Intracisternal delivery of AAV9 results in oligodendrocyte and Motor neuron transduction in the whole central nervous system of cats

被引:34
作者
Bucher, T. [1 ]
Dubreil, L. [2 ,3 ]
Colle, M-A [2 ,3 ]
Maquigneau, M. [1 ]
Deniaud, J. [2 ,3 ]
Ledevin, M. [2 ,3 ]
Moullier, P. [1 ,4 ]
Joussemet, B. [1 ]
机构
[1] Univ Nantes, Inst Rech Therapeut 1, INSERM, Lab Therapie Genique,UMR,U1089, F-44007 Nantes 01, France
[2] INRA, UMR, Anim Pathophysiol & Biotherapy Muscle & CNS Dis U, F-44026 Nantes, France
[3] LUNAM Univ, Nantes Atlantic Coll Vet Med Food Sci & Engn Onir, Nantes 03, France
[4] Univ Florida, Coll Med, Dept Mol Genet & Microbiol, Gainesville, FL USA
关键词
GENE-TRANSFER; SPINAL-CORD; NEUTRALIZING ANTIBODIES; DOMESTIC CATS; FELINE MODEL; VECTOR; BRAIN; SEROTYPE; IDENTIFICATION; EXPRESSION;
D O I
10.1038/gt.2014.16
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Systemic and intracerebrospinal fluid delivery of adeno-associated virus serotype 9 (AAV9) has been shown to achieve widespread gene delivery to the central nervous system (CNS). However, after systemic injection, the neurotropism of the vector has been reported to vary according to age at injection, with greater neuronal transduction in newborns and preferential glial cell tropism in adults. This difference has not yet been reported after cerebrospinal fluid (CSF) delivery. The present study analyzed both neuronal and glial cell transduction in the CNS of cats according to age of AAV9 CSF injection. In both newborns and young cats, administration of AAV9-GFP in the cisterna magna resulted in high levels of motor neurons (MNs) transduction from the cervical (84 +/- 5%) to the lumbar (99 +/- 1%) spinal cord, demonstrating that the remarkable tropism of AAV9 for MNs is not affected by age at CSF delivery. Surprisingly, numerous oligodendrocytes were also transduced in the brain and in the spinal cord white matter of young cats, but not of neonates, indicating that (i) age of CSF delivery influences the tropism of AAV9 for glial cells and (ii) AAV9 intracisternal delivery could be relevant for both the treatment of MN and demyelinating disorders.
引用
收藏
页码:522 / 528
页数:7
相关论文
共 40 条
[1]   High AAV vector purity results in serotype- and tissue-independent enhancement of transduction efficiency [J].
Ayuso, E. ;
Mingozzi, F. ;
Montane, J. ;
Leon, X. ;
Anguela, X. M. ;
Haurigot, V. ;
Edmonson, S. A. ;
Africa, L. ;
Zhou, S. ;
High, K. A. ;
Bosch, F. ;
Wright, J. F. .
GENE THERAPY, 2010, 17 (04) :503-510
[2]   Electrodiagnostic Testing and Histopathologic Changes Confirm Peripheral Nervous System Myelin Abnormalities in the Feline Model of Niemann-Pick Disease Type C [J].
Bagel, Jessica H. ;
Sikora, Tracey U. ;
Prociuk, Maria ;
Pesayco, Jill P. ;
Mizisin, Andrew P. ;
Shelton, G. Diane ;
Vite, Charles H. .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 2013, 72 (03) :256-262
[3]   Identification of the Galactose Binding Domain of the Adeno-Associated Virus Serotype 9 Capsid [J].
Bell, Christie L. ;
Gurda, Brittney L. ;
Van Vliet, Kim ;
Agbandje-McKenna, Mavis ;
Wilson, James M. .
JOURNAL OF VIROLOGY, 2012, 86 (13) :7326-7333
[4]   The AAV9 receptor and its modification to improve in vivo lung gene transfer in mice [J].
Bell, Christie L. ;
Vandenberghe, Luk H. ;
Bell, Peter ;
Limberis, Maria P. ;
Gao, Guang-Ping ;
Van Vliet, Kim ;
Agbandje-McKenna, Mavis ;
Wilson, James M. .
JOURNAL OF CLINICAL INVESTIGATION, 2011, 121 (06) :2427-2435
[5]   Systemic Gene Delivery in Large Species for Targeting Spinal Cord, Brain, and Peripheral Tissues for Pediatric Disorders [J].
Bevan, Adam K. ;
Duque, Sandra ;
Foust, Kevin D. ;
Morales, Pablo R. ;
Braun, Lyndsey ;
Schmelzer, Leah ;
Chan, Curtis M. ;
McCrate, Mary ;
Chicoine, Louis G. ;
Coley, Brian D. ;
Porensky, Paul N. ;
Kolb, Stephen J. ;
Mendell, Jerry R. ;
Burghes, Arthur H. M. ;
Kaspar, Brian K. .
MOLECULAR THERAPY, 2011, 19 (11) :1971-1980
[6]   Gene therapy for leukodystrophies [J].
Biffi, Alessandra ;
Aubourg, Patrick ;
Cartier, Nathalie .
HUMAN MOLECULAR GENETICS, 2011, 20 :R42-R53
[7]   Therapeutic Response in Feline Sandhoff Disease Despite Immunity to Intracranial Gene Therapy [J].
Bradbury, Allison M. ;
Cochran, J. Nicholas ;
McCurdy, Victoria J. ;
Johnson, Aime K. ;
Brunson, Brandon L. ;
Gray-Edwards, Heather ;
Leroy, Stanley G. ;
Hwang, Misako ;
Randle, Ashley N. ;
Jackson, Laura S. ;
Morrison, Nancy E. ;
Baek, Rena C. ;
Seyfried, Thomas N. ;
Cheng, Seng H. ;
Cox, Nancy R. ;
Baker, Henry J. ;
Cachon-Gonzalez, M. Begona ;
Cox, Timothy M. ;
Sena-Esteves, Miguel ;
Martin, Douglas R. .
MOLECULAR THERAPY, 2013, 21 (07) :1306-1315
[8]   scAAV9 Intracisternal Delivery Results in Efficient Gene Transfer to the Central Nervous System of a Feline Model of Motor Neuron Disease [J].
Bucher, Thomas ;
Colle, Marie-Anne ;
Wakeling, Erin ;
Dubreil, Laurence ;
Fyfe, John ;
Briot-Nivard, Delphine ;
Maquigneau, Maud ;
Raoul, Sylvie ;
Cherel, Yan ;
Astord, Stephanie ;
Duque, Sandra ;
Marais, Thibaut ;
Voit, Thomas ;
Moullier, Philippe ;
Barkats, Martine ;
Joussemet, Beatrice .
HUMAN GENE THERAPY, 2013, 24 (07) :670-682
[9]   Worldwide Epidemiology of Neutralizing Antibodies to Adeno-Associated Viruses [J].
Calcedo, Roberto ;
Vandenberghe, Luk H. ;
Gao, Guangping ;
Lin, Jianping ;
Wilson, James M. .
JOURNAL OF INFECTIOUS DISEASES, 2009, 199 (03) :381-390
[10]   Transduction characteristics of adeno-associated virus vectors expressing cap serotypes 7, 8, 9, and Rh10 in the mouse brain [J].
Cearley, CN ;
Wolfe, JH .
MOLECULAR THERAPY, 2006, 13 (03) :528-537