LPM Home
Contact LPM





JRGS Home
Aims and Scope
Current Issue
Forthcoming Articles
Archive
Editors




Information For Authors
General Information
Preparation of Manuscripts
How to Submit
Publication Charges
Review Process
Copyright Information

Print Information for Authors
(PDF)


Licence for Users
(PDF)


For Referees


For Librarians

Download
Manuscript Submission Form
.doc, .rtf, .pdf

   

Library Publishing Media

  CALL FOR PAPERS
Med J Ad

F
orthcoming
CONFERENCE and EXHIBITION
c
 
Journal of RNAi and Gene Silencing

 

Journal of RNAi and Gene Silencing (May 2008), 4(1), 281-288

Reseacrh Article

Tracking in vitro and in vivo siRNA electrotransfer in tumor cells

Aurelie Paganin-Gioannii †, Elisabeth Bellard†, Bettina Couderc‡, Justin Teissié †* and Muriel Golzio†*

ABSTRACT

RNA interference-mediated gene silencing offers the potential of targeted inhibition of disease-relevant genes. In vivo delivery of RNAi reagents can be obtained by a variety of approaches. Physical delivery methods appear safer and lack side effects. Electro-permeabilization is one of the non-viral methods successfully used to transfer small interfering RNAs (siRNAs) in vitro and in vivo. A promising approach may be, very little is known about the fundamental processes mediating siRNA transfer. In this study, we have investigated cellular delivery pathways involved in electro-delivery of siRNAs by a direct fluorescence imaging method. An Alexa-labeled siRNA was electro-transferred into murine melanoma cells stably-expressing the enhanced green fluorescent protein (eGFP) target reporter gene. The silencing of eGFP gene expression was quantified by time-lapsed fluorescence microscopy. Fluorescently-labeled siRNAs were found distributed homogeneously in cytoplasm 48 hours after electro-transfer, apparently by diffusion. Furthermore, siRNAs showed homogeneous distribution in vivo 48 hrs after intra-tumoral injection followed by electro- permeabilization. Histological fluorescence microscopy showed that siRNAs were mostly localized in the cytoplasm. Overall, this study shows that electro-permeabilization facilitates cytoplasmic distribution of siRNA, both in cultured cells and in vivo. This method offers a potential therapeutic tool to facilitate direct siRNA penetration into solid tumors.

KEYWORDS: Electro-permeabilization, electro-poration, RNAi, tumors, fluorescence microscopy

† IPBS CNRS (UMR 5089 Université de Toulouse III, CNRS), 205 Route de Narbonne, 31077 Toulouse France

‡ Université de Toulouse III ; Institut C. Regaud, 20-24 rue du Pont ST Pierre, 31052 Toulouse France.

*Correspondence to: Muriel Golzio and Justin Teissié, Email: muriel.golzio@ipbs.fr (MG) or justin.teissie@ipbs.fr (JT), Tel: +33 561 175812/13; Fax: +33 561 175994

© Copyright The Authors

( Received 29 April 2008; Revised 15 May 2008; Accepted 20 May 2008)

Privacy | Disclaimer

©Library Publishing Media. All rights reserved.