A Single Injection of Recombinant Adeno-Associated Virus into the Lumbar Cistern Delivers Transgene Expression Throughout the Whole Spinal Cord

被引:29
作者
Guo, Yansu [1 ,2 ]
Wang, Dan [3 ]
Qiao, Tao [2 ]
Yang, Chunxing [2 ]
Su, Qin [3 ,4 ]
Gao, Guangping [3 ,5 ]
Xu, Zuoshang [2 ,6 ,7 ]
机构
[1] Hebei Med Univ, Hosp 2, Dept Neurol, 215 Heping West Rd, Shijiazhuang 050000, Hebei, Peoples R China
[2] Univ Massachusetts, Dept Biochem & Mol Pharmacol, Med Sch Worcester, Worcester, MA 01605 USA
[3] Univ Massachusetts, Gene Therapy Ctr, Med Sch Worcester, Worcester, MA 01605 USA
[4] Univ Massachusetts, Viral Vector Core, Med Sch Worcester, Worcester, MA 01605 USA
[5] Univ Massachusetts, Med Sch Worcester, Microbiol & Physiol Syst, Worcester, MA 01605 USA
[6] Univ Massachusetts, Med Sch Worcester, Dept Cell Biol, Worcester, MA 01605 USA
[7] Univ Massachusetts, Med Sch Worcester, Neurosci Program, Worcester, MA 01605 USA
基金
美国国家卫生研究院;
关键词
rAAV; AAV; Amyotrophic lateral sclerosis; Pain; SMA; Gene therapy; CENTRAL-NERVOUS-SYSTEM; GENE DELIVERY; TRANSDUCTION; BRAIN; AAV9; TRANSPORT; NEURONS;
D O I
10.1007/s12035-015-9223-1
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The lack of methods to deliver transgene expression in spinal cord has hampered investigation of gene function and therapeutic targets for spinal cord diseases. Here, we report that a single intrathecal injection of recombinant adeno-associated virus rhesus-10 (rAAVrh10) into the lumbar cistern led to transgene expression in 60 to 90 % of the cells in the spinal cord. The transgene was expressed in all cell types, including neurons, glia, ependymal cells, and endothelial cells. Additionally, the transgene was expressed in some brain areas up to the frontal cortex and the olfactory bulb. The rAAV was distributed predominantly in the spinal cord, where its genome copy was over ten times that of the peripheral organs. Compared with intravenous injection, another method for rAAV delivery to the broad central nervous system (CNS), the intrathecal injection reduced the dosage of rAAV required to achieve similar or higher levels of transgene expression in the CNS by similar to 100-fold. Finally, the transduced areas were co-localized with the perivascular spaces of Virchow-Robin, from which the rAAV spreads further into the CNS parenchyma, thus suggesting that rAAV penetrated the CNS parenchyma through this pathway. Taken together, we have defined a fast and efficient method to deliver widespread transgene expression in mature spinal cord in mice. This method can be applied to stably overexpress or silence gene expression in the spinal cord to investigate gene functions in mammalian CNS. Additionally, this method can be applied to validate therapeutic targets for spinal cord diseases.
引用
收藏
页码:3235 / 3248
页数:14
相关论文
共 28 条
[11]  
Hordeaux J, 2015, GENE THER
[12]   A Paravascular Pathway Facilitates CSF Flow Through the Brain Parenchyma and the Clearance of Interstitial Solutes, Including Amyloid β [J].
Iliff, Jeffrey J. ;
Wang, Minghuan ;
Liao, Yonghong ;
Plogg, Benjamin A. ;
Peng, Weiguo ;
Gundersen, Georg A. ;
Benveniste, Helene ;
Vates, G. Edward ;
Deane, Rashid ;
Goldman, Steven A. ;
Nagelhus, Erlend A. ;
Nedergaard, Maiken .
SCIENCE TRANSLATIONAL MEDICINE, 2012, 4 (147)
[13]   Cerebrospinal fluid transport: a lymphatic perspective [J].
Johnston, M ;
Papaiconomou, C .
NEWS IN PHYSIOLOGICAL SCIENCES, 2002, 17 :227-230
[14]   Efficient neuronal gene transfer with AAV8 leads to neurotoxic levels of tau or green fluorescent proteins [J].
Klein, RL ;
Dayton, RD ;
Leidenheimer, NJ ;
Jansen, K ;
Golde, TE ;
Zweig, RM .
MOLECULAR THERAPY, 2006, 13 (03) :517-527
[15]   Viral vectors based on bidirectional cell-specific mammalian promoters and transcriptional amplification strategy for use in vitro and in vivo [J].
Liu, Beihui ;
Paton, Julian F. ;
Kasparov, Sergey .
BMC BIOTECHNOLOGY, 2008, 8 (1)
[16]   Intracellular transport of recombinant adeno-associated virus vectors [J].
Nonnenmacher, M. ;
Weber, T. .
GENE THERAPY, 2012, 19 (06) :649-658
[17]   The function and structure of the cerebrospinal fluid outflow system [J].
Pollay M. .
Cerebrospinal Fluid Research, 7 (1)
[18]   The Cre-loxP system: A versatile tool for targeting genes in a cell- and stage-specific manner [J].
Ray, MK ;
Fagan, SP ;
Brunicardi, FC .
CELL TRANSPLANTATION, 2000, 9 (06) :805-815
[19]  
Rennels M L, 1990, Adv Neurol, V52, P431
[20]   EVIDENCE FOR A PARAVASCULAR FLUID CIRCULATION IN THE MAMMALIAN CENTRAL NERVOUS-SYSTEM, PROVIDED BY THE RAPID DISTRIBUTION OF TRACER PROTEIN THROUGHOUT THE BRAIN FROM THE SUBARACHNOID SPACE [J].
RENNELS, ML ;
GREGORY, TF ;
BLAUMANIS, OR ;
FUJIMOTO, K ;
GRADY, PA .
BRAIN RESEARCH, 1985, 326 (01) :47-63