Literature DB >> 22034030

Recombinant AAV delivery to the central nervous system.

Olivier Bockstael1, Kevin D Foust, Brian Kaspar, Liliane Tenenbaum.   

Abstract

Recombinant AAV-mediated gene delivery to the CNS can be performed either by direct delivery at the target site or from the periphery, using intramuscular injections and retrograde transport along motor neuron projections or intravenous injections and blood-brain barrier crossing.In this chapter, we describe: 1. Methods for recombinant virus administration, including stereotactic surgery, intramuscular, and intravenous administration. 2. Methods to evaluate the number and biodistribution of brain and spinal cord cells expressing the transgene by immunohistochemisty as well as the amount of transgene product by ELISA in the target region. 3. Methods to characterize the cellular specificity of transgene expression by double immunofluorescence. 4. Methods to quantify the amounts of viral DNA as well as of transgene mRNA by quantitative PCR and RT-PCR, respectively.

Mesh:

Year:  2011        PMID: 22034030     DOI: 10.1007/978-1-61779-370-7_7

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  7 in total

1.  Transduction of the central nervous system after intracerebroventricular injection of adeno-associated viral vectors in neonatal and juvenile mice.

Authors:  Shervin Gholizadeh; Sujeenthar Tharmalingam; Margarita E Macaldaz; David R Hampson
Journal:  Hum Gene Ther Methods       Date:  2013-08-03       Impact factor: 2.396

2.  Rapid transgene expression in multiple precursor cell types of adult rat subventricular zone mediated by adeno-associated type 1 vectors.

Authors:  Olivier Bockstael; Catherine Melas; Catherine Pythoud; Marc Levivier; Douglas McCarty; R Jude Samulski; Olivier De Witte; Liliane Tenenbaum
Journal:  Hum Gene Ther       Date:  2012-06-05       Impact factor: 5.695

3.  Correcting Neuromuscular Deficits With Gene Therapy in Pompe Disease.

Authors:  Adrian G Todd; Jessica A McElroy; Robert W Grange; David D Fuller; Glenn A Walter; Barry J Byrne; Darin J Falk
Journal:  Ann Neurol       Date:  2015-06-30       Impact factor: 10.422

4.  Potential role of recombinant adeno-associated virus human thioredoxin-PR39 in cell and vascular protection against hypoxia.

Authors:  Xi-Yun Ruan; Ying-Chun Liang; Bin DU; You-Ting Lin; Yu-Dong Guo; Jing Zhao; Shan Li; Ji-Feng Li; Qin-Jian Sun; Yi-Feng DU
Journal:  Exp Ther Med       Date:  2015-02-17       Impact factor: 2.447

5.  Comparative impact of AAV and enzyme replacement therapy on respiratory and cardiac function in adult Pompe mice.

Authors:  Darin J Falk; Meghan S Soustek; Adrian Gary Todd; Cathryn S Mah; Denise A Cloutier; Jeffry S Kelley; Nathalie Clement; David D Fuller; Barry J Byrne
Journal:  Mol Ther Methods Clin Dev       Date:  2015-03-25       Impact factor: 6.698

6.  Single AAV-Mediated CRISPR-SaCas9 Inhibits HSV-1 Replication by Editing ICP4 in Trigeminal Ganglion Neurons.

Authors:  Yuxi Chen; Shengyao Zhi; Puping Liang; Qi Zheng; Mengni Liu; Qi Zhao; Jian Ren; Jun Cui; Junjiu Huang; Yizhi Liu; Zhou Songyang
Journal:  Mol Ther Methods Clin Dev       Date:  2020-05-22       Impact factor: 6.698

7.  Expression of Fused in sarcoma mutations in mice recapitulates the neuropathology of FUS proteinopathies and provides insight into disease pathogenesis.

Authors:  Christophe Verbeeck; Qiudong Deng; Mariely Dejesus-Hernandez; Georgia Taylor; Carolina Ceballos-Diaz; Jannet Kocerha; Todd Golde; Pritam Das; Rosa Rademakers; Dennis W Dickson; Thomas Kukar
Journal:  Mol Neurodegener       Date:  2012-10-10       Impact factor: 14.195

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.