PL EN


Preferencje help
Widoczny [Schowaj] Abstrakt
Liczba wyników

Czasopismo

2000 | 59 | 4 |

Tytuł artykułu

Gene transfer into the central nervous system using Herpes Simplex Virus-1 vectors

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Manipulation of gene expression in developing or in mature central nervous systems (CNS) holds a promise for the resolution of many compelling neurobiological questions, including the feasibility of gene therapy to treat diseases of the brain. In this context, a number of viral vectors have been used in recent years to introduce and express genes into the CNS. This article discusses a gene transfer system based on the Herpes Simplex Virus-1 (HSV-1). We describe here the use of non-replicating, non-toxic HSV-1 vector, 8117/43, in a series of studies carried in our joint program. This vector proves further the utility of HSV-1 as a delivery vehicle to a number of distinct sites within the CNS.

Wydawca

-

Czasopismo

Rocznik

Tom

59

Numer

4

Opis fizyczny

p.221-232,fig.

Twórcy

autor
  • State University of New York, 317 Farber Hall, Buffalo N.Y. 14214, USA
autor
autor
autor
autor
autor
autor

Bibliografia

  • 1. Andersen JK, Garber DA, Meaney CA, and Breakefield XO (1992) Gene transfer into mammalian central nervous system using herpes virus vectors: extended expression of bacterial lacZ in neurons using the neuronspecific enolase promoter. Hum Gene Ther, 3: 487–499.
  • 2. Berthomme H, Lokensgard J, Yang L, Margolis T, and Feldman L T (2000) Evidence for a bidirectional element located downstream from the herpes simplex virus type 1 latency-associated promoter that increases its activity during latency. J Virol, 74: 3613–3622.
  • 3. Bloom DC, Lokensgard JR, Maidment NT, Feldman LT, and Stevens JG (1994) Long-term expression of genes in vivo using non-replicating HSV vectors. Gene Ther, 1: S-36–38.
  • 4. Bloom DC, Maidment NT, Tan A, Dissette VB, Feldman LT, and Stevens JG (1995) Long-term expression of a reporter gene from latent herpes simplex virus in the rat hippocampus. Mol Brain Res, 31: 48–60.
  • 5. Davar G, Kramer M F, Garber D, Roca AL, Andersen JK, Bebrin WDMC, Kosz-Vnenchak M, Knipe DM, and Breakefield XO (1994) Comparative efficacy of expression of genes delivered to mouse sensory neurons with herpes virus vectors. J Comp Neurol, 339: 3–11.
  • 6. Dobson AT, Margolis TP, Sedarati F, Stevens JG, and Feldman LT (1990) A latent, nonpathogenic HSV-1-derived vector stably expresses beta-galactosidase in mouse neurons. Neuron, 5: 353–60.
  • 7. During MJ, Naegele JR, O’Malley KL, and Geller AI (1994) Long-term behavioral recovery in Parkinsonian rats by an HSV vector expressing tyrosine hydroxylase. Science, 266: 1399–1403.
  • 8. Federoff HJ, Geschwind MD, Geller AI, and Kessler JA (1992) Expression of nerve growth factor in vivo from a defective herpes simplex virus 1 vector prevents effects of axotomy on sympathetic ganglia. Proc Natl Acad Sci USA, 89: 1636–1640.
  • 9. Fink DJ, Sternberg LR, Weber PC, Mata M, Goins WF, and Glorioso JC (1992) In vivo expression of beta-galactosidase in hippocampal neurons by HSV-mediated gene transfer. Hum Gene Ther, 3: 11–19.
  • 10. Glorioso JC, Goins WF, and Fink DJ (1992) Herpes simplex virus-based vectors. Sem Virology, 3: 265–276.
  • 11. Kuypers HGJM, and Ugolini G (1990) Viruses as transneuronal tracers. Trends Neurosci, 13: 71–75.
  • 12. Lokensgard JR, Berthomme H, and Feldman LT (1997) The latency-associated promoter of herpes simplex virus type 1 requires a region downstream of the transcription start site for long-term expression during latency. J Virol, 71: 6714–6719.
  • 13. Lokensgard JR, Bloom DC, Dobson AT, and Feldman LT (1994) Long-term promoter activity during herpes simplex virus latency. J Virol, 68: 7148–7158.
  • 14. Margolis TP, Bloom DC, Dobson AT, Feldman LT, and Stevens JG (1993) LAT promoter activity decreases dramatically during the latent phase of ganglionic infection with HSV. Virology, 197: 85–592.
  • 15. Palmer JA, Branston RH, Lilley CE, Robinson MJ, Groutsi F, Smith J, Latchman DS, and Coffin RS (2000) Development and optimization of herpes simplex virus vectors for multiple long-term gene delivery to the peripheral nervous system. J Virol, 74: 5664–5618.
  • 16. Rock DL, and Fraser NW (1985) Latent herpes simplex virus type 1 DNA contains two copies of the virion DNA joint region. J Virol, 55: 849–852.
  • 17. Sedarati F, Margolis TP, and Stevens JG (1993) Latent infection can be established with drastically restricted transcription and replication of the HSV-1 genome. Virology, 192: 687–691.
  • 18. Stevens JG. (1989) Human herpes viruses: a consideration of the latent state. Microbiol Rev, 53: 318–332.
  • 19. Stevens JG, Wagner EK, Devi RGB, Cook ML, and Feldman LT. (1987) RNA complementary to a herpes virus alpha gene mRNA is prominent in latently infected neurons. Science, 235: 1056–1059.
  • 20. Wagner EK, and Bloom DC (1997) Experimental investigation of herpes simplex virus latency. Clin Micro Reviews, 10: 419–443.
  • 21. Wolfe JH, Deshmane SL, and Fraser NW (1992) Herpes virus vector gene transfer and expression of beta-glucuronidase in the central nervous system of MPS VII mice. Nature Gen, 1: 379–384.

Typ dokumentu

Bibliografia

Identyfikatory

Identyfikator YADDA

bwmeta1.element.agro-article-d9042e25-bd49-496b-8fe5-690718a019c9
JavaScript jest wyłączony w Twojej przeglądarce internetowej. Włącz go, a następnie odśwież stronę, aby móc w pełni z niej korzystać.