Therapeutic benefit of TH-engineered mesenchymal stem cells for Parkinson's disease

被引:107
作者
Lu, LL [1 ]
Zhao, CL [1 ]
Liu, YJ [1 ]
Sun, XH [1 ]
Duan, CL [1 ]
Ji, M [1 ]
Zhao, HY [1 ]
Xu, QY [1 ]
Yang, H [1 ]
机构
[1] Capital Univ Med Sci, Beijing Ctr Neural Regenerat & Repairing, Beijing Inst Neurosci, Beijing 100054, Peoples R China
来源
BRAIN RESEARCH PROTOCOLS | 2005年 / 15卷 / 01期
关键词
mesenchymal stein cells; TH gene; Parkinson's disease; AAV; gene transfection;
D O I
10.1016/j.brainresprot.2005.03.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The present study was designed to assess the potential of marrow stromal cells (MSCs) to deliver therapeutic genes to the brain and result in biologically significant functional recovery. The tyrosine hydroxylase (TH) gene was transfected to MSCs with an adeno-associated virus (AAV) vector. MSCs expressing TH gene were transplanted into the striatum of Parkinson's disease (PD) rat. The asymmetric rotation of these models after apomorphine administration was detected every week after transplantation. Six weeks after grafting, animals were sacrificed. Some brains were sectioned to do TH immunohistochemistry. The others were used to detect the dopamine levels by high-performance liquid chromatograph and electrochemical detection (HPLC-ECD). The results showed that MSCs multiply rapidly and formed fibroblast colony-forming units in primary culture. The gene expression efficiency was about 75%. The rounds of asymmetric rotation after apomorphine administration decreased after TH-engineered MSCs were grafted. Histological examination showed that TH gene was expressed around the transplantation points. The dopamine level in the lesioned striatum of rats injected with TH-MSCs was significantly greater than that in rats treated with LacZ-MSCs (P < 0.05). All the data demonstrated that MSCs could readily be genetically engineered. Therefore, MSCs could be useful gene delivery vehicles of gene therapy for Parkinson's disease. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:46 / 51
页数:6
相关论文
共 28 条
[21]   Adult bone marrow stromal cells differentiate into neural cells in vitro [J].
Sanchez-Ramos, J ;
Song, S ;
Cardozo-Pelaez, F ;
Hazzi, C ;
Stedeford, T ;
Willing, A ;
Freeman, TB ;
Saporta, S ;
Janssen, W ;
Patel, N ;
Cooper, DR ;
Sanberg, PR .
EXPERIMENTAL NEUROLOGY, 2000, 164 (02) :247-256
[22]   SYNTHESIS OF L-3,4-DIHYDROXYPHENYLALANINE BY TYROSINE-HYDROXYLASE CDNA-TRANSFECTED C6 CELLS - APPLICATION FOR INTRACEREBRAL GRAFTING [J].
UCHIDA, K ;
TAKAMATSU, K ;
KANEDA, N ;
TOYA, S ;
TSUKADA, Y ;
KUROSAWA, Y ;
FUJITA, K ;
NAGATSU, T ;
KOHSAKA, S .
JOURNAL OF NEUROCHEMISTRY, 1989, 53 (03) :728-732
[23]   Contribution of transplanted bone marrow cells to Purkinje neurons in human adult brains [J].
Weimann, JM ;
Charlton, CA ;
Brazelton, TR ;
Hackman, RC ;
Blau, HM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (04) :2088-2093
[24]   Stable reprogrammed heterokaryons form spontaneously in Purkinje neurons after bone marrow transplant [J].
Weimann, JM ;
Johansson, CB ;
Trejo, A ;
Blau, HM .
NATURE CELL BIOLOGY, 2003, 5 (11) :959-966
[25]   GRAFTING FIBROBLASTS GENETICALLY MODIFIED TO PRODUCE L-DOPA IN A RAT MODEL OF PARKINSON DISEASE [J].
WOLFF, JA ;
FISHER, LJ ;
XU, L ;
JINNAH, HA ;
LANGLAIS, PJ ;
IUVONE, PM ;
OMALLEY, KL ;
ROSENBERG, MB ;
SHIMOHAMA, S ;
FRIEDMANN, T ;
GAGE, FH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :9011-9014
[26]  
Woodbury D, 2000, J NEUROSCI RES, V61, P364, DOI 10.1002/1097-4547(20000815)61:4<364::AID-JNR2>3.3.CO
[27]  
2-3
[28]   Human bone marrow stem cells exhibit neural phenotypes and ameliorate neurological deficits after grafting into the ischemic brain of rats [J].
Zhao, LR ;
Duan, WM ;
Reyes, M ;
Keene, CD ;
Verfaillie, CM ;
Low, WC .
EXPERIMENTAL NEUROLOGY, 2002, 174 (01) :11-20