Direct gene transfer into rat articular cartilage by in vivo electroporation

FASEB J. 2003 May;17(8):829-35. doi: 10.1096/fj.02-0518com.

Abstract

To establish a system for efficient direct in vivo gene targeting into rat joint, we have evaluated a strategy of gene transfer by means of the delivery of external electric pulses (EP) to the knee after intra-articular injection of a reporter gene (GFP). Rats were killed at various times after the electro gene-therapy to analyze GFP gene expression by immunohistochemistry. GFP staining was detected in the superficial, middle, and deep zones of the patellar cartilage at days 2 and 9, and thereafter only in the deep zone (months 1 and 2). The average percentage of GFP-positive cells was estimated at 30% both one and 2 months after the gene transfer. Moreover, no pathologic change caused by the EP was detected in the cartilage. The level and stability of the long-term GFP expression found in this study demonstrate the feasibility of a treatment of joint disorders (inflammatory or degenerative, focal or diffuse) using electric gene transfer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cartilage, Articular / metabolism*
  • Electroporation / instrumentation
  • Electroporation / methods*
  • Green Fluorescent Proteins
  • Immunohistochemistry
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Male
  • Microscopy, Fluorescence
  • Plasmids / administration & dosage
  • Plasmids / genetics
  • Rats
  • Rats, Wistar
  • Time Factors
  • Transfection / methods*

Substances

  • Luminescent Proteins
  • Green Fluorescent Proteins