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The extra- and intracellular barriers to lipid and adenovirus-mediated pulmonary gene transfer in native sheep airway epithelium

Abstract

Gene transfer to the respiratory epithelium is currently suboptimal and may be helped by the identification of limiting biological barriers. We have, therefore, developed an ex vivo model which retains many of the characteristics of in vivo native airways including mucociliary clearance, mucus coverage and an intact cellular structure. Using this model we have demonstrated several barriers to gene transfer. Liposome-mediated gene transfer was inhibited by normal mucus, with removal of this layer increasing expression approximately 25-fold. In addition both liposome and adenovirus were inhibited by CF sputum. The apical membrane represented a significant barrier to both agents. Adenovirus-mediated expression could be significantly augmented by increasing contact time or by pretreatment of tissues with a nominally calcium-free medium. The presence of these extracellular and plasma membrane barriers appeared to be the key parameters responsible for the approximately three log difference in gene expression found in vitro compared with our ex vivo model. Cytoskeletal elements and the cell cycle also influenced in vitro gene transfer, and represent further barriers which need to be overcome.

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References

  1. 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  PubMed  Google Scholar 

  2. Porteous DJ et al. Evidence for safety and efficacy of DOTAP cationic liposome mediated CFTR gene transfer to the nasal epithelium of patients with cystic fibrosis Gene Therapy 1997 4: 210–218

    Article  CAS  PubMed  Google Scholar 

  3. Gill DR et al. A placebo-controlled study of liposome-mediated gene transfer to the nasal epithelium of patients with cystic fibrosis Gene Therapy 1997 4: 199–209

    Article  CAS  PubMed  Google Scholar 

  4. Zabner J et al. Adenovirus-mediated gene transfer transiently corrects the chloride transport defect in nasal epithelia of patients with cystic fibrosis Cell 1993 75: 207–216

    Article  CAS  PubMed  Google Scholar 

  5. Crystal RG et al. Administration of an adenovirus containing the human CFTR cDNA to the respiratory tract of individuals with cystic fibrosis Nat Genet 1994 8: 42–51

    Article  CAS  PubMed  Google Scholar 

  6. Knowles MR et al. A controlled study of adenovirus-vector-mediated gene transfer in the nasal epithelium of patients with cystic fibrosis New Engl J Med 1995 333: 823–831

    Article  CAS  PubMed  Google Scholar 

  7. Bellon G et al. Aerosol administration of a recombinant adenovirus expressing CFTR to cystic fibrosis patients: A phase I clinical trial Hum Gene Ther 1997 4: 15–25

    Article  Google Scholar 

  8. Zabner J et al. Repeat administration of an adenovirus vector encoding cystic fibrosis transmembrane conductance regulator to the nasal epithelium of patients with cystic fibrosis J Clin Invest 1996 97: 1504–1511

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Dorin JR et al. A demonstration using mouse models that successful gene therapy for cystic fibrosis requires only partial gene correction Gene Therapy 1996 3: 797–801

    CAS  PubMed  Google Scholar 

  10. Johnson LG et al. Efficiency of gene transfer for restoration of normal airway epithelial function in cystic fibrosis Nat Genet 1992 2: 21–25

    Article  CAS  PubMed  Google Scholar 

  11. Matsui H, Johnson LG, Randell SH, Boucher RC . Loss of binding and entry of liposome-DNA complexes decreases transfection efficiency in differentiated airway epithelial cells J Biol Chem 1997 272: 1117–1126

    Article  CAS  PubMed  Google Scholar 

  12. Zabner J et al. Cellular and molecular barriers to gene transfer by a cationic lipid J Biol Chem 1995 270: 18997–19007

    Article  CAS  PubMed  Google Scholar 

  13. Lee ER et al. Detailed analysis of structures and formulations of cationic lipids for efficient gene transfer to the lung Hum Gene Ther 1996 7: 1701–1717

    Article  CAS  PubMed  Google Scholar 

  14. Grubb BR et al. Inefficient gene transfer by adenovirus vector to cystic fibrosis airway epithelia of mice and humans Nature 1994 371: 802–806

    Article  CAS  PubMed  Google Scholar 

  15. Zabner J et al. Lack of high affinity fiber receptor activity explains the resistance of ciliated airway epithelia to adenovirus infection J Clin Invest 1997 100: 1144–1149

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  16. Pilewski JM et al. Adenonovirus-mediated gene transfer to human bronchial submucosal glands using xenografts Am J Physiol 1995 268: L657–L665

    CAS  PubMed  Google Scholar 

  17. Worgall S, Wolff G, Falck-Pederson E, Crystal RG . Innate immune mechanisms dominate elimination of adenoviral vectors following in vivo administration Hum Gene Ther 1997 8: 37–44

    Article  CAS  PubMed  Google Scholar 

  18. Mack CA et al. Circumvention of anti-adenovirus neutralising immunity by administration of an adenoviral vector of an alternate serotype Hum Gene Ther 1997 8: 99–109

    Article  CAS  PubMed  Google Scholar 

  19. Scaria A et al. Antibody to CD40 ligand inhibits both humoral and cellular immune responses to adenoviral vectors and facilitates repeated administration to mouse airway Gene Therapy 1997 4: 611–617

    Article  CAS  PubMed  Google Scholar 

  20. Yang Y et al. Inactivation of E2a in recombinant adenoviruses improves the prospect for gene therapy in cystic fibrosis Nat Genet 1994 7: 362–369

    Article  CAS  PubMed  Google Scholar 

  21. Zabner J et al. Safety and efficacy of repetitive adenovirus-mediated transfer of CFTR cDNA to airway epithelia of primates and cotton rats Nat Genet 1994 6: 75–83

    Article  CAS  PubMed  Google Scholar 

  22. Brody SL et al. Acute responses of non-human primates to airway delivery of an adenovirus vector containing the human cystic fibrosis transmembrane conductance regulator cDNA Hum Gene Ther 1994 5: 821–836

    Article  CAS  PubMed  Google Scholar 

  23. Dupuit F et al. Regenerating cells in human airway surface epithelium represent preferential targets for recombinant adenovirus Hum Gene Ther 1995 6: 1185–1193

    Article  CAS  PubMed  Google Scholar 

  24. Fasbender A, Zabner J, Zeiher BG, Welsh MJ . A low rate of cell proliferation and reduced DNA uptake limit cationic lipid-mediated gene transfer to primary cultures of ciliated human airway epithelia Gene Therapy 1997 4: 1173–1180

    Article  CAS  PubMed  Google Scholar 

  25. Wills PJ et al. The ciliary transportability of sputum is slow on the mucus-depleted bovine trachea Am J Respir Crit Care Med 1995 151: 1255–1258

    CAS  PubMed  Google Scholar 

  26. Stern M et al. The effect of mucolytic agents on gene transfer across a CF sputum barrierin vitro Gene Therapy 1998 5: 91–98

    Article  CAS  PubMed  Google Scholar 

  27. Bhat M et al. Regulation of tight junction permeability by calcium mediators and cell cytoskeleton in rabbit tracheal epithelium Pharm Res 1993 10: 991–997

    Article  CAS  PubMed  Google Scholar 

  28. Sheils CA et al. Actin filaments mediate DNA fiber formation in chronic inflammatory airway disease Am J Pathol 1996 148: 919–927

    CAS  PubMed  PubMed Central  Google Scholar 

  29. Fasbender A et al. Complexes of adenovirus with polycationic polymers and cationic lipids increase the efficiency of gene transfer in vitro and in vivo J Biol Chem 1997 272: 6479–6489

    Article  CAS  PubMed  Google Scholar 

  30. Arcasoy SM et al. Polycations increase the efficiency of adenovirus-mediated gene transfer to epithelial and endothelial cells in vitro Gene Therapy 1997 4: 32–38

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  31. Girod S et al. Role of physiochemical properties of mucus in the protection of the respiratory epitheium Eur Respir J 1992 5: 477–487

    CAS  PubMed  Google Scholar 

  32. Lopez-Vidriero MT . Mucus as a natural barrier Respiration 1989 55: 28–32

    Article  PubMed  Google Scholar 

  33. Albanese CT et al. Role of intestinal mucus in transepithelial passage of bacteria across the intact ileum in vitro Surgery 1994 116: 76–82

    CAS  PubMed  Google Scholar 

  34. Sandberg JW et al. Improving access to intestinal stem cells as a step toward intestinal gene transfer Hum Gene Ther 1994 5: 323–329

    Article  CAS  PubMed  Google Scholar 

  35. Zabner J, Zeiher BG, Friedman E, Welsh MJ . Adenovirus-mediated gene transfer to ciliated airway epithelia requires prolonged incubation time J Virol 1996 70: 6994–7003

    CAS  PubMed  PubMed Central  Google Scholar 

  36. Gao X, Huang L . A novel cationic liposome reagent for efficient transfection of mammalian cells Biochem Biophys Res Commun 1991 179: 280–285

    Article  CAS  PubMed  Google Scholar 

  37. Caplen NJ et al. In vitro liposome-mediated DNA transfection of epithelial cell lines using the cationic liposome DC-Chol/DOPE Gene Therapy 1995 2: 603–613

    CAS  PubMed  Google Scholar 

  38. Caplen NJ et al. Gene therapy for cystic fibrosis in humans by liposome-mediated DNA transfer: the production of resources and the regulatory process Gene Therapy 1994 1: 139–147

    CAS  PubMed  Google Scholar 

  39. Muller DWM et al. Catheter-mediated pulmonary vascular gene transfer and expression Circ Res 1994 75: 1039–1049

    Article  CAS  PubMed  Google Scholar 

  40. Jackson AD et al. A human respiratory-tissue organ culture incorporating an air interface Am J Respir Crit Care Med 1996 153: 1130–1135

    Article  CAS  PubMed  Google Scholar 

  41. Alton EWFW et al. Non-invasive liposome-mediated gene delivery can correct the ion transport defect in cystic fibrosis mutant mice Nat Genet 1993 5: 135–142

    Article  CAS  PubMed  Google Scholar 

  42. Chi K et al. Cyclin A expression in normal and transformed alveolar epithelial cells Am J Respir Cell Mol Biol 1993 9: 115–125

    Article  Google Scholar 

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Kitson, C., Angel, B., Judd, D. et al. The extra- and intracellular barriers to lipid and adenovirus-mediated pulmonary gene transfer in native sheep airway epithelium. Gene Ther 6, 534–546 (1999). https://doi.org/10.1038/sj.gt.3300840

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