SiRNA delivery of ENAC mediated by targeted nanocomplex: a therapeutic strategy for cystic fibrosis

Manunta, Maria, Tagalakis, Aristides, Attwood, Martin, Aldossary, Ahmed M., Weng, Alexander, Barnes, Josephine L., Munye, Mustafa M., McAnulty, Robin, J. and Hart, Stephen L. (2017) SiRNA delivery of ENAC mediated by targeted nanocomplex: a therapeutic strategy for cystic fibrosis. Scientific Reports, 7. p. 700. ISSN 2045-2322 DOI https://doi.org/10.1038/s41598-017-00662-2

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Abstract

The inhibition of ENaC may have therapeutic potential in CF airways by reducing sodium hyperabsorption, restoring lung epithelial surface fluid levels, airway hydration and mucociliary function. The challenge has been to deliver siRNA to the lung with sufficient efficacy for a sustained therapeutic effect. We have developed a self-assembling nanocomplex formulation for siRNA delivery to the airways that consists of a liposome (DOTMA/DOPE; L), an epithelial targeting peptide (P) and siRNA (R). LPR formulations were assessed for their ability to silence expression of the transcript of the gene encoding the α-subunit of the sodium channel ENaC in cell lines and primary epithelial cells, in submerged cultures or grown in air-liquid interface conditions. LPRs, containing 50 nM or 100 nM siRNA, showed high levels of silencing, particularly in primary airway epithelial cells. When nebulised these nanocomplexes still retained their biophysical properties and transfection efficiencies. The silencing ability was determined at protein level by confocal microscopy and western blotting. In vivo data demonstrated that these nanoparticles had the ability to silence expression of the α-ENaC subunit gene. In conclusion, these findings show that LPRs can modulate the activity of ENaC and this approach might be promising as co-adjuvant therapy for cystic fibrosis.

Item Type: Article
Additional Information: his project was funded by a grant from the Wellcome Trust (WT094348MA) and supported by the National Institute for Health Research Biomedical Research Centre at Great Ormond Street Hospital for Children NHS Foundation Trust and University College London. M. Munye was supported by the Great Ormond Street Hospital Children’s Charity (GOSHCC) and the Child Health Research Appeal Trust (CHRAT), A.T. was supported by an EPSRC grant (EP/G061521/1) and A.W. was supported by the German Research Foundation (DFG).
Subjects: R Medicine > R Medicine (General)
R Medicine > RJ Pediatrics
Divisions: Biology
Date Deposited: 19 Apr 2018 08:45
URI: http://repository.edgehill.ac.uk/id/eprint/10244

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