Evidence for disease-regulated transgene expression in the brain with use of lentiviral vectors

J Neurosci Res. 2006 Jul;84(1):58-67. doi: 10.1002/jnr.20872.

Abstract

In this study we have developed and validated a novel approach of transgene regulation in the brain. By using lentiviral vectors that incorporate promoters of genes that are up-regulated during different pathological states, we were able to regulate transgene expression in accordance with the disease process. When using a glial fibrillary acidic protein promoter, efficient disease regulation in glial cells was achieved after an excitotoxic lesion or a 6-hydroxydopamine (6-OHDA) lesion. Transgene expression was physiologically regulated and displayed a dose-dependent increase depending on the severity of lesion. Efficient regulation was also achieved in neurons when using a preproenkephlin promoter in 6-OHDA-lesioned rats, allowing combined regulation and targeting. This disease-regulated approach allows control of transgene expression in the brain without the use of inducer molecules and without overexpression of transactivator proteins.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified
  • Brain / metabolism*
  • Brain / virology
  • Brain Injuries / chemically induced
  • Brain Injuries / physiopathology*
  • Functional Laterality
  • Gene Expression Regulation / drug effects
  • Gene Expression Regulation / physiology*
  • Genetic Vectors / physiology*
  • Glial Fibrillary Acidic Protein / genetics
  • Glial Fibrillary Acidic Protein / metabolism
  • Green Fluorescent Proteins / biosynthesis
  • Humans
  • Ibotenic Acid / toxicity
  • Immunohistochemistry / methods
  • Lentivirus / physiology*
  • Nerve Tissue Proteins / metabolism
  • Oxidopamine / toxicity
  • Promoter Regions, Genetic / physiology
  • RNA, Messenger / metabolism
  • Rats
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Time Factors
  • beta-Galactosidase / metabolism

Substances

  • Glial Fibrillary Acidic Protein
  • Nerve Tissue Proteins
  • RNA, Messenger
  • Green Fluorescent Proteins
  • Ibotenic Acid
  • Oxidopamine
  • beta-Galactosidase