Olfactory ensheathing cells genetically modified to secrete GDNF to promote spinal cord repair

被引:129
作者
Cao, L
Liu, L
Chen, ZY
Wang, LM
Ye, JL
Qiu, HY
Lu, CL
He, C [1 ]
机构
[1] Second Mil Med Univ, Dept Neurobiol, Shanghai 200433, Peoples R China
[2] Qingdao Univ, Qingdao Med Coll, Dept Pathophysiol, Shandong 266021, Peoples R China
关键词
spinal cord injury; olfactory ensheathing cell; glial cell line-derived neurotrophic factor; transplantation; gene therapy;
D O I
10.1093/brain/awh072
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Olfactory ensheathing cell (OEC) transplantation has emerged as a very promising therapy for spinal cord repair. In this study, we tested the ability of genetically modified OECs to secrete high levels of glial cell line-derived neurotrophic factor (GDNF) to promote spinal cord repair. The GDNF gene was transduced into OECs using a retroviral-based system. The engineered OECs were first characterized by their ability to express and secrete biologically active GDNF in vitro. After implantation into the spinal cord of adult rats with complete spinal cord transection, OEC survival and GDNF production were examined. The locomotor functions of animals were assessed and axon regeneration was evaluated at the morphological level. To our knowledge, we report for the first time that the genetically modified OECs are capable of producing GDNF in vivo to significantly improve recovery after spinal cord injury (SCI). This work combined the outgrowth-promoting property of OECs with the neuroprotective effects of the additionally overexpressed neurotrophic factors SCI.
引用
收藏
页码:535 / 549
页数:15
相关论文
共 66 条
[1]   Identification of a human olfactory ensheathing cell that can effect transplant-mediated remyelination of demyelinated CNS axons [J].
Barnett, SC ;
Alexander, CL ;
Iwashita, Y ;
Gilson, JM ;
Crowther, J ;
Clark, L ;
Dunn, LT ;
Papanastassiou, V ;
Kennedy, PGE ;
Franklin, RJM .
BRAIN, 2000, 123 :1581-1588
[2]   Graded histological and locomotor outcomes after spinal cord contusion using the NYU weight-drop device versus transection [J].
Basso, DM ;
Beattie, MS ;
Bresnahan, JC .
EXPERIMENTAL NEUROLOGY, 1996, 139 (02) :244-256
[3]   MESENCEPHALIC DOPAMINERGIC-NEURONS PROTECTED BY GDNF FROM AXOTOMY-INDUCED DEGENERATION IN THE ADULT BRAIN [J].
BECK, KD ;
VALVERDE, J ;
ALEXI, T ;
POULSEN, K ;
MOFFAT, B ;
VANDLEN, RA ;
ROSENTHAL, A ;
HEFTI, F .
NATURE, 1995, 373 (6512) :339-341
[4]   GDNF gene delivery to injured adult CNS motor neurons promotes axonal growth, expression of the trophic neuropeptide CGRP, and cellular protection [J].
Blesch, A ;
Tuszynski, MH .
JOURNAL OF COMPARATIVE NEUROLOGY, 2001, 436 (04) :399-410
[5]  
Blits B, 2002, CELL TRANSPLANT, V11, P593
[6]   Adenoviral vector-mediated expression of a foreign gene in peripheral nerve tissue bridges implanted in the injured peripheral and central nervous system [J].
Blits, B ;
Dijkhuizen, PA ;
Carlstedt, TP ;
Poldervaart, H ;
Schiemanck, S ;
Boer, GJ ;
Verhaagen, J .
EXPERIMENTAL NEUROLOGY, 1999, 160 (01) :256-267
[7]   Intercostal nerve implants transduced with an adenoviral vector encoding neurotrophin-3 promote regrowth of injured rat corticospinal tract fibers and improve hindlimb function [J].
Blits, P ;
Dijkhuizen, PA ;
Boer, GJ ;
Verhaagen, J .
EXPERIMENTAL NEUROLOGY, 2000, 164 (01) :25-37
[8]  
Boruch AV, 2001, GLIA, V33, P225, DOI 10.1002/1098-1136(200103)33:3<225::AID-GLIA1021>3.0.CO
[9]  
2-Y
[10]   Neurotrophins are key mediators of the myelination program in the peripheral nervous system [J].
Chan, JR ;
Cosgaya, JM ;
Wu, YJ ;
Shooter, EM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (25) :14661-14668