Remote adenoviral gene delivery to the spinal cord: Contralateral delivery and reinjection

被引:11
作者
Turner, DE
Noordmans, AI
Feldman, EL
Boulis, NM
机构
[1] Univ Michigan, Dept Neurol, Ann Arbor, MI USA
[2] Univ Michigan, Neurosurg Sect, Ann Arbor, MI USA
关键词
adenovirus; gene therapy; reinjection; sciatic nerve; spinal cord;
D O I
10.1097/00006123-200106000-00026
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
OBJECTIVE: This study characterizes the distribution of adenoviral genes in the spinal cord after viral vector injection into the sciatic nerve. It also evaluates the ability of repeated adenoviral sciatic nerve injections to prolong gene expression in the spinal cord. METHODS: Rat sciatic nerves were unilaterally coinjected with the retrograde tracer Fluoro-Cold (Fluorochrome, Inc., Denver, CO) and the adenoviral vector Ad5RSVntLacZ. The distribution of adenoviral gene expression in the spinal cord was compared with that of Fluoro-Cold. Next, levels of gene expression in the sciatic nerve and spinal cord were compared after single and repeated injections of Ad5RSVntLacZ. Finally, remote spinal cord gene expression in naive animals was compared with expression in animals that had been pretreated with subcutaneous Ad5RSVntLacZ inoculation. RESULTS: Viral gene expression was detected in all quadrants of the spinal cord gray matter, whereas Fluoro-Cold was detected only in the ipsilateral ventral horn (n = 5). This remote delivery was blocked by sciatic nerve transection (n = 10). Viral gene expression occurred in the sciatic nerve after both initial and repeated injections, whereas remote gene expression in the spinal cord was observed only after primary sciatic nerve injection (n = 24; P < 0.003). As with repeated sciatic nerve injections, subcutaneous inoculation with Ad5RSVntLacZ blocked subsequent remote spinal cord gene delivery (n = 8; P < 0.05). CONCLUSION: Remote viral gene delivery occurs in neurons without direct sciatic nerve projections but is dependent on intact peripheral nerves. Repeated injections fail to boost spinal cord gene expression, because of immune recognition of reinjected virus.
引用
收藏
页码:1309 / 1316
页数:8
相关论文
共 21 条
[1]   Adenoviral nerve growth factor and β-galactosidase transfer to spinal cord:: a behavioral and histological analysis [J].
Boulis, NM ;
Bhatia, V ;
Brindle, TI ;
Holman, HT ;
Krauss, DJ ;
Blaivas, M ;
Hoff, JT .
JOURNAL OF NEUROSURGERY, 1999, 90 (01) :99-108
[2]   Characterization of adenoviral gene expression in spinal cord after remote vector delivery [J].
Boulis, NM ;
Turner, DE ;
Dice, JA ;
Bhatia, V ;
Feldman, EL .
NEUROSURGERY, 1999, 45 (01) :131-137
[3]   Interactions between the immune system and gene therapy vectors: Bidirectional regulation of response and expression [J].
Bromberg, JS ;
Debruyne, LA ;
Qin, LH .
ADVANCES IN IMMUNOLOGY, VOL 69, 1998, 69 :353-409
[4]   ADENOVIRUS GENE-TRANSFER CAUSES INFLAMMATION IN THE BRAIN [J].
BYRNES, AP ;
RUSBY, JE ;
WOOD, MJA ;
CHARLTON, HM .
NEUROSCIENCE, 1995, 66 (04) :1015-1024
[5]   Adenoviral and adeno-associated viral transfer of genes to the peripheral nervous system [J].
Glatzel, W ;
Flechsig, E ;
Navarro, B ;
Klein, MA ;
Paterna, JC ;
Büeler, H ;
Aguzzi, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (01) :442-447
[6]   Transient immunosuppression with FK506 permits long-term expression of therapeutic genes introduced into the liver using recombinant adenoviruses in the rat [J].
Ilan, Y ;
Jona, VK ;
Sengupta, K ;
Davidson, A ;
Horwitz, MS ;
RoyChowdhury, N ;
RoyChowdhury, J .
HEPATOLOGY, 1997, 26 (04) :949-956
[7]   Modulation of cell-mediated immunity prolongs adenovirus-mediated transgene expression in sciatic nerve [J].
Jani, A ;
Menichella, D ;
Jiang, HY ;
Chbihi, T ;
Acsadi, G ;
Shy, ME ;
Kamholz, J .
HUMAN GENE THERAPY, 1999, 10 (05) :787-800
[8]   Humoral immune responses to adenovirus vectors in the brain [J].
Kajiwara, K ;
Byrnes, AP ;
Ohmoto, Y ;
Charlton, HM ;
Wood, MJA ;
Wood, KJ .
JOURNAL OF NEUROIMMUNOLOGY, 2000, 103 (01) :8-15
[9]   VIRUSES AS TRANSNEURONAL TRACERS [J].
KUYPERS, HGJM ;
UGOLINI, G .
TRENDS IN NEUROSCIENCES, 1990, 13 (02) :71-75
[10]   Application of recombinant adenovirus for in vivo gene delivery to spinal cord [J].
Liu, Y ;
Himes, BT ;
Moul, J ;
Huang, WL ;
Chow, SY ;
Tessler, A ;
Fischer, I .
BRAIN RESEARCH, 1997, 768 (1-2) :19-29