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The Journal of Neurophysiology Vol. 87 No. 4 April 2002, pp. 2149-2157
Copyright ©2002 by the American Physiological Society
1Department of Pharmacology, 2Department of Neurology, 3Interdepartmental Neuroscience Program, and 4Department of Psychiatry, Yale University School of Medicine, New Haven, Connecticut 06520
White, Benjamin H.,
Theodore R. Cummins,
Daniel H. Wolf,
Stephen G. Waxman,
David S. Russell, and
Leonard K. Kaczmarek.
HSV-1 Helper Virus 5dl1.2 Suppresses Sodium Currents in
Amplicon-Transduced Neurons. J. Neurophysiol. 87: 2149-2157, 2002. The Herpes Simplex Virus-1 (HSV-1)
amplicon system is one of several viral-based strategies currently
being developed for gene delivery into mammalian neurons for
experimental or therapeutic purposes. Amplicon-containing viruses
contain no HSV-1 genes and are amplified in titer relative to the
helper viruses used to package them. In this way, they are designed to
have a minimal impact on the physiology of transduced neurons. We show
here, however, that amplicon preparations made using the 5dl1.2 helper virus selectively suppress sodium currents in cultured neurons by
approximately 80% within 2 days of transduction and reduce average
spike frequency in response to depolarization from 23 ± 4 to
0.4 ± 0.4 Hz. We observe similar suppression of
Na+ currents in cells treated with the 5dl1.2
helper virus alone, indicating that the helper virus retains the
ability of wild-type HSV-1 to inhibit these currents potently. Staining
amplicon-transduced neurons with anti-HSV antibodies, we find that 80%
of the neurons express viral proteins, indicating that helper virus
typically co-infects these cells. We conclude that
Na+ current suppression by the amplicon
preparation results from the preferential coinfection of transduced
neurons by the 5dl1.2 helper virus.
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