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Neural stem cells: properties and therapeutic potentials for hypoxic-ischemic brain injury in newborn infants

Authors
 Il-Shin Lee  ;  Kwangsoo Jung  ;  Miri Kim  ;  Kook In Park 
Citation
 PEDIATRICS INTERNATIONAL, Vol.52(6) : 855-865, 2010 
Journal Title
 PEDIATRICS INTERNATIONAL 
ISSN
 1328-8067 
Issue Date
2010
MeSH
Animals ; Brain/physiopathology ; Cell Differentiation/physiology ; Cell Movement/physiology ; Disease Models, Animal ; Embryonic Stem Cells/cytology ; Embryonic Stem Cells/transplantation ; Genetic Therapy/methods ; Humans ; Hypoxia-Ischemia, Brain/physiopathology ; Hypoxia-Ischemia, Brain/surgery* ; Infant, Newborn ; Neural Stem Cells/cytology ; Neural Stem Cells/transplantation* ; Neurogenesis/physiology ; Tissue Engineering/methods
Abstract
Neural stem cells (NSCs) are defined by their ability to self-renew, to differentiate into cells of all glial and neuronal lineages throughout the neuraxis, and to populate developing or degenerating central nervous system (CNS) regions. The recognition that NSCs propagated in culture could be reimplanted into the mammalian brain, where they might integrate appropriately throughout the mammalian CNS and stably express foreign genes, has unveiled a new role for neural transplantation and gene therapy and a possible strategy for addressing the CNS manifestations of diseases that hitherto had been refractory to intervention. An intriguing phenomenon with possible therapeutic potentials has begun to emerge from our observations of the behavior of NSCs in animal models of neonatal hypoxic-ischemic (HI) brain injury. During phases of active neurodegeneration, factors seem to be transiently elaborated to which NSCs may respond by migrating to degenerating regions and differentiating specifically towards replacement of dying neural cells. NSCs may attempt to repopulate and reconstitute ablated regions. These 'repair mechanisms' may actually reflect the reexpression of basic developmental principles that may be harnessed for therapeutic ends. In addition, NSCs may serve as vehicles for gene delivery and appear capable of simultaneous neural cell replacement and gene therapy (e.g. with factors that might enhance neuronal differentiation, neurites outgrowth, proper connectivity, and/or neuroprotection). When combined with certain synthetic biomaterials, NSCs may be even more effective in 'engineering' the damaged CNS towards reconstitution. We have also cultured human NSCs or progenitors as neurospheres which were derived from fetal cadavers at 13 weeks of gestation, and transplanted them into HI-injured immature brains to investigate their therapeutic potentials in this type of model.
Full Text
http://onlinelibrary.wiley.com/doi/10.1111/j.1442-200X.2010.03266.x/abstract
DOI
10.1111/j.1442-200X.2010.03266.x
Appears in Collections:
1. College of Medicine (의과대학) > Yonsei Biomedical Research Center (연세의생명연구원) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Pediatrics (소아청소년과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Mi Ri(김미리) ORCID logo https://orcid.org/0000-0002-0380-1677
Park, Kook In(박국인) ORCID logo https://orcid.org/0000-0001-8499-9293
Lee, Il Shin(이일신)
Jung, Kwang Soo(정광수) ORCID logo https://orcid.org/0000-0001-7365-7247
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/102616
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