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
Hauptverfasser: 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
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container_issue
container_start_page 168
container_title Experimental neurology
container_volume 240
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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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 (&gt;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 (&gt;40years) and a smaller sample volume (&lt;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><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. 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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 (&gt;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 (&gt;40years) and a smaller sample volume (&lt;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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