RNA interference in vitro and in vivo using a novel chitosan/siRNA nanoparticle system.
Identifieur interne : 002243 ( PubMed/Curation ); précédent : 002242; suivant : 002244RNA interference in vitro and in vivo using a novel chitosan/siRNA nanoparticle system.
Auteurs : Kenneth A. Howard [Danemark] ; Ulrik L. Rahbek ; Xiudong Liu ; Christian K. Damgaard ; Sys Zoffmann Glud ; Morten Andersen ; Mads B. Hovgaard ; Alexander Schmitz ; Jens R. Nyengaard ; Flemming Besenbacher ; J Rgen KjemsSource :
- Molecular therapy : the journal of the American Society of Gene Therapy [ 1525-0016 ] ; 2006.
Descripteurs français
- KwdFr :
- Analyse spectrale, Animaux, Cellules cultivées, Chimie physique, Chitosane (), Gènes rapporteurs (génétique), Humains, Interférence par ARN, Microscopie à force atomique, Nanostructures (), Nanostructures (ultrastructure), Petit ARN interférent (), Petit ARN interférent (génétique), Phénomènes chimiques, Poumon (métabolisme), Souris.
- MESH :
English descriptors
- KwdEn :
- Animals, Cells, Cultured, Chemical Phenomena, Chemistry, Physical, Chitosan (chemistry), Genes, Reporter (genetics), Humans, Lung (metabolism), Mice, Microscopy, Atomic Force, Nanostructures (chemistry), Nanostructures (ultrastructure), RNA Interference, RNA, Small Interfering (chemistry), RNA, Small Interfering (genetics), Spectrum Analysis.
- MESH :
- chemical , chemistry : Chitosan, RNA, Small Interfering.
- chemistry : Nanostructures.
- genetics : Genes, Reporter, RNA, Small Interfering.
- metabolism : Lung.
- ultrastructure : Nanostructures.
- Animals, Cells, Cultured, Chemical Phenomena, Chemistry, Physical, Humans, Mice, Microscopy, Atomic Force, RNA Interference, Spectrum Analysis.
Abstract
This work introduces a novel chitosan-based siRNA nanoparticle delivery system for RNA interference in vitro and in vivo. The formation of interpolyelectrolyte complexes between siRNA duplexes (21-mers) and chitosan polymer into nanoparticles, ranging from 40 to 600 nm, was shown using atomic force microscopy and photon correlation spectroscopy. Rapid uptake (1 h) of Cy5-labeled nanoparticles into NIH 3T3 cells, followed by accumulation over a 24 h period, was visualized using fluorescence microscopy. Nanoparticle-mediated knockdown of endogenous enhanced green fluorescent protein (EGFP) was demonstrated in both H1299 human lung carcinoma cells and murine peritoneal macrophages (77.9% and 89.3% reduction in EGFP fluorescence, respectively). In addition, Western analysis showed approximately 90% reduced expression of BCR/ABL-1 leukemia fusion protein while BCR expression was unaffected in K562 (Ph(+)) cells after transfection using nanoparticles containing siRNA specific to the BCR/ABL-1 junction sequence. Effective in vivo RNA interference was achieved in bronchiole epithelial cells of transgenic EGFP mice after nasal administration of chitosan/siRNA formulations (37% and 43% reduction compared to mismatch and untreated control, respectively). These findings highlight the potential application of this novel chitosan-based system in RNA-mediated therapy of systemic and mucosal disease.
DOI: 10.1016/j.ymthe.2006.04.010
PubMed: 16829204
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<author><name sortKey="Liu, Xiudong" sort="Liu, Xiudong" uniqKey="Liu X" first="Xiudong" last="Liu">Xiudong Liu</name>
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<front><div type="abstract" xml:lang="en">This work introduces a novel chitosan-based siRNA nanoparticle delivery system for RNA interference in vitro and in vivo. The formation of interpolyelectrolyte complexes between siRNA duplexes (21-mers) and chitosan polymer into nanoparticles, ranging from 40 to 600 nm, was shown using atomic force microscopy and photon correlation spectroscopy. Rapid uptake (1 h) of Cy5-labeled nanoparticles into NIH 3T3 cells, followed by accumulation over a 24 h period, was visualized using fluorescence microscopy. Nanoparticle-mediated knockdown of endogenous enhanced green fluorescent protein (EGFP) was demonstrated in both H1299 human lung carcinoma cells and murine peritoneal macrophages (77.9% and 89.3% reduction in EGFP fluorescence, respectively). In addition, Western analysis showed approximately 90% reduced expression of BCR/ABL-1 leukemia fusion protein while BCR expression was unaffected in K562 (Ph(+)) cells after transfection using nanoparticles containing siRNA specific to the BCR/ABL-1 junction sequence. Effective in vivo RNA interference was achieved in bronchiole epithelial cells of transgenic EGFP mice after nasal administration of chitosan/siRNA formulations (37% and 43% reduction compared to mismatch and untreated control, respectively). These findings highlight the potential application of this novel chitosan-based system in RNA-mediated therapy of systemic and mucosal disease.</div>
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