Gene transfer into mammalian central nervous system using herpes virus vectors: extended expression of bacterial lacZ in neurons using the neuron-specific enolase promoter

Hum Gene Ther. 1992 Oct;3(5):487-99. doi: 10.1089/hum.1992.3.5-487.

Abstract

A herpes simplex virus (HSV) vector in which the mammalian promoter for neuron-specific enolase (NSE) controls expression of a marker gene was analyzed for its ability to drive expression of this foreign gene in culture and in vivo. In cultured cells, the vector appeared to give neuron-specific expression. Introduction of 10(6) pfu of the virus into the adult rat caudate nucleus by stereotactic injection was not toxic to the animals and yielded beta-galactosidase (beta-gal)-positive neurons for at least 30 days after viral inoculation. This recombinant herpes virus vector is the first described to use a mammalian promoter to yield extended expression of a foreign gene product in the adult mammalian central nervous system (CNS).

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Base Sequence
  • Cell Line
  • Cells, Cultured
  • Central Nervous System / metabolism*
  • Central Nervous System / microbiology
  • DNA, Single-Stranded
  • Genetic Vectors
  • Lac Operon*
  • Molecular Sequence Data
  • Neurons / microbiology
  • Phosphopyruvate Hydratase / genetics*
  • Promoter Regions, Genetic*
  • Rats
  • Simplexvirus / genetics*
  • Transfection*

Substances

  • DNA, Single-Stranded
  • Phosphopyruvate Hydratase