Abstract
Gene therapy is an attractive approach for the treatment of a number of inherited and acquired disorders of the nervous system. For instance, genetic manipulations could be used to provide locally the neurotransmitters that are defective in conditions such as Parkinson’s disease, or to produce healing levels of growth factors to protect neurons against the irreversible consequences of traumatic or degenerative lesions.
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References
Mulligan, R. C. (1993) The basic science of gene therapy. Science 260, 926–932.
Trono, D. (1995) HIV accessory proteins: leading roles for the supporting cast. Cell 82, 189–192.
Varmus, H. (1988) Retroviruses. Science 240, 1427–1435.
Humphries, E. H. and Temin, H. M. (1972) Cell cycle dependent activation of Rous sarcoma virus-infected stationary chicken cells: avian leukosis virus group-specific antigens and ribonucleic acid. J. Virol. 10, 82–87.
Humphries, E. H. and Temin, H. M. (1974) Requirement for cell division for initiation of transcription of Rous sarcoma virus RNA. J. Virol. 14, 531–546.
Roe, T., Reynolds, T. C., Yu, G., and Brown, P. O. (1993) Integration of murine leukemia virus DNA depends on mitosis. EMBO J. 12, 2099–2108.
Lewis, P. F. and Emerman, M. (1994) Passage through mitosis is required for oncoretroviruses but not for the human immunodeficiency virus. J. Virol. 68, 510–516.
Lewis, P., Hensel M. and Emerman, M. (1992) Human immunodeficiency virus infection of cells arrested in the cell cycle. EMBO J. 11, 3053–3058.
Bukrinsky, M. I., Sharova, N., Dempsey, M. P., Stanwick, T. L., Bukrinskaya, A. G., Haggerty, S. and Stevenson, M. (1992) Active nuclear import of human immunodeficiency virus type 1 preintegration complexes. Proc. Natl. Acad. Sci. USA 89, 6580–6584.
Gallay, P., Stitt, V., Mundy, C., Oettinger, M., and Trono, D. (1996) Role of the karyopherin pathway in human immunodeficiency virus type 1 nuclear import. J. Virol. 70, 1027–1032.
Bukrinsky, M. I., Haggerty, S., Dempsey, M. P., Sharova, N., Adzhubei, A., Spitz, L., et al. (1993) A nuclear localization signal within HIV-1 matrix protein that governs infection of non-dividing cells. Nature 365, 666–669.
Heinzinger, N. K., Bukrinsky, M. I., Haggerty, S. A., Ragland, A. M., Kewalramani, V., Lee, M.-A., et al. (1994) The Vpr protein of human immunodeficiency virus type 1 influences nuclear localization of viral nucleic acids in nondividing host cells. Proc. Natl. Acad. Sci. USA 91, 7311–7315.
von Schwedler, U., Kornbluth, R. S., and Trono, D. (1994) The nuclear localization signal of the matrix protein of human immunodeficiency virus type 1 allows the establishment of infection in macrophages and quiescent T lymphocytes. Proc. Natl. Acad. Sci. USA 91, 6992–6996.
Gallay, P., Naldini, L., Blömer, U., Chin, D., Verma, I. M., Gage, F., Hope, T., and Trono, D. (1997) HIV-1 infection of nondividing cells can be mediated through the recognition of integrase by the importin/karyopherin pathway. Proc. Natl. Acad. Sci. USA (in press).
Gallay, P., Swingler, S., Aiken, C., and Trono, D. (1995) HIV-1 infection of nondividing cells: C-terminal phosphorylation of the viral matrix protein is a key regulator. Cell 80, 379–388.
Gallay, P., Swingler, S., Song, J., Bushman, F., and Trono, D. (1995) HIV-1 nuclear import is governed by the phosphotyrosine-mediated binding of matrix to the core domain of integrase. Cell 83, 569–576.
Whittaker, G., Bui, M., and Helenius, A. (1996) The role of nuclear import and export in influenza virus infection. Trends Cell Biol. 6, 67–71.
Greber, U. F. and Kasamatsu, H. (1996) Nuclear targeting of SV 40 and adenovirus. Trends Cell. Biol. 6, 189–195.
Naldini, L., Blömer, U., Gallay, P., Ory, D., Mulligan, R. C., Gage, F. H., Verma, I. M., and Trono, D. (1996) In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector. Science 272, 263–267.
Naldini, L., Blömer, U., Gage, F. H., Trono, D., and Verma, I. M. (1996) Efficient transfer, integration, and long-term sustained expression of the transgene in adult rat brains injected with a lentiviral vector. Proc. Natl. Acad. Sci. USA 93, 11382–11388.
Burns, J. C., Friedman, T., Criever, W., Burrascano, M., and Yee, J.-K. (1993) Vesicular stomatitis virus G glycoprotein pseudotyped retroviral vectors: concentration to very high titer and efficient gene transfer into mammalian and nonmammalian cells. Proc. Natl. Acad. Sci. USA 90, 8033–8037.
Zhang, H., Dornadula, G., and Pomerantz, R. J. (1996) Endogenous reverse transcription of human immunodeficiency virus type 1 in physiological microenvironments: an important stage for viral infection in nondividing cells. J. Virol. 70, 2809–2824.
Miller, D. G., Adam, M. A., and Miller, A. D. (1990) Gene transfer by retrovirus vectors occurs only in cells that are actively replicating at the time of infection. Mol. Cell. Biol. 10, 4239–4242.
Zack, J. A., Arriso, S. J., Weitsman, S. R., Go, A. S., Haislip, A., and Chen, I. S. (1990) Hiv.1 entry into quiescent primary lymphocytes: molecular analysis reveals a labile, latent viral structure. Cell 61, 213–222.
Meyerhans, A., Vartanian, J.-P., Hultgren, C., Plikat, U., Karlsson, A., Wang, L., Eriksson, S., and Waion-Hobson, S. (1994) Restriction and enhancement of human immunodeficiency virus type 1 replication by modulation of intracellular deoxynucleoside triphosphate pools. J. Virol. 68, 535–540.
Schuitemaker, H., Koostra, N. A., Fouchier, R. A. M., Hooibrink, B., and Miedeam, F. (1994) Productive HIV-1 infection of macrophages restricted to the cell fraction with proliferative capacity. EMBO J. 13, 5929–5936.
Coffin, J. M. (1990) Retroviridae and their replication, in Virology, ( Fields, B. N., Knipe, D. M., and Howry, P. M. eds.). Raven, New York, pp. 1437–1500.
Blömer, U., Naldini, L., Kafri, T., Trono, D., Verma, I. M., and Gage, F. H. (1997) Highly efficient and sustained gene transfer in adult neurons with a lentiviral vector. J. Virol. (in press)
Wagner, R. R. (1987) Rhabdovirus biology and infection: An overview, in The Rhabdoviruses ( Wagner, R. R., ed.), Plenum, New York, pp. 9–74.
Baskar, J. F., Smith, P. P., Nilaver, G., Jupp, R. A., Hoffman, S., Peffer, N. J., et al. (1996) Developmental analysis of the cytomegalovirus enhancer in transgenic animals. J. Virol. 70, 3207–3214.
Zuffrey, R., Napy, D., Mandai, R. J., Naldini, L., and Trono, D. (1997) Multiply attenuated lentiviral vector achieves efficient gene delivery in vivo. Nature Biotech. (in press).
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Trono, D., Blömer, U., Naldini, L. (1998). Lentiviral Vectors for Gene Delivery in the Nervous System. In: Chiocca, E.A., Breakefield, X.O. (eds) Gene Therapy for Neurological Disorders and Brain Tumors. Contemporary Neuroscience. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-478-8_7
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DOI: https://doi.org/10.1007/978-1-59259-478-8_7
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