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Enhanced lipoplex-mediated gene expression in mesenchymal stem cells using reiterated nuclear localization sequence peptides

  • University of Galway

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

40 Citations (Scopus)

Abstract

Background Mesenchymal stem cells (MSC) are widely regarded as a promising tool for cellular therapy applications, and genetic modification by safe, liposome-based vectors may enhance their therapeutic potential.Methods The present study describes the use of a cationic lipid vector (Lipofectamine 2000 (TM)) to deliver genes to MSC isolated from a number of species in vitro and determined the characteristics of this vector system in terms of dose, toxicity and the time course of expression. In addition, the optimal use of a nuclear localization sequence (NLS) to enhance gene expression was explored.Results Lipofection of human MSC did not adversely affect their ability to differentiate into osteogenic- and adipogenic lineages. Although human and rat MSC were found to take up lipoplexes with relative efficiency, lower levels of gene expression were detected in rabbit MSC, demonstrating a crucial effect of species. Peptides containing reiterated motifs of NLS were found to significantly improve on the level of transgene expression. Optimal gene delivery was observed when a three-fold reiterated NLS sequence was included in the liposome formulation.Conclusions Thus, nonviral gene delivery to MSC is feasible with efficiency being species dependent and can be enhanced by use of a three-fold reiterated NLS. Copyright (C) 2010 John Wiley Sons, Ltd.
Original languageEnglish (Ireland)
Pages (from-to)207-218
Number of pages12
JournalJOURNAL OF GENE MEDICINE
Volume12
Issue number2
DOIs
Publication statusPublished - 1 Feb 2010

Keywords

  • Enhanced gene delivery
  • Lipofection
  • Stem cells

Authors (Note for portal: view the doc link for the full list of authors)

  • Authors
  • Hoare, M,Greiser, U,Schu, S,Mashayekhi, K,Aydogan, E,Murphy, M,Barry, F,Ritter, T,O'Brien, T
  • Hoare, M;Greiser, U;Schu, S;Mashayekhi, K;Aydogan, E;Murphy, M;Barry, F;Ritter, T;O'Brien, T
  • Hoare M, Greiser U, Schu S, Mashayekhi K, Aydogan E, Murphy M, Barry F, Ritter T, O'Brien T

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