Experimental and clinical factors influencing long-term stable in vitro expansion of multipotent neural cells from human adult temporal lobes
Autologous adult human neural stem cells may be used for regenerative cell therapies bypass potential ethical problems. However, stable in vitro expansion protocols and experimental/clinical factors influencing primary cultures need to be further elucidated for clinically applicable techniques. To a...
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Veröffentlicht in: | Experimental neurology 2013-02, Vol.240, p.168-177 |
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container_title | Experimental neurology |
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creator | Joo, Kyeung Min Kang, Bong Gu Yeon, Je Young Cho, Yu Jin An, Jae Yeol Song, Hyeon Suk Won, Jun Ho Kim, Sang Jeong Hong, Seung-Chyul Nam, Do-Hyun |
description | Autologous adult human neural stem cells may be used for regenerative cell therapies bypass potential ethical problems. However, stable in vitro expansion protocols and experimental/clinical factors influencing primary cultures need to be further elucidated for clinically applicable techniques. To address these issues, we obtained biopsy specimens from 23 temporal lobe epilepsy patients and adult human multipotent neural cells (ahMNCs) were primarily cultured in a defined attachment culture condition. When the success of primary cultures was defined as stable expansion of cells (>ten in vitro passages) and expression of NSC markers, success rate of the primary culture was 39% (nine of 23 temporal lobes). During the long-term expansion, expressions of NSC markers and differentiation potentials into astrocytes and neurons were maintained. After the 18th sub-culture, spontaneous senescence and differentiation were observed, and the cultivated ahMNCs ceased their proliferation. The culture results were not affected by seizure characteristics; however, an older age (>40years) and a smaller sample volume ( |
doi_str_mv | 10.1016/j.expneurol.2012.11.021 |
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► Multipotent neural cells were cultured from the human adult temporal lobe. ► In the attachment culture condition, the cells were stably expanded. ► The cells expressed neural stem cell markers and showed differentiation potentials. ► Surgical sample volume and age affected the success of the primary culture. ► Implantation of the cells had significant therapeutic effects against the stroke.</description><identifier>ISSN: 0014-4886</identifier><identifier>EISSN: 1090-2430</identifier><identifier>DOI: 10.1016/j.expneurol.2012.11.021</identifier><identifier>PMID: 23201097</identifier><identifier>CODEN: EXNEAC</identifier><language>eng</language><publisher>Amsterdam: Elsevier Inc</publisher><subject>Adolescent ; Adult ; Adult human brain ; Adult Stem Cells - cytology ; Adult Stem Cells - transplantation ; Animals ; Biological and medical sciences ; Child ; Disease Models, Animal ; Epilepsy, Temporal Lobe - physiopathology ; Experimental and clinical factors ; Female ; Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy ; Humans ; In vitro expansion ; Infarction, Middle Cerebral Artery - therapy ; Male ; Medical sciences ; Middle Aged ; Multipotent neural cells ; Multipotent Stem Cells - cytology ; Multipotent Stem Cells - transplantation ; Nervous system (semeiology, syndromes) ; Neural Stem Cells - cytology ; Neural Stem Cells - transplantation ; Neurology ; Primary Cell Culture - methods ; Random Allocation ; Rats ; Rats, Sprague-Dawley ; Stroke ; Temporal Lobe - cytology ; Temporal lobe epilepsy ; Therapeutic effects ; Young Adult</subject><ispartof>Experimental neurology, 2013-02, Vol.240, p.168-177</ispartof><rights>2012 Elsevier Inc.</rights><rights>2014 INIST-CNRS</rights><rights>Copyright © 2012 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c467t-92fd40574fea131678c098971f9a16e93a495b0647e6956abbe5c086051f24f03</citedby><cites>FETCH-LOGICAL-c467t-92fd40574fea131678c098971f9a16e93a495b0647e6956abbe5c086051f24f03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.expneurol.2012.11.021$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3537,27905,27906,45976</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=26898269$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23201097$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Joo, Kyeung Min</creatorcontrib><creatorcontrib>Kang, Bong Gu</creatorcontrib><creatorcontrib>Yeon, Je Young</creatorcontrib><creatorcontrib>Cho, Yu Jin</creatorcontrib><creatorcontrib>An, Jae Yeol</creatorcontrib><creatorcontrib>Song, Hyeon Suk</creatorcontrib><creatorcontrib>Won, Jun Ho</creatorcontrib><creatorcontrib>Kim, Sang Jeong</creatorcontrib><creatorcontrib>Hong, Seung-Chyul</creatorcontrib><creatorcontrib>Nam, Do-Hyun</creatorcontrib><title>Experimental and clinical factors influencing long-term stable in vitro expansion of multipotent neural cells from human adult temporal lobes</title><title>Experimental neurology</title><addtitle>Exp Neurol</addtitle><description>Autologous adult human neural stem cells may be used for regenerative cell therapies bypass potential ethical problems. However, stable in vitro expansion protocols and experimental/clinical factors influencing primary cultures need to be further elucidated for clinically applicable techniques. To address these issues, we obtained biopsy specimens from 23 temporal lobe epilepsy patients and adult human multipotent neural cells (ahMNCs) were primarily cultured in a defined attachment culture condition. When the success of primary cultures was defined as stable expansion of cells (>ten in vitro passages) and expression of NSC markers, success rate of the primary culture was 39% (nine of 23 temporal lobes). During the long-term expansion, expressions of NSC markers and differentiation potentials into astrocytes and neurons were maintained. After the 18th sub-culture, spontaneous senescence and differentiation were observed, and the cultivated ahMNCs ceased their proliferation. The culture results were not affected by seizure characteristics; however, an older age (>40years) and a smaller sample volume (<2ml) were found to exert negative influences on the primary culture results. Furthermore therapeutic effects of ahMNCs against stroke were analyzed in an animal model. Transplantation of ahMNCs cells reduced infarction volumes and enhanced motor activity, significantly. The results here would provide promising experimental and clinical strategy of using patient-specific autologous ahMNCs in regenerative medicine in the future.
► Multipotent neural cells were cultured from the human adult temporal lobe. ► In the attachment culture condition, the cells were stably expanded. ► The cells expressed neural stem cell markers and showed differentiation potentials. ► Surgical sample volume and age affected the success of the primary culture. ► Implantation of the cells had significant therapeutic effects against the stroke.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Adult human brain</subject><subject>Adult Stem Cells - cytology</subject><subject>Adult Stem Cells - transplantation</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Disease Models, Animal</subject><subject>Epilepsy, Temporal Lobe - physiopathology</subject><subject>Experimental and clinical factors</subject><subject>Female</subject><subject>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</subject><subject>Humans</subject><subject>In vitro expansion</subject><subject>Infarction, Middle Cerebral Artery - therapy</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Multipotent neural cells</subject><subject>Multipotent Stem Cells - cytology</subject><subject>Multipotent Stem Cells - transplantation</subject><subject>Nervous system (semeiology, syndromes)</subject><subject>Neural Stem Cells - cytology</subject><subject>Neural Stem Cells - transplantation</subject><subject>Neurology</subject><subject>Primary Cell Culture - methods</subject><subject>Random Allocation</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Stroke</subject><subject>Temporal Lobe - cytology</subject><subject>Temporal lobe epilepsy</subject><subject>Therapeutic effects</subject><subject>Young Adult</subject><issn>0014-4886</issn><issn>1090-2430</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU-P1SAUxYnROM_Rr6BsTNy0AqW0LCeT8U8yiRtdE0ovIy8UKtDJ-CHmO0vznuNSNoTc37mcnIPQO0paSqj4eGzhYQ2wpehbRihrKW0Jo8_QgRJJGsY78hwdCKG84eMoLtCrnI-EEMnZ8BJdsK6KiBwO6PHmYYXkFghFe6zDjI13wZn6sNqUmDJ2wfoNgnHhDvsY7poCacG56MlDHeJ7V1LE1Y8O2cWAo8XL5otbY6lb8e6ybjPgfcY2xQX_3BYdsJ4rhAssa9znPk6QX6MXVvsMb873Jfrx6eb79Zfm9tvnr9dXt43hYiiNZHbmpB-4BU07KobREDnKgVqpqQDZaS77iQg-gJC90NMEvSGjID21jFvSXaIPp71rir82yEUtLu8OdYC4ZUXZ0A31sB0dTqhJMecEVq01Lp1-K0rU3oU6qqcu1N6FolTVLqry7fmTbVpgftL9Db8C78-AzjVwm3QNOf_jxChHJmTlrk4c1EjuHSSVjauFwOwSmKLm6P5r5g9VJ68H</recordid><startdate>20130201</startdate><enddate>20130201</enddate><creator>Joo, Kyeung Min</creator><creator>Kang, Bong Gu</creator><creator>Yeon, Je Young</creator><creator>Cho, Yu Jin</creator><creator>An, Jae Yeol</creator><creator>Song, Hyeon Suk</creator><creator>Won, Jun Ho</creator><creator>Kim, Sang Jeong</creator><creator>Hong, Seung-Chyul</creator><creator>Nam, Do-Hyun</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>IQODW</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><scope>7X8</scope></search><sort><creationdate>20130201</creationdate><title>Experimental and clinical factors influencing long-term stable in vitro expansion of multipotent neural cells from human adult temporal lobes</title><author>Joo, Kyeung Min ; Kang, Bong Gu ; Yeon, Je Young ; Cho, Yu Jin ; An, Jae Yeol ; Song, Hyeon Suk ; Won, Jun Ho ; Kim, Sang Jeong ; Hong, Seung-Chyul ; Nam, Do-Hyun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c467t-92fd40574fea131678c098971f9a16e93a495b0647e6956abbe5c086051f24f03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Adult human brain</topic><topic>Adult Stem Cells - cytology</topic><topic>Adult Stem Cells - transplantation</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Disease Models, Animal</topic><topic>Epilepsy, Temporal Lobe - physiopathology</topic><topic>Experimental and clinical factors</topic><topic>Female</topic><topic>Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy</topic><topic>Humans</topic><topic>In vitro expansion</topic><topic>Infarction, Middle Cerebral Artery - therapy</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Multipotent neural cells</topic><topic>Multipotent Stem Cells - cytology</topic><topic>Multipotent Stem Cells - transplantation</topic><topic>Nervous system (semeiology, syndromes)</topic><topic>Neural Stem Cells - cytology</topic><topic>Neural Stem Cells - transplantation</topic><topic>Neurology</topic><topic>Primary Cell Culture - methods</topic><topic>Random Allocation</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Stroke</topic><topic>Temporal Lobe - cytology</topic><topic>Temporal lobe epilepsy</topic><topic>Therapeutic effects</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Joo, Kyeung Min</creatorcontrib><creatorcontrib>Kang, Bong Gu</creatorcontrib><creatorcontrib>Yeon, Je Young</creatorcontrib><creatorcontrib>Cho, Yu Jin</creatorcontrib><creatorcontrib>An, Jae Yeol</creatorcontrib><creatorcontrib>Song, Hyeon Suk</creatorcontrib><creatorcontrib>Won, Jun Ho</creatorcontrib><creatorcontrib>Kim, Sang Jeong</creatorcontrib><creatorcontrib>Hong, Seung-Chyul</creatorcontrib><creatorcontrib>Nam, Do-Hyun</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Experimental neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Joo, Kyeung Min</au><au>Kang, Bong Gu</au><au>Yeon, Je Young</au><au>Cho, Yu Jin</au><au>An, Jae Yeol</au><au>Song, Hyeon Suk</au><au>Won, Jun Ho</au><au>Kim, Sang Jeong</au><au>Hong, Seung-Chyul</au><au>Nam, Do-Hyun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Experimental and clinical factors influencing long-term stable in vitro expansion of multipotent neural cells from human adult temporal lobes</atitle><jtitle>Experimental neurology</jtitle><addtitle>Exp Neurol</addtitle><date>2013-02-01</date><risdate>2013</risdate><volume>240</volume><spage>168</spage><epage>177</epage><pages>168-177</pages><issn>0014-4886</issn><eissn>1090-2430</eissn><coden>EXNEAC</coden><abstract>Autologous adult human neural stem cells may be used for regenerative cell therapies bypass potential ethical problems. However, stable in vitro expansion protocols and experimental/clinical factors influencing primary cultures need to be further elucidated for clinically applicable techniques. To address these issues, we obtained biopsy specimens from 23 temporal lobe epilepsy patients and adult human multipotent neural cells (ahMNCs) were primarily cultured in a defined attachment culture condition. When the success of primary cultures was defined as stable expansion of cells (>ten in vitro passages) and expression of NSC markers, success rate of the primary culture was 39% (nine of 23 temporal lobes). During the long-term expansion, expressions of NSC markers and differentiation potentials into astrocytes and neurons were maintained. After the 18th sub-culture, spontaneous senescence and differentiation were observed, and the cultivated ahMNCs ceased their proliferation. The culture results were not affected by seizure characteristics; however, an older age (>40years) and a smaller sample volume (<2ml) were found to exert negative influences on the primary culture results. Furthermore therapeutic effects of ahMNCs against stroke were analyzed in an animal model. Transplantation of ahMNCs cells reduced infarction volumes and enhanced motor activity, significantly. The results here would provide promising experimental and clinical strategy of using patient-specific autologous ahMNCs in regenerative medicine in the future.
► Multipotent neural cells were cultured from the human adult temporal lobe. ► In the attachment culture condition, the cells were stably expanded. ► The cells expressed neural stem cell markers and showed differentiation potentials. ► Surgical sample volume and age affected the success of the primary culture. ► Implantation of the cells had significant therapeutic effects against the stroke.</abstract><cop>Amsterdam</cop><pub>Elsevier Inc</pub><pmid>23201097</pmid><doi>10.1016/j.expneurol.2012.11.021</doi><tpages>10</tpages></addata></record> |
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subjects | Adolescent Adult Adult human brain Adult Stem Cells - cytology Adult Stem Cells - transplantation Animals Biological and medical sciences Child Disease Models, Animal Epilepsy, Temporal Lobe - physiopathology Experimental and clinical factors Female Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Humans In vitro expansion Infarction, Middle Cerebral Artery - therapy Male Medical sciences Middle Aged Multipotent neural cells Multipotent Stem Cells - cytology Multipotent Stem Cells - transplantation Nervous system (semeiology, syndromes) Neural Stem Cells - cytology Neural Stem Cells - transplantation Neurology Primary Cell Culture - methods Random Allocation Rats Rats, Sprague-Dawley Stroke Temporal Lobe - cytology Temporal lobe epilepsy Therapeutic effects Young Adult |
title | Experimental and clinical factors influencing long-term stable in vitro expansion of multipotent neural cells from human adult temporal lobes |
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