Receptor-mediated targeting of gene delivery vectors: Insights from molecular mechanisms for improved vehicle design

Publisher Website
Google Scholar
Abstract
One way to deliver transgenes to cells in a selective manner is to target the delivery vehicles, or vectors, to specific cell‐surface receptors as a first step toward ulimate transport of the gene to the nucleus for expression. While selective delivery, although often to undesired cell types, occurs naturally for some viral vectors and can be achieved for nonviral vehicles, current understanding and control of the delivery mechanism is inadequate for many therapeutic applications. The complicated nature of receptor‐mediated transgene uptake and transport requires improved analysis to more effectively evaluate delivery vehicles. As receptor‐mediated pathways for gene delivery typically involve vector binding, internalization, subcellular trafficking, vesicular escape, nuclear translocation, and unpackaging for transcription, each of these processes offer mechanisms that can be exploited to enhance targeted gene delivery via properly designed vehicles. For the purpose of this review, current targeted gene delivery vehicles are divided into three approaches: viral, synthetic, and hybrid vectors. Each approach possesses advantages as well as disadvantages at the present time for in vitro and in vivo application, and provides particular challenges to overcome in order to gain significantly improved targeted delivery properties. Quantitative experiments and mathematical modeling of the gene delivery pathway will serve to provide insight into molecular mechanisms and rate‐limiting steps for effective gene expression. Information on molecular mechanisms obtained by such methodologies can then be applied to specific vectors, whether viral, synthetic, or hybrid, allowing for the creation of targeted, effective, and safe gene therapeutics. © 2000 John Wiley & Sons, Inc. Biotechnol Bioeng 70: 593–605, 2000.