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Developmental cues and persistent neurogenic potential within an in vitro neural niche

BACKGROUND: Neurogenesis, the production of neural cell-types from neural stem cells (NSCs), occurs during development as well as within select regions of the adult brain. NSCs in the adult subependymal zone (SEZ) exist in a well-categorized niche microenvironment established by surrounding cells an...

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Autores principales: Pierret, Chris, Morrison, Jason A, Rath, Prakash, Zigler, Rachel E, Engel, Laura A, Fairchild, Corinne L, Shi, Huidong, Maruniak, Joel A, Kirk, Mark D
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2824744/
https://www.ncbi.nlm.nih.gov/pubmed/20074373
http://dx.doi.org/10.1186/1471-213X-10-5
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author Pierret, Chris
Morrison, Jason A
Rath, Prakash
Zigler, Rachel E
Engel, Laura A
Fairchild, Corinne L
Shi, Huidong
Maruniak, Joel A
Kirk, Mark D
author_facet Pierret, Chris
Morrison, Jason A
Rath, Prakash
Zigler, Rachel E
Engel, Laura A
Fairchild, Corinne L
Shi, Huidong
Maruniak, Joel A
Kirk, Mark D
author_sort Pierret, Chris
collection PubMed
description BACKGROUND: Neurogenesis, the production of neural cell-types from neural stem cells (NSCs), occurs during development as well as within select regions of the adult brain. NSCs in the adult subependymal zone (SEZ) exist in a well-categorized niche microenvironment established by surrounding cells and their molecular products. The components of this niche maintain the NSCs and their definitive properties, including the ability to self-renew and multipotency (neuronal and glial differentiation). RESULTS: We describe a model in vitro NSC niche, derived from embryonic stem cells, that produces many of the cells and products of the developing subventricular zone (SVZ) and adult SEZ NSC niche. We demonstrate a possible role for apoptosis and for components of the extracellular matrix in the maintenance of the NSC population within our niche cultures. We characterize expression of genes relevant to NSC self-renewal and the process of neurogenesis and compare these findings to gene expression produced by an established neural-induction protocol employing retinoic acid. CONCLUSIONS: The in vitro NSC niche shows an identity that is distinct from the neurally induced embryonic cells that were used to derive it. Molecular and cellular components found in our in vitro NSC niche include NSCs, neural progeny, and ECM components and their receptors. Establishment of the in vitro NSC niche occurs in conjunction with apoptosis. Applications of this culture system range from studies of signaling events fundamental to niche formation and maintenance as well as development of unique NSC transplant platforms to treat disease or injury.
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spelling pubmed-28247442010-02-20 Developmental cues and persistent neurogenic potential within an in vitro neural niche Pierret, Chris Morrison, Jason A Rath, Prakash Zigler, Rachel E Engel, Laura A Fairchild, Corinne L Shi, Huidong Maruniak, Joel A Kirk, Mark D BMC Dev Biol Research article BACKGROUND: Neurogenesis, the production of neural cell-types from neural stem cells (NSCs), occurs during development as well as within select regions of the adult brain. NSCs in the adult subependymal zone (SEZ) exist in a well-categorized niche microenvironment established by surrounding cells and their molecular products. The components of this niche maintain the NSCs and their definitive properties, including the ability to self-renew and multipotency (neuronal and glial differentiation). RESULTS: We describe a model in vitro NSC niche, derived from embryonic stem cells, that produces many of the cells and products of the developing subventricular zone (SVZ) and adult SEZ NSC niche. We demonstrate a possible role for apoptosis and for components of the extracellular matrix in the maintenance of the NSC population within our niche cultures. We characterize expression of genes relevant to NSC self-renewal and the process of neurogenesis and compare these findings to gene expression produced by an established neural-induction protocol employing retinoic acid. CONCLUSIONS: The in vitro NSC niche shows an identity that is distinct from the neurally induced embryonic cells that were used to derive it. Molecular and cellular components found in our in vitro NSC niche include NSCs, neural progeny, and ECM components and their receptors. Establishment of the in vitro NSC niche occurs in conjunction with apoptosis. Applications of this culture system range from studies of signaling events fundamental to niche formation and maintenance as well as development of unique NSC transplant platforms to treat disease or injury. BioMed Central 2010-01-14 /pmc/articles/PMC2824744/ /pubmed/20074373 http://dx.doi.org/10.1186/1471-213X-10-5 Text en Copyright ©2010 Pierret et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Pierret, Chris
Morrison, Jason A
Rath, Prakash
Zigler, Rachel E
Engel, Laura A
Fairchild, Corinne L
Shi, Huidong
Maruniak, Joel A
Kirk, Mark D
Developmental cues and persistent neurogenic potential within an in vitro neural niche
title Developmental cues and persistent neurogenic potential within an in vitro neural niche
title_full Developmental cues and persistent neurogenic potential within an in vitro neural niche
title_fullStr Developmental cues and persistent neurogenic potential within an in vitro neural niche
title_full_unstemmed Developmental cues and persistent neurogenic potential within an in vitro neural niche
title_short Developmental cues and persistent neurogenic potential within an in vitro neural niche
title_sort developmental cues and persistent neurogenic potential within an in vitro neural niche
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2824744/
https://www.ncbi.nlm.nih.gov/pubmed/20074373
http://dx.doi.org/10.1186/1471-213X-10-5
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