Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Brief Communication
  • Published:

Cationic lipids are essential for gene delivery mediated by intravenous administration of lipoplexes

Abstract

It was recently suggested that intravenously administered lipoplexes serve as a depot for the extracellular release of naked DNA and it is the naked DNA that mediates gene delivery in the lung. If this is the mechanism responsible for gene expression, we reasoned that continuous infusion of plasmid DNA should also result in significant lung expression in the absence of lipoplexes. Moreover, the infusion of non-coding plasmid DNA should inhibit gene delivery by lipoplexes. Infusion of plasmid DNA at a rate of 80 μg/min into the tail vein of a mouse resulted in a DNA serum concentration of 800 μg/ml. This was equivalent to a transcriptionally active DNA concentration of 120 μg/ml plasma as determined by an in vitro transfection assay. In spite of this high level of transcriptionally active DNA, there was no significant gene expression in the lung or any other organ tested. In addition, when lipoplex containing a reporter gene was injected, followed by an infusion of non-coding plasmid DNA as a potential competing molecule for DNA released from the lipoplex there was no effect on gene expression. These experiments indicate that the cationic lipid component of the lipoplex functions in an active capacity beyond that of a simple passive release matrix for plasmid DNA.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Figure 1
Figure 2
Figure 3
Figure 4

Similar content being viewed by others

References

  1. Felgner PL et al. Lipofection: a highly efficient, lipid-mediated DNA transfection procedure Proc Natl Acad Sci USA 1987 84: 7413–7417

    Article  CAS  Google Scholar 

  2. Felgner PL et al. Nomenclature for synthetic gene delivery systems (editorial) Hum Gene Ther 1997 8: 511–512

    Article  CAS  Google Scholar 

  3. Brigham KL et al. In vivo transfection of murine lungs with a functioning prokaryotic gene using a cationic liposome vehicle Am J Med Sci 1989 298: 278–281

    Article  CAS  Google Scholar 

  4. Caplen NJ et al. Liposome-mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis Nature Med 1995 1: 39–46

    Article  CAS  Google Scholar 

  5. Chadwick SL et al. Safety of a single aerosol administration of escalating doses of the cationic lipid GL-67/DOPE/DMPE-PEG5000 formulation to the lungs of normal volunteers Gene Therapy 1997 4: 937–942

    Article  CAS  Google Scholar 

  6. McLachlan G et al. Laboratory and clinical studies in support of cystic fibrosis gene therapy using pCMV-CFTR-DOTAP Gene Therapy 1996 3: 1113–1123

    CAS  PubMed  Google Scholar 

  7. Nabel GJ et al. Direct gene transfer with DNA-liposome complexes in melanoma: expression, biologic activity, and lack of toxicity in humans Proc Natl Acad Sci USA 1993 90: 11307–11311

    Article  CAS  Google Scholar 

  8. Nabel GJ et al. Immunotherapy for cancer by direct gene transfer into tumors Hum Gene Ther 1994 5: 57–77

    Article  CAS  Google Scholar 

  9. Stopeck AT et al. Phase I study of direct gene transfer of an allogeneic histocompatibility antigen, HLA-B7, in patients with metastatic melanoma J Clin Oncol 1997 15: 341–349

    Article  CAS  Google Scholar 

  10. Song YK, Liu F, Liu D . Enhanced gene expression in mouse lung by prolonging the retention time of intravenously injected plasmid DNA Gene Therapy 1998 5: 1531–1537

    Article  CAS  Google Scholar 

  11. Wolff JA et al. Direct gene transfer into mouse muscle in vivo Science 1990 247: 1465–1468

    Article  CAS  Google Scholar 

  12. Buttrick PM et al. Behavior of genes directly injected into the rat heart in vivo Circ Res 1992 70: 193–198

    Article  CAS  Google Scholar 

  13. Sikes ML, O’Malley BW Jr, Finegold MJ, Ledley FD . In vivo gene transfer into rabbit thyroid follicular cells by direct DNA injection Hum Gene Ther 1994 5: 837–844

    Article  CAS  Google Scholar 

  14. Hickman MA et al. Gene expression following direct injection of DNA into liver Hum Gene Ther 1994 5: 1477–1483

    Article  CAS  Google Scholar 

  15. Meyer KB et al. Intratracheal gene delivery to the mouse airway: characterization of plasmid DNA expression and pharmacokinetics Gene Therapy 1995 2: 450–460

    CAS  PubMed  Google Scholar 

  16. Yang JP, Huang L . Direct gene transfer to mouse melanoma by intratumor injection of free DNA Gene Therapy 1996 3: 542–548

    CAS  PubMed  Google Scholar 

  17. Nita I et al. Direct gene delivery to synovium. An evaluation of potential vectors in vitro and in vivo Arthritis Rheum 1996 39: 820–828

    Article  CAS  Google Scholar 

  18. Xu Y, Szoka FC Jr . Mechanism of DNA release from cationic liposome/DNA complexes used in cell transfection Biochemistry 1996 35: 5616–5623

    Article  CAS  Google Scholar 

  19. Barron LG, Meyer KB, Szoka FC Jr . Effects of complement depletion on the pharmacokinetics and gene delivery mediated by cationic lipid–DNA complexes Human Gene Ther 1998 9: 315–323

    Article  CAS  Google Scholar 

  20. Kawabata K, Takakura Y, Hashida M . The fate of plasmid DNA after intravenous injection in mice: involvement of scavenger receptors in its hepatic uptake Pharm Res 1995 12: 825–830

    Article  CAS  Google Scholar 

  21. Emlen W, Mannik M . Kinetics and mechanisms for removal of circulating single-stranded DNA in mice J Exp Med 1978 147: 684–699

    Article  CAS  Google Scholar 

  22. Tang MX, Redemann CT, Szoka FC Jr . In vitro gene delivery by degraded polyamidoamine dendrimers Bioconj Chem 1996 7: 703–714

    Article  CAS  Google Scholar 

  23. Legendre JY, Szoka FC Jr . Delivery of plasmid DNA into mammalian cell lines using pH-sensitive liposomes: comparison with cationic liposomes Pharm Res 1992 9: 1235–1242

    Article  CAS  Google Scholar 

  24. Sambrook J, Fritsch E, Maniatis T . Molecular Cloning: A Laboratory Manual Cold Spring Harbor Press, Cold Spring Harbor 1989

    Google Scholar 

Download references

Acknowledgements

This work was supported by the University of California Tobacco Related Disease Research Program 6RT-0109 and NIH DK46052. Dr Szoka has a financial interest in, and serves as a consultant to GeneMedicine Inc. a biotechnology company developing gene medicines.

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Barron, L., Uyechi, L. & Szoka, F. Cationic lipids are essential for gene delivery mediated by intravenous administration of lipoplexes. Gene Ther 6, 1179–1183 (1999). https://doi.org/10.1038/sj.gt.3300929

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/sj.gt.3300929

Keywords

This article is cited by

Search

Quick links