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.

  • Research Article
  • Published:

A single adenovirus vector mediates doxycycline-controlled expression of tyrosine hydroxylase in brain grafts of human neural progenitors

Abstract

Ex vivo gene transfer is emerging as a promising therapeutic approach to human neurodegenerative diseases. By combining efficient methodologies for cell amplification and gene delivery, large numbers of cells can be generated with the capacity to synthesize therapeutic molecules. These cells can then be transplanted into the degenerating central nervous system (CNS). Applying this approach to human diseases will require the development of suitable cellular vehicles, as well as safe gene delivery systems capable of tightly controlled transgene expression. For such brain repair technologies, human neural progenitors may be extremely valuable, because of their human CNS origin and developmental potential. We have used these cells to develop a system for the regulated expression of a gene of therapeutic potential. We report the construction of a single adenovirus encoding human tyrosine hydroxylase 1 (hTH-1) under the negative control of the tetracycline-based gene regulatory system. Human neural progenitors infected with this vector produced large amounts of hTH-1. Most importantly, doxycycline allowed a reversible switch of transgene transcription both in vitro and in vivo. This system may be applied to the development of therapies for human neurodegenerative diseases.

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: AdPGK♦tet♦hTH-1.
Figure 2: (A) Infection of human neural progenitors with AdPGK♦tet♦hTH-1 at various MOIs.
Figure 3: Kinetics of clearance (A) and resumption (B) of hTH activity from cultures infected with AdPGK♦tet♦hTH-1 (MOI = 40) after addition (A) or withdrawal (B) of doxycycline (5 ng/ml) on day 0 (5.5 days after infection).
Figure 4: TH immunoreactivity (brown immunoperoxidase staining) in intrastriatal grafts of human neural progenitors infected with AdPGK♦tet♦hTH-1 (MOI = 40).
Figure 5: TH expression in grafts of human neural progenitors infected with AdPGK♦tet♦hTH-1 (MOI = 40), as determined by anti-TH immunohistochemistry (brown immunoperoxidase staining) and in situ hybridization using a [35S]-labeled hTH-1 specific antisense oligonucleotide (black silver grains) on 15 μm cryostat brain sections from (A) an untreated animal and (B) an animal treated daily with 1 mg/ml doxycycline.
Figure 6: TH expression in grafts of human neural progenitors infected with AdPGK♦tet♦hTH-1 as determined by immunohistochemistry (A–D) or in situ hybridization using an oligonucleotide probe labeled with digoxygenin-tagged rUTP (E–G).

Similar content being viewed by others

References

  1. Marsden, C.D. & Parkes, J.D. "On-off" effects in patients with Parkinson's disease on chronic levodopa therapy. Lancet 1, 292–296 (1976).

    Article  CAS  Google Scholar 

  2. Lindvall, O. Neural transplantation: a hope for patients with Parkinson's disease. Neuroreport 8, iii–x ( 1997).

    Article  CAS  Google Scholar 

  3. Raymon, H.K., Thode, S. & Gage, F.H. Application of ex vivo gene therapy in the treatment of Parkinson's disease. Exp. Neurol. 144, 82 –91 (1997).

    Article  CAS  Google Scholar 

  4. Horellou, P., Sabate, O., Buc-Caron, M.H. & Mallet, J. Adenovirus-mediated gene transfer to the central nervous system for Parkinson's disease. Exp. Neurol. 144, 131– 138 (1997).

    Article  CAS  Google Scholar 

  5. Uchida, K. & Kohsaka, S. Current advances in neural transplantation. Human Cell 2, 150–155 (1989).

    CAS  PubMed  Google Scholar 

  6. Wolff, J.A. et al. Grafting fibroblasts genetically modified to produce L-dopa in a rat model of Parkinson disease. Proc. Natl. Acad. Sci. USA 86 , 9011–9014 (1989).

    Article  CAS  Google Scholar 

  7. Horellou, P., Brundin, P., Kalen, P., Mallet, J. & Björklund, A. In vivo release of dopa and dopamine from genetically engineered cells grafted to the denervated rat striatum. Neuron 5, 393–402 ( 1990).

    Article  CAS  Google Scholar 

  8. Fisher, L.J., Jinnah, H.A., Kale, L.C., Higgins, G.A. & Gage, F.H. Survival and function of intrastriatally grafted primary fibroblasts genetically modified to produce L-dopa. Neuron 6, 371–380 (1991).

    Article  CAS  Google Scholar 

  9. Whittemore, S.R., Eaton, M.J. & Onifer, S.M. Gene therapy and the use of stem cells for central nervous system regeneration. Adv. Neurol. 72, 113–119 (1997).

    CAS  PubMed  Google Scholar 

  10. Martinez, S.A. & Björklund, A. Immortalized neural progenitor cells for CNS gene transfer and repair. Trends Neurosci. 20, 530–538 ( 1997).

    Article  Google Scholar 

  11. Fisher, L.J. Neural precursor cells: applications for the study and repair of the central nervous system. Neurobiol. Dis. 4, 1– 22 (1997).

    Article  CAS  Google Scholar 

  12. Groves, A.K. et al. Repair of demyelinated lesions by transplantation of purified O-2A progenitor cells. Nature 362, 453– 455 (1993).

    Article  CAS  Google Scholar 

  13. Snyder, E.Y., Taylor, R.M. & Wolfe, J.H. Neural progenitor cell engraftment corrects lysosomal storage throughout the MPS VII mouse brain. Nature 374, 367–370 (1995).

    Article  CAS  Google Scholar 

  14. Buc, C.M. Neuroepithelial progenitor cells explanted from human fetal brain proliferate and differentiate in vitro. Neurobiol. Dis. 2, 37–47 (1995).

    Article  Google Scholar 

  15. Sabate, O. et al. Transplantation to the rat brain of human neural progenitors that were genetically modified using adenoviruses. Nat. Genet. 9, 256–260 (1995).

    Article  CAS  Google Scholar 

  16. Miller, N. & Whelan, J. Progress in transcriptionally targeted and regulatable vectors for genetic therapy. Hum. Gene Ther. 8, 803–815 (1997).

    Article  CAS  Google Scholar 

  17. Obeso, J.A., Grandas, F., Herrero, M.T. & Horowski, R. The role of pulsatile versus continuous dopamine receptor stimulation for functional recovery in Parkinson's disease. Eur. J. Neurosci. 6, 889–897 (1994).

    Article  CAS  Google Scholar 

  18. Saez, E., No, D., West, A. & Evans, R.M. Inducible gene expression in mammalian cells and transgenic mice. Curr. Opin. Biotechnol. 8, 608–616 ( 1997).

    Article  CAS  Google Scholar 

  19. Gossen, M. & Bujard, H. Tight control of gene expression in mammalian cells by tetracycline-responsive promoters. Proc. Natl. Acad. Sci .USA 89, 5547–5551 (1992).

    Article  CAS  Google Scholar 

  20. Gossen, M. et al. Transcriptional activation by tetracyclines in mammalian cells. Science 268, 1766–1769 ( 1995).

    Article  CAS  Google Scholar 

  21. Corti, O., Horellou, P., Colin, P., Cattaneo, E. & Mallet, J. Intracerebral tetracycline-dependent regulation of gene expression in grafts of neural precursors. Neuroreport 7, 1655–1659 (1996).

    Article  CAS  Google Scholar 

  22. Mayford, M. et al. Control of memory formation through regulated expression of a CaMKII transgene. Science 274, 1678– 1683 (1996).

    Article  CAS  Google Scholar 

  23. Yu, J.S., Sena, E.M., Paulus, W., Breakefield, X.O. & Reeves, S.A. Retroviral delivery and tetracycline-dependent expression of IL-1beta-converting enzyme (ICE) in a rat glioma model provides controlled induction of apoptotic death in tumor cells. Cancer Res. 56, 5423–5427 (1996).

    CAS  PubMed  Google Scholar 

  24. Adra, C.N., Boer, P.H. & McBurney, M.W. Cloning and expression of the mouse pgk-1 gene and the nucleotide sequence of its promoter. Gene 60, 65–74 (1987).

    Article  CAS  Google Scholar 

  25. McGeady, M.L., Wood, T.G., Maizel, J.V. & Vande, W.G. Sequences upstream from the mouse c-mos oncogene may function as a transcription termination signal. DNA 5, 289–298 (1986).

    Article  CAS  Google Scholar 

  26. Ungerstedt, U. & Arbuthnott, G.W. Quantitative recording of rotational behavior in rats after 6-hydroxydopamine lesions of the nigrostriatal dopamine system. Brain Res. 24, 485–493 (1970).

    Article  CAS  Google Scholar 

  27. Harding, T.C., Geddes, B.J., Murphy, D., Knight, D. & Uney, J.B. Switching transgene expression in the brain using an adenoviral tetracycline-regulatable system. Nat. Biotechnol. 16 , 553–555 (1998).

    Article  CAS  Google Scholar 

  28. StLouis, D. & Verma, I.M. An alternative approach to somatic cell gene therapy. Proc. Natl. Acad. Sci. USA 85, 3150–3154 (1988).

    Article  CAS  Google Scholar 

  29. Scharfmann, R., Axelrod, J.H. & Verma, I.M. Long-term in vivo expression of retrovirus-mediated gene transfer in mouse fibroblast implants. Proc. Natl. Acad. Sci. USA 88, 4626–4630 ( 1991).

    Article  CAS  Google Scholar 

  30. Palmer, T.D., Rosman, G.J., Osborne, W.R. & Miller, A.D. Genetically modified skin fibroblasts persist long after transplantation but gradually inactivate introduced genes. Proc. Natl. Acad. Sci. USA 88, 1330–1334 ( 1991).

    Article  CAS  Google Scholar 

  31. Kay, M.A. et al. Expression of humans alpha 1-antitrypsin in dogs after autologous transplantation of retroviral transduced hepatocytes. Proc. Natl. Acad. Sci. USA 89, 89–93 ( 1992).

    Article  CAS  Google Scholar 

  32. Lim, B., Apperley, J.F., Orkin, S.H. & Williams, D.A. Long-term expression of human adenosine deaminase in mice transplanted with retrovirus-infected hematopoietic stem cells. Proc. Natl. Acad. Sci. USA. 86, 8892–8896 (1989).

    Article  CAS  Google Scholar 

  33. Moullier, P., Marechal, V., Danos, O. & Heard, J.M. Continuous systemic secretion of a lysosomal enzyme by genetically modified mouse skin fibroblasts. Transplantation 56, 427– 432 (1993).

    Article  CAS  Google Scholar 

  34. Kaplitt, M.G. et al. Preproenkephalin promoter yields region-specific and long-term expression in adult brain after direct in vivo gene transfer via a defective herpes simplex viral vector. Proc. Natl. Acad. Sci. USA 91, 8979–8983 (1994).

    Article  CAS  Google Scholar 

  35. Kojima, H. et al. Adenovirus-mediated transduction with human glial cell line-derived neurotrophic factor gene prevents 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced dopamine depletion in striatum of mouse brain. Biochem. Biophys. Res. Commun. 238, 569–573 (1997).

    Article  CAS  Google Scholar 

  36. Geny, C. et al. Long-term delayed vascularization of human neural transplants to the rat brain. J. Neurosci. 14, 7553– 7562 (1994).

    Article  CAS  Google Scholar 

  37. Kistner, A. et al. Doxycycline-mediated quantitative and tissue-specific control of gene expression in transgenic mice. Proc. Natl. Acad. Sci. USA 93, 10933–10938 ( 1996).

    Article  CAS  Google Scholar 

  38. A-Mohammadi, S., Alvarez, V.L., Ashworth, L.J. & Hawkins, R.E. Delay in resumption of the activity of tetracycline-regulatable promoter following removal of tetracycline analogues. Gene. Ther. 4, 993–997 (1997).

    Article  CAS  Google Scholar 

  39. Brundin, P. et al. Human fetal dopamine neurons grafted in a rat model of Parkinson's disease: immunological aspects, spontaneous and drug-induced behaviour, and dopamine release. Exp. Brain. Res. 70, 192 –208 (1988).

    CAS  PubMed  Google Scholar 

  40. Freese, A. et al. Phenotypic recovery in parkinsonian rats: relationship between numbers of transduced cells and behavior using an adenoviral vector expressing tyrosine hydroxylase. Society for Neuroscience, Abstracts 23 , 540 (1997).

    Google Scholar 

  41. Pedersen, E.B., Zimmer, J. & Finsen, B. Triple immunosuppression protects murine intracerebral, hippocampal xenografts in adult rat hosts: effects on cellular infiltration, major histocompatibility complex antigen induction and blood-brain barrier leakage. Neuroscience 78, 685– 701 (1997).

    Article  CAS  Google Scholar 

  42. Stratford, P.L., Makeh, I., Perricaudet, M. & Briand, P. Widespread long-term gene transfer to mouse skeletal muscles and heart. J. Clin. Invest. 90, 626–630 (1992).

    Article  Google Scholar 

  43. Reinhard, J.J., Smith, G.K. & Nichol, C.A. A rapid and sensitive assay for tyrosine-3-monooxygenase based upon the release of 3[H2O] and adsorption of [3H]-tyrosine by charcoal. Life Sci. 39, 2185–2189 (1986).

    Article  CAS  Google Scholar 

  44. Dumas, S., Horellou, P., Helin, C. & Mallet, J. Co-expression of tyrosine hydroxylase messenger RNA 1 and 2 in human ventral mesencephalon revealed by digoxigenin- and biotin-labelled oligodeoxyribonucleotides. J. Chem. Neuroanat. 5, 11–18 (1992).

    Article  CAS  Google Scholar 

  45. Lanièce, P. et al. A novel rat tyrosine hydroxylase mRNA species generated by alternative splicing. J. Neurochem. 66, 1819– 1825 (1996).

    Article  Google Scholar 

Download references

Acknowledgements

We thank Gilles Pitiot for helpful discussions and critical review of the manuscript. We also thank Amelia Sanchez-Capelo for her unremitting contribution to the construction of AdPGK♦tet♦hTH-1. We thank Novartis for generously providing cyclosporine A. This work was supported by grants from the Association Francaise contre les Myopathies, the Centre National de la Recherche Scientifique, the Conséil Régional d'Ile de France, EC contract No. 951012, the European Science Foundation, the Institut pour la Recherche sur la Moelle Epiniere and Retina France.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jacques Mallet.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Corti, O., Sabaté, O., Horellou, P. et al. A single adenovirus vector mediates doxycycline-controlled expression of tyrosine hydroxylase in brain grafts of human neural progenitors. Nat Biotechnol 17, 349–354 (1999). https://doi.org/10.1038/7901

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1038/7901

This article is cited by

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing