La maladie de Parkinson au Canada (serveur d'exploration)

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Survival, differentiation, and migration of bioreactor-expanded human neural precursor cells in a model of Parkinson disease in rats.

Identifieur interne : 002139 ( Main/Exploration ); précédent : 002138; suivant : 002140

Survival, differentiation, and migration of bioreactor-expanded human neural precursor cells in a model of Parkinson disease in rats.

Auteurs : Karim Mukhida [Canada] ; Behnam A. Baghbaderani ; Murray Hong ; Matthew Lewington ; Timothy Phillips ; Marcus Mcleod ; Arindom Sen ; Leo A. Behie ; Ivar Mendez

Source :

RBID : pubmed:18341411

English descriptors

Abstract

Fetal tissue transplantation for Parkinson disease (PD) has demonstrated promising results in experimental and clinical studies. However, the widespread clinical application of this therapeutic approach is limited by a lack of fetal tissue. Human neural precursor cells (HNPCs) are attractive candidates for transplantation because of their long-term proliferation activity. Furthermore, these cells can be reproducibly expanded in a standardized fashion in suspension bioreactors. In this study the authors sought to determine whether the survival, differentiation, and migration of HNPCs after transplantation depended on the region of precursor cell origin, intracerebral site of transplantation, and duration of their expansion.

DOI: 10.3171/FOC/2008/24/3-4/E7
PubMed: 18341411


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<term>Cell Differentiation (physiology)</term>
<term>Cell Movement (physiology)</term>
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<term>Fetus</term>
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<term>Parkinson Disease (etiology)</term>
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<term>Stem Cell Transplantation (methods)</term>
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<div type="abstract" xml:lang="en">Fetal tissue transplantation for Parkinson disease (PD) has demonstrated promising results in experimental and clinical studies. However, the widespread clinical application of this therapeutic approach is limited by a lack of fetal tissue. Human neural precursor cells (HNPCs) are attractive candidates for transplantation because of their long-term proliferation activity. Furthermore, these cells can be reproducibly expanded in a standardized fashion in suspension bioreactors. In this study the authors sought to determine whether the survival, differentiation, and migration of HNPCs after transplantation depended on the region of precursor cell origin, intracerebral site of transplantation, and duration of their expansion.</div>
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