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Fusogenic effects of murine retroviruses and cationic enhancers of transduction

Abstract

The maturation of retrovirus particles involves proteolytic cleavage of the envelope glycoprotein transmembrane component, resulting in conversion of the virus particle to a fusogenic or infectious state. Susceptible murine cells exposed to virus-containing supernatants from ecotropic retroviral helper cells occasionally fused to neighboring cells, resulting in syncytia (giant cells with multiple nuclei). Polycationic molecules dramatically enhanced the effect, leading to widespread cell death. The degree of cell fusion was dependent upon the retroviral envelope subtype (ecotropic→amphotropic, gibbon ape leukemia virus was negative) as well as on the polycationic reagent used (G9 dendrimer→Lipofectamine→polybrene). Cell fusion effects were not mediated by the retroviral vector backbone, because virus-containing supernatants from helper cells (without vector) and vector producer cells had a similar effect. Human target cells were not fused by any type of murine retrovirus; in addition, amphotropic virus from human helper cells was not fusogenic toward murine cells. Thus, fusogenic effects were important during the propagation of vectors using murine helper cells but were not a significant factor during the transduction of human cells.

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Correspondence to Clague P Hodgson.

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Xu, G., Solaiman, F., Zink, M. et al. Fusogenic effects of murine retroviruses and cationic enhancers of transduction. Cancer Gene Ther 7, 53–58 (2000). https://doi.org/10.1038/sj.cgt.7700095

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  • DOI: https://doi.org/10.1038/sj.cgt.7700095

Keywords

  • Retrovirus
  • vector
  • gene therapy
  • syncytia
  • cell fusion.

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