinson's disease ; Phenotypes ; Stem cells ; Subventricular zone</subject><ispartof>Frontiers in neuroscience, 2014-02, Vol.8, p.16-16</ispartof><rights>2014. 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Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>Copyright © 2014 Cave, Wang and Baker. 2014</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c523t-ff060adfa2b2161c489219752262250c6b8d7a3600faeb8d58dc5a39f05baf863</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2304982973/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2304982973?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25732,27903,27904,36991,36992,44569,53769,53771,74872</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24574954$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cave, John W</creatorcontrib><creatorcontrib>Wang, Meng</creatorcontrib><creatorcontrib>Baker, Harriet</creatorcontrib><title>Adult subventricular zone neural stem cells as a potential source of dopaminergic replacement neurons</title><title>Frontiers in neuroscience</title><addtitle>Front Neurosci</addtitle><description>Clinical trials engrafting human fetal ventral mesencephalic tissue have demonstrated, in principle, that cell replacement therapy provides substantial long-lasting improvement of motor impairments generated by Parkinson's Disease (PD). 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We also discuss whether olfactory bulb dopaminergic neurons derived from adult SVZ neural stem cells are a suitable source for cell replacement strategies.</description><subject>adult neurogenesis</subject><subject>Autografts</subject><subject>Cell proliferation</subject><subject>cell replacement therapy</subject><subject>Clinical trials</subject><subject>Degeneration</subject><subject>Dopamine</subject><subject>Dopamine receptors</subject><subject>dopaminergic</subject><subject>Embryos</subject><subject>Fetuses</subject><subject>Movement disorders</subject><subject>Neural Stem Cells</subject><subject>Neurodegenerative diseases</subject><subject>Neuroscience</subject><subject>Olfactory Bulb</subject><subject>Parkinson's disease</subject><subject>Phenotypes</subject><subject>Stem cells</subject><subject>Subventricular zone</subject><issn>1662-4548</issn><issn>1662-453X</issn><issn>1662-453X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNks9rFDEUxwdRbK3ePUnAi5dd83uSi1CK2kLBi4K38CaTrFlmkjGZKehfb2a3Lq0nIZCQ93lfku_7Ns1rgreMKf3exxDLlmLCtxhjIp8050RKuuGCfX96OnN11rwoZY-xpIrT580Z5aLlWvDzxl32yzCjsnR3Ls452GWAjH6n6FB0S4YBldmNyLphKAjqQlOaKxnWSlqydSh51KcJxhBd3gWLspsGsG6s1EEjxfKyeeZhKO7V_X7RfPv08evV9eb2y-ebq8vbjRWUzRvvscTQe6AdJZJYrjQluhWUSkoFtrJTfQtMYuzB1bNQvRXAtMeiA68ku2hujrp9gr2Zchgh_zIJgjlcpLwzkOdgB2e86mzHQTNQhFtmtRYat2A7T7z0mFatD0etaelG19vVHhgeiT6uxPDD7NKdYZooKXAVeHcvkNPPxZXZjKGsRkJ0aSmGCI5JnR0R_4EyrqoLLano23_QfR1DrK4ayjDXiuqWVQofKZtTKdn507sJNmt0zCE6Zo2OOUSntrx5-N9Tw9-ssD-1LMIH</recordid><startdate>20140210</startdate><enddate>20140210</enddate><creator>Cave, John W</creator><creator>Wang, Meng</creator><creator>Baker, Harriet</creator><general>Frontiers Research Foundation</general><general>Frontiers Media S.A</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>88I</scope><scope>8FE</scope><scope>8FH</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>LK8</scope><scope>M2P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7TK</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>20140210</creationdate><title>Adult subventricular zone neural stem cells as a potential source of dopaminergic replacement neurons</title><author>Cave, John W ; Wang, Meng ; Baker, Harriet</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c523t-ff060adfa2b2161c489219752262250c6b8d7a3600faeb8d58dc5a39f05baf863</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>adult neurogenesis</topic><topic>Autografts</topic><topic>Cell proliferation</topic><topic>cell replacement therapy</topic><topic>Clinical trials</topic><topic>Degeneration</topic><topic>Dopamine</topic><topic>Dopamine receptors</topic><topic>dopaminergic</topic><topic>Embryos</topic><topic>Fetuses</topic><topic>Movement disorders</topic><topic>Neural Stem Cells</topic><topic>Neurodegenerative diseases</topic><topic>Neuroscience</topic><topic>Olfactory Bulb</topic><topic>Parkinson's disease</topic><topic>Phenotypes</topic><topic>Stem cells</topic><topic>Subventricular zone</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cave, John W</creatorcontrib><creatorcontrib>Wang, Meng</creatorcontrib><creatorcontrib>Baker, Harriet</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Science Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Biological Science Collection</collection><collection>Science Database</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Frontiers in neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cave, John W</au><au>Wang, Meng</au><au>Baker, Harriet</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Adult subventricular zone neural stem cells as a potential source of dopaminergic replacement neurons</atitle><jtitle>Frontiers in neuroscience</jtitle><addtitle>Front Neurosci</addtitle><date>2014-02-10</date><risdate>2014</risdate><volume>8</volume><spage>16</spage><epage>16</epage><pages>16-16</pages><issn>1662-4548</issn><issn>1662-453X</issn><eissn>1662-453X</eissn><abstract>Clinical trials engrafting human fetal ventral mesencephalic tissue have demonstrated, in principle, that cell replacement therapy provides substantial long-lasting improvement of motor impairments generated by Parkinson's Disease (PD). 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subjects | adult neurogenesis Autografts Cell proliferation cell replacement therapy Clinical trials Degeneration Dopamine Dopamine receptors dopaminergic Embryos Fetuses Movement disorders Neural Stem Cells Neurodegenerative diseases Neuroscience Olfactory Bulb Parkinson's disease Phenotypes Stem cells Subventricular zone |
title | Adult subventricular zone neural stem cells as a potential source of dopaminergic replacement neurons |
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