Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.ymthe.2003.11.005
DC FieldValue
dc.titleNerve growth factor receptor-mediated gene transfer
dc.contributor.authorMa, N.
dc.contributor.authorWu, S.S.
dc.contributor.authorMa, Y.X.
dc.contributor.authorWang, X.
dc.contributor.authorZeng, J.
dc.contributor.authorTong, G.
dc.contributor.authorHuang, Y.
dc.contributor.authorWang, S.
dc.date.accessioned2014-10-27T08:34:31Z
dc.date.available2014-10-27T08:34:31Z
dc.date.issued2004-02
dc.identifier.citationMa, N., Wu, S.S., Ma, Y.X., Wang, X., Zeng, J., Tong, G., Huang, Y., Wang, S. (2004-02). Nerve growth factor receptor-mediated gene transfer. Molecular Therapy 9 (2) : 270-281. ScholarBank@NUS Repository. https://doi.org/10.1016/j.ymthe.2003.11.005
dc.identifier.issn15250016
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/101190
dc.description.abstractOne obstacle to effective gene therapies for neurological disorders lies in the cell-type diversity of the nervous system, making it difficult to direct gene delivery vectors to specific types of cells. To meet this challenge, we have developed a recombinant peptide-based gene delivery vector that targets nerve growth factor (NGF) receptors. The peptide comprises a cell-targeting domain derived from the NGF hairpin motif containing loops 1 and 2 linked to a DNA-binding domain composed of SPKR repeats. In PC12 cells, it activated the high-affinity NGF receptor, TrkA, and displayed NGF-like bioactivity by promoting neurite outgrowth and cell survival after serum deprivation. When combined with a low molecular weight of polyethylenimine (PEI), the peptide condensed plasmid DNA into nanoparticles that efficiently transferred exogenous genes into PC12 cells, enhancing reporter gene expression 5600-fold over peptide-free DNA/PEI complexes. Co-incubation with free NGF inhibited this effect. Furthermore, the peptide enhanced gene expression in NGF-receptor-rich rat primary cortex neurons but not glial cells. An in vivo experiment targeting TrkA-expressing dorsal root ganglia demonstrated that the peptide-containing complexes were 9- to 14-fold more efficient in transfection than controls. These properties make the chimeric peptide a promising gene delivery vector for targeting specific subtypes of neurons. Copyright © The American Society of Gene Therapy.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.ymthe.2003.11.005
dc.sourceScopus
dc.subjectDorsal root ganglia
dc.subjectGene delivery
dc.subjectNerve growth factor
dc.subjectNeurons
dc.subjectPC12 cells
dc.subjectReceptor
dc.typeArticle
dc.contributor.departmentBIOLOGICAL SCIENCES
dc.description.doi10.1016/j.ymthe.2003.11.005
dc.description.sourcetitleMolecular Therapy
dc.description.volume9
dc.description.issue2
dc.description.page270-281
dc.description.codenMTOHC
dc.identifier.isiut000188960900017
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.

Google ScholarTM

Check

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.