Cardiac Gene Expression pp 343-355

Part of the Methods in Molecular Biology book series (MIMB, volume 366)

Lentivirus-Mediated Gene Expression

  • Jing Zhao
  • Andrew M. L. Lever

Abstract

Lentiviruses have the capacity to enter and integrate their genetic material into cells that are not dividing. This property is retained in vectors based on these agents. They can thus effect gene delivery to cells that are difficult to transduce such as cardiac myocytes in vitro and in vivo. They are also relatively efficient at entering dividing cells and can transduce stem cells and vascular endothelium. They have a substantial gene-carrying capacity of up to around 9 kb. They do not trigger an inflammatory response and are thus useful when proinflammatory agents are undesirable, such as in transplantation. Their ease of cloning and well-understood molecular biology have made them highly suitable for gene delivery to the heart.

Key Words

Lentiviral vector HIV-1 vector gene therapy gene transfer transduction 293T cells cardiomyocytes, heart 

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Copyright information

© Humana Press Inc. 2007

Authors and Affiliations

  • Jing Zhao
    • 1
  • Andrew M. L. Lever
    • 1
  1. 1.Department of Medicine, Addenbrooke’s HospitalUniversity of CambridgeCambridgeUK

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