Mediation of virion penetration into vascular cells by association of basic fibroblast growth factor with herpes simplex virus type 1 Journal Article


Authors: Baird, A.; Florkiewicz, R. Z.; Maher, P. A.; Kaner, R. J.; Hajjar, D. P.
Article Title: Mediation of virion penetration into vascular cells by association of basic fibroblast growth factor with herpes simplex virus type 1
Abstract: HERPES simplex virus type-1 (HSV-1) is a ubiquitous pathogen that is associated with considerable morbidity in the general population. Although it is known that the virion uses a basic fibroblast growth factor (FGF) receptor to penetrate vascular cells1, it is not known how the viral particle recognizes and binds to this cell surface protein. Here we report that an immunoreactive basic FGF-like protein is associated with the viral particle and that this association appears responsible for viral uptake. Accordingly, HSV-1 infection of Swiss 3T3 cells stimulates the tyrosine phosphorylation of the specific substrate that characterizes the initial cellular response to basic FGF. Antibodies to basic FGF prevent this phosphorylation and inhibit HSV-1 uptake. Because no basic FGF sequence is found in the HSV-1 genome, a model for the infection for some target cells is presented whereby the viral particle uses host cell-derived basic FGF to ensure subsequent infectivity of newly replicated virus. © 1990 Nature Publishing Group.
Keywords: nonhuman; animal; animal tissue; cell line; phosphorylation; animalia; fibroblast growth factor 2; kinetics; recombinant proteins; newborn; simplexvirus; herpes simplex virus 1; herpes; fibroblast growth factor; receptors, cell surface; cricetinae; virion; virus pathogenesis; hamster; human herpesvirus 1; receptors, fibroblast growth factor; priority journal; article; support, non-u.s. gov't; support, u.s. gov't, p.h.s.
Journal Title: Nature
Volume: 348
Issue: 6299
ISSN: 0028-0836
Publisher: Nature Publishing Group  
Date Published: 1990-11-22
Start Page: 344
End Page: 346
Language: English
DOI: 10.1038/348344a0
PUBMED: 2174511
PROVIDER: scopus
DOI/URL:
Notes: Article -- Export Date: 27 January 2020 -- Source: Scopus
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  1. Robert J. Kaner
    14 Kaner