JN Watch the video to learn how APS reaches out to developing nations.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 87: 2149-2157, 2002;
0022-3077/02 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by White, B. H.
Right arrow Articles by Kaczmarek, L. K.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by White, B. H.
Right arrow Articles by Kaczmarek, L. K.

The Journal of Neurophysiology Vol. 87 No. 4 April 2002, pp. 2149-2157
Copyright ©2002 by the American Physiological Society

HSV-1 Helper Virus 5dl1.2 Suppresses Sodium Currents in Amplicon-Transduced Neurons

Benjamin H. White,1 Theodore R. Cummins,2 Daniel H. Wolf,3 Stephen G. Waxman,1,2 David S. Russell,2,4 and Leonard K. Kaczmarek1

 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.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online