Conversion of human umbilical cord mesenchymal stem cells in Wharton's jelly to dopaminergic neurons in vitro: Potential therapeutic application for parkinsonism

被引:340
作者
Fu, YS
Cheng, YC
Lin, MYA
Cheng, H
Chu, PM
Chou, SC
Shih, YH
Ko, MH
Sung, MS
机构
[1] Natl Yang Ming Univ, Sch Med, Dept Anat, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Sch Med, Inst Anat & Cell Biol, Taipei 112, Taiwan
[3] Natl Yang Ming Univ, Sch Med, Inst Physiol, Taipei 112, Taiwan
[4] Taipei Vet Gen Hosp, Dept Med Res & Educ, Taipei, Taiwan
[5] Taipei Vet Gen Hosp, Inst Neurol, Dept Neurosurg, Taipei, Taiwan
[6] Taipei Vet Gen Hosp, Inst Neurol, Neural Regenerat Lab, Taipei, Taiwan
[7] Taipei Vet Gen Hosp, Inst Neurol, Ctr Neural Regenerat, Taipei, Taiwan
[8] Taipei Med Univ, Sch Med, Taipei, Taiwan
[9] Natl Yang Ming Univ, Sch Med, Dept Pharmacol, Taipei 112, Taiwan
[10] China Med Univ, Inst Med Sci, Taichung, Taiwan
[11] China Med Univ, Dept Anat, Taichung, Taiwan
关键词
human umbilical mesenchymal stem cells; Parkinson's disease; transplantation; dopaminergic neuron; tyrosine hydroxylase;
D O I
10.1634/stemcells.2005-0053
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Human mesenchymal stem cells isolated from Wharton's Jelly of the umbilical cord were induced to transform into dopaminergic neurons in vitro through stepwise culturing in neuron-conditioned medium, sonic hedgehog, and FGF8. The success rate was 12.7%, as characterized by positive staining for tyrosine hydroxylase (TH), the rate-limiting catecholaminergic synthesizing enzyme, and dopamine being released into the culture medium. Transplantation of such cells into the striatum of rats previously made Parkinsonian by unilateral striatal lesioning with the dopaminergic neurotoxin 6-hydroxydopamine partially corrected the lesion-induced amphetamine-evoked rotation. Viability of the transplanted cells at least 4 months after transplantation was identified by positive TH staining and migration of 1.4 rum both rostrally and caudally. These results suggest that human umbilical mesenchymal stem cells have the potential for treatment of Parkinson's disease.
引用
收藏
页码:115 / 124
页数:10
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