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Multipotent Neural Stem Cells from the Adult Tegmentum with Dopaminergic Potential Develop Essential Properties of FunctionalNeurons

Authors
 Andreas Hermann  ;  Martina Maisel  ;  Florian Wegner  ;  Stefan Liebau  ;  Dong-Wook Kim  ;  Manfred Gerlach  ;  Johannes Schwarz  ;  Kwang-Soo Kim  ;  Alexander Storch 
Citation
 STEM CELLS, Vol.24(4) : 949-964, 2006 
Journal Title
 STEM CELLS 
ISSN
 1066-5099 
Issue Date
2006
MeSH
Animals ; Base Sequence ; Biomarkers ; Cell Cycle ; Cell Differentiation ; Cell Proliferation ; Clone Cells ; Dopamine/metabolism* ; In Vitro Techniques ; Male ; Mice ; Mice, Inbred C57BL ; Multipotent Stem Cells/cytology* ; Multipotent Stem Cells/metabolism* ; Neurons/cytology* ; Neurons/metabolism* ; RNA/genetics ; RNA/metabolism ; Serotonin/metabolism ; Tegmentum Mesencephali/cytology* ; Tegmentum Mesencephali/metabolism* ; gamma-Aminobutyric Acid/metabolism
Keywords
Adult neurogenesis ; Neural stem cells ; Dopaminergic differentiation ; Parkinson's disease ; Electrophysiology ; Neuroregeneration
Abstract
Neurogenesis in the adult brain occurs within the two principal neurogenic regions: the hippocampus and the subventricular zone of the lateral ventricles. The occurrence of adult neurogenesis in non-neurogenic regions, including the midbrain, remains controversial, but isolation of neural stem cells (NSCs) from several parts of the adult brain, including the substantia nigra, has been reported. Nevertheless, it is unclear whether adult NSCs do have the capacity to produce functional dopaminergic neurons, the cell type lost in Parkinson's disease. Here, we describe the isolation, expansion, and in vitro characterization of adult mouse tegmental NSCs (tNSCs) and their differentiation into functional nerve cells, including dopaminergic neurons. These tNSCs showed neurosphere formation and expressed high levels of early neuroectodermal markers, such as the proneural genes NeuroD1, Neurog2, and Olig2, the NSC markers Nestin and Musashi1, and the proliferation markers Ki67 and BrdU (5-bromo-2-deoxyuridine). The cells showed typical propidium iodide–fluorescence-activated cell sorting analysis of slowly dividing cells. In the presence of selected growth factors, tNSCs differentiated into astroglia, oligodendroglia, and neurons expressing markers for cholinergic, GABAergic, and glutamatergic cells. Electrophysiological analyses revealed functional properties of mature nerve cells, such as tetrodotoxin-sensitive sodium channels, action potentials, as well as currents induced by GABA (γ-aminobutyric acid), glutamate, and NMDA (N-methyl-d-aspartate). Clonal analysis demonstrated that individual NSCs retain the capacity to generate both glia and neurons. After a multistep differentiation protocol using co-culture conditions with PA6 stromal cells, a small number of cells acquired morphological and functional properties of dopaminergic neurons in culture. Here, we demonstrate the existence of adult tNSCs with functional neurogenic and dopaminergic potential, a prerequisite for future endogenous cell replacement strategies in Parkinson's disease.
Files in This Item:
T200600144.pdf Download
DOI
10.1634/stemcells.2005-0192
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Physiology (생리학교실) > 1. Journal Papers
Yonsei Authors
Kim, Dong Wook(김동욱) ORCID logo https://orcid.org/0000-0002-5025-1532
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/108926
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