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Human synapsin 1 gene promoter confers highly neuron-specific long-term transgene expression from an adenoviral vector in the adult rat brain depending on the transduced area

Abstract

Targeting therapeutic transgene expression to defined tissues is a major task in the development of safe and efficient gene therapy protocols. Recombinant adenovirus is an attractive vector because it can be prepared in huge quantity and new generation vectors possess very large cloning capacities combined with reduced immunogenicity. In the brain, adenovirus transduces mainly glial cells, making it difficult to use this vector system in applications that need expression of therapeutic proteins in neurons. Here, we show that by using a small fragment of the human synapsin 1 gene promoter, we were able to restrict transgene expression from an adenoviral vector exclusively to neurons. Furthermore, we obtained stable long-term transgene expression from this vector in striatum and thalamus at appropriate vector dose. Other promoters like the CMV and U1snRNA promoters also mediated transgene expression over several months, but mainly in glial cells. Although the NSE promoter was relatively neuron specific, it still expressed in glial cells also, and was clearly outperformed by the synapsin promoter with respect to transcriptional neuronal targeting. As an important feature of adenoviral-mediated gene transfer to the brain, we demonstrate that dopaminergic neurons of the substantia nigra do not allow for long-term expression from adenoviral vectors. Strikingly, these neurons appeared to specifically attenuate transgene expression by deleting the adenoviral genome.

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References

  1. Björklund A et al. Towards a neuroprotective gene therapy for Parkinson's disease: use of adenovirus, AAV and lentivirus vectors for gene transfer of GDNF to the nigrostriatal system in the rat Parkinson model. Brain Res 2000; 886: 82–98.

    Article  Google Scholar 

  2. Darnell RB . Immunologic complexity in neurons. Neuron 1998; 21: 947–950.

    Article  CAS  Google Scholar 

  3. Kimura T, Griffin DE . The role of CD8(+) T cells and major histocompatibility complex class I expression in the central nervous system of mice infected with neurovirulent Sindbis virus. J Virol 2000;74: 6117–6125.

    Article  CAS  Google Scholar 

  4. Geddes BJ, Harding TC, Lightman SL, Uney JB . Long-term gene therapy in the CNS: reversal of hypothalamic diabetes insipidus in the Brattleboro rat by using an adenovirus expressing arginine vasopressin. Nat Med 1997; 3: 1402–1404.

    Article  CAS  Google Scholar 

  5. Gerdes CA, Castro MG, Lowenstein PR . Strong promoters are the key to highly efficient, noninflammatory and noncytotoxic adenoviral-mediated transgene delivery into the brain in vivo. Mol Ther 2000; 2: 330–338.

    Article  CAS  Google Scholar 

  6. Thomas CE et al. Acute direct adenoviral vector cytotoxicity and chronic, but not acute, inflammatory responses correlate with decreased vector-mediated transgene expression in the brain. Mol Ther 2001; 3: 36–46.

    Article  CAS  Google Scholar 

  7. Navarro V et al. Efficient gene transfer and long-term expression in neurons using a recombinant adenovirus with a neuron-specific promoter. Gene Ther 1999; 6: 1884–1892.

    Article  CAS  Google Scholar 

  8. Millecamps S et al., Neuron-restrictive silencer elements mediate neuron specificity of adenoviral gene expression. Nat Biotechnol 1999; 17: 865–869.

    Article  CAS  Google Scholar 

  9. Miyaguchi K et al. Neuron-targeted gene transfer by adenovirus carrying neural-restrictive silencer element. Neuroreport 1999; 10: 2349–2353.

    Article  CAS  Google Scholar 

  10. Kügler S et al. Neuron-specific expression of therapeutic proteins: evaluation of different cellular promoters in recombinant adenoviral vectors. Mol Cell Neurosci 2001; 17: 78–96.

    Article  Google Scholar 

  11. Kügler S et al. Transduction of axotomized retinal ganglion cells by adenoviral vector administration at the optic nerve stump: an in vivo model system for the inhibition of neuronal apoptotic cell death. Gene Ther 1999; 6: 1759–1767.

    Article  Google Scholar 

  12. Eberhardt O et al. Protection by synergistic effects of adenovirus-mediated X-chromosome-linked inhibitor of apoptosis and glial cell line-derived neurotrophic factor gene transfer in the 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine model of Parkinson's disease. J Neurosci 2000; 20: 9126–9134.

    Article  CAS  Google Scholar 

  13. Rubio N, Martin-Clemente B . Binding of adenovirus to its receptors in mouse astrocytes induces c-fos proto-oncogene and apoptosis. Virology 2002; 297: 211–219.

    Article  CAS  Google Scholar 

  14. Omori N et al. Modification of a fiber protein in an adenovirus vector improves in vitro gene transfer efficiency to the mouse microglial cell line. Neurosci Lett 2002; 324: 145–148.

    Article  CAS  Google Scholar 

  15. Byrnes AP, Wood MJ, Charlton HM . Role of T cells in inflammation caused by adenovirus vectors in the brain. Gene Ther 1996; 3: 644–651.

    CAS  PubMed  Google Scholar 

  16. Amalfitano A, Parks RJ . Separating fact from fiction: assessing the potential of modified adenovirus vectors for use in human gene therapy. Curr Gene Ther 2002;2: 111–133.

    Article  CAS  Google Scholar 

  17. Hsich G, Sena-Esteves M, Breakefield XO . Critical issues in gene therapy for neurologic disease. Hum Gene Ther 2002; 13: 579–604.

    Article  CAS  Google Scholar 

  18. Glover CP et al. Adenoviral-mediated, high-level, cell-specific transgene expression: a syn1-wpre cassette mediates increased transgene expression with no loss of neuron specificity. Mol Ther 2002; 5: 509–516.

    Article  CAS  Google Scholar 

  19. Lesokhin AM, Delgado-Lopez F, Horwitz MS . Inhibition of chemokine expression by adenovirus early region three (E3) genes. J Virol 2002; 76: 8236–8243.

    Article  CAS  Google Scholar 

  20. Isenmann S et al. Intravitreal adenoviral gene transfer evokes an immune response in the retina that is directed against the heterologous lacZ transgene product but does not limit transgene expression. Brain Res 2001; 892: 229–240.

    Article  CAS  Google Scholar 

  21. Fallon JH, Loughlin SE . Substantia nigra, in: PaxÕnos G (ed.) The Rat Nervous System, 2nd ed. Academic Press: San Diego, 1995, pp. 215–237.

    Google Scholar 

  22. Wang Y, Yu L, Geller AI . Diverse stabilities of expression in the rat brain from different cellular promoters in a helper virus-free herpes simplex virus type 1 vector system. Hum Gene Ther 1999; 10: 1763–1771.

    Article  CAS  Google Scholar 

  23. Peel AL et al. Efficient transduction of green fluorescent protein in spinal cord neurons using adeno-associated virus vectors containing cell type- specific promoters. Gene Ther 1997; 4: 16–24.

    Article  CAS  Google Scholar 

  24. Davidson BL et al. Recombinant adeno-associated virus type 2, 4, and 5 vectors: transduction of variant cell types and regions in the mammalian central nervous system. Proc Natl Acad Sci USA 2000; 97: 3428–3432.

    Article  CAS  Google Scholar 

  25. Rabinowitz JE et al. Cross-packaging of a single adeno-associated virus (AAV) type 2 vector genome into multiple AAV serotypes enables transduction with broad specificity. J Virol 2002; 76: 791–801.

    Article  CAS  Google Scholar 

  26. Paxinos G, Watson C . The Rat Brain In Stereotaxic Coordinates, 4th edn. Academiv Press: San Diego, 1998.

    Google Scholar 

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Acknowledgements

We thank Ulrike Schöll for technical assistance. This work was supported in part by the DFG research center Molecular Physiology of the Brain.

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Kügler, S., Kilic, E. & Bähr, M. Human synapsin 1 gene promoter confers highly neuron-specific long-term transgene expression from an adenoviral vector in the adult rat brain depending on the transduced area. Gene Ther 10, 337–347 (2003). https://doi.org/10.1038/sj.gt.3301905

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