Generation of dopaminergic neurons in the adult brain from mesencephalic precursor cells labeled with a nestin-GFP transgene

被引:164
作者
Sawamoto, K
Nakao, N
Kakishita, K
Ogawa, Y
Toyama, Y
Yamamoto, A
Yamaguchi, M
Mori, K
Goldman, SA
Itakura, T
Okano, H
机构
[1] Osaka Univ, Grad Sch Med, Biomed Res Ctr, Dept Neurosci,Div Neuroanat, Suita, Osaka 5650871, Japan
[2] Japanese Minist Educ Sci Sports Culture & Technol, Strateg Promot Syst Brain Sci, Chiyoda Ku, Tokyo 1008966, Japan
[3] Japan Sci & Technol Corp, Core Res Evolut Sci & Technol, Kawaguchi, Saitama 3320012, Japan
[4] Wakayama Med Coll, Dept Neurol Surg, Wakayama 6410012, Japan
[5] Keio Univ, Sch Med, Dept Orthopaed Surg, Shinjuku Ku, Tokyo 1608582, Japan
[6] Univ Tokyo, Grad Sch Med, Dept Physiol, Bunkyo Ku, Tokyo 1130033, Japan
[7] Cornell Univ, Med Ctr, Dept Neurol & Neurosci, New York, NY 10021 USA
[8] Keio Univ, Sch Med, Dept Physiol, Shinjuku Ku, Tokyo 1608582, Japan
关键词
Parkinson's disease; green fluorescent protein (GFP); fluorescence-activated cell sorting (FACS); dopaminergic neuron; precursor cells; transplantation;
D O I
10.1523/JNEUROSCI.21-11-03895.2001
中图分类号
Q189 [神经科学];
学科分类号
071006 [神经生物学];
摘要
Mesencephalic precursor cells may one day provide dopaminergic neurons for the treatment of Parkinson's disease. However, the generation of dopaminergic neurons from mesencephalic precursors has been difficult to follow, partly because an appropriate means for recognizing mesencephalic ventricular zone precursors has not been available. To visualize and isolate mesencephalic precursor cells from a mixed population, we used transgenic mice and rats carrying green fluorescent protein (GFP) cDNA under the control of the nestin enhancer. nestin-driven GFP was detected in the mesencephalic ventricular zone, and it colocalized with specific markers for neural precursor cells. In addition, data from flow-cytometry indicated that Prominin/CD133, a cell-surface marker for ventricular zone cells, was expressed specifically in these GFP-positive (GFP(+)) cells. After sorting by fluorescence-activated cell sorting, the GFP(+) cells proliferated in vitro and expressed precursor cell markers but not neuronal markers. Using clonogenic sphere formation assays, we showed that this sorted population was enriched in multipotent precursor cells that could differentiate into both neurons and glia. Importantly, many neurons generated from nestin-GFP-sorted mesencephalic precursors developed a dopaminergic phenotype in vitro. Finally, nestin-GFP(+) cells were transplanted into the striatum of a rat model of Parkinson's disease. Bromodeoxyuridine-tyrosine hydroxylase double-labeling revealed that the transplanted cells generated new dopaminergic neurons within the host striatum. The implanted cells were able to restore dopaminergic function in the host striatum, as assessed by a behavioral measure: recovery from amphetamine-induced rotation. Together, these findings indicate that precursor cells harvested from the embryonic ventral mesencephalon can generate dopaminergic neurons able to restore function to the chemically denervated adult striatum.
引用
收藏
页码:3895 / 3903
页数:9
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