Differences in resistance to herpes simplex virus type 1 (HSV-1) among oligodendroglia derived from different strains of mice are determined after viral adsorption but prior to the expression of immediate early (IE) genes

References

• Anderson R G W, Brown M S, Goldstein J L. Role of the coated endocytic vesicle in the uptake of receptor‐bound low density lipoprotein in human fibroblasts. Cell 1977; 10: 351–364
   PubMed Web of Science ®Google Scholar
• Bergstrom T, Conradi N, Hansson E, Liljeroth A, Vahlne A. Resistance of rat CNS to brainsteminfection with Herpes Simplex Virus type 1. Acta Neuropathol 1994; 87: 398–404
   Google Scholar
• Cassai E N, Sarmiento M, Spear P. Comparison of the virion proteins specified by herpes simplex virus types 1 and 2. Journal of Virology 1987; 61: 1327–1331
   Google Scholar
• Cook M L, Stevens J G. Pathogenesis of herpetic neuritis and ganglionitis in mice: Evidence for intra‐axonal transport of infection. Infection and Immunity 1973; 7: 272–288
   PubMed Web of Science ®Google Scholar
• Fraser N W, Valyi‐Nagy T. Viral, neuronal and immunefactors which may influence herpes simplex virus (HSV) latency and reactivation. Microbial Pathogenesis 1993; 15: 83–91
   Google Scholar
• Fuller O, Spear P. Anti‐glycoprotein D antibodies that permit adsorption but block infection by herpes simplex virus 1 prevent virion‐cell fusion at the cell surface. Proceedings of the National Academy of Sciences, USA, 1987; 84: 5454–5458
   Google Scholar
• Herold B C, Visalli R R, Susmarski N, Brandt C R, Spear P G. Glycoprotein C‐independent binding of herpes simplex virus to cells requires cell surface heparan sulphate and glycoprotein B. Journal of General Virology 1994; 75: 1211–1222
   PubMed Web of Science ®Google Scholar
• Highlander S L, Sutherland S L, Gage P J, Johnson D C, Levine M, Glorioso J C. Neutralizing monoclonal antibodies specific for herpes simplex virus glycoprotein D inhibit virus penetration. Journal of Virology 1987; 61: 3356–3364
   PubMed Web of Science ®Google Scholar
• Honess R W, Roizman B. Regulation of herpesvirus macrdmolecular synthesis. 1. Cascade regulation of the synthesis of three groups of viral proteins. Journal of Virology 1974; 14: 8–19
   PubMed Web of Science ®Google Scholar
• Huang A S, Wagner R R. Penetration of herpes simplex virus into human epidermoid cells. Proceedings of the Society for Experimental Biology and Medicine 1964; 116: 863–869
   Google Scholar
• Kastrukoff L F, Hamada T, Schumacher U, Long C, Doherty P, Koprowski H. Central nervous system infection, latency, and immune responses in Herpes Simplex Type 1 infections in mice. Journal of Neuroimmunology 1982; 2: 295–305
   Google Scholar
• Kastrukoff L F, Lau A, Puterman M L. Genetics of natural resistance to herpes simplex virus type 1 latent infection in the peripheral system in mice. Journal of General Virology 1986; 67: 613–621
   PubMedGoogle Scholar
• Kastrukoff L F, Lau A, Kim S U. Multifocal CNS demyelination following peripheral inoculation with herpes simplex virus type 1. Annals of Neurology 1987; 22: 52–59
   Google Scholar
• Kastrukoff L F, Lau A, Thomas E E. Mechanisms mediating differences in resistance of murine oligodendrocytes (OL) derived from inbred strains of mice to Herpes simplex virus type 1 (HSV 1). Annals of Neurology 1988; 24: 147
   Google Scholar
• Kastrukoff L F, Lau A, Leung G, Thomas E E. Herpes simplex type 1 (HSV 1) induced multifocal central nervous system (CNS) demyelination (CNS) in mice. Journal of Neuropathology & Experimental Neurology 1992; 51: 432–439
   Google Scholar
• Kim S U, Sato Y, Silberberg D M. Long‐term culture of human oligodendrocytes. Journal of Neurological Science 1983; 62: 295–301
   PubMedGoogle Scholar
• Kristensson K, Svennerholm B, Vahlne A, Nilheden E, Persson L. Virus‐induced demyelination in herpes simplex virus‐infected mice. Journal of Neurological Science 1982; 53: 205–216
   PubMedGoogle Scholar
• Lycke E, Johansson M, Svennerhol B, Lindahl U. Binding of herpes simplex virus to cellular heparan sulphate, an initial step in the adsorption process. Journal of General Virology 1991; 72: 1131–1137
   PubMed Web of Science ®Google Scholar
• McKendall R R. Herpes simplex virus diseases. Handbook of Neurovirology, R R McKendall, W G Stroop. Marcel Dekker, Inc., New York 1994; 253–267
   Google Scholar
• Mester J C, Rouse B T. The mouse model and understanding immunity to herpes simplex virus. Reviews of Infectious Diseases 1992; 13: S935–S945
   Google Scholar
• Rinaman L, Card J P, Enquist L W. Spatiotemporal responses of astrocytes, ramified microglia and brain macrophages to central neuronal infection with pseudorabies virus. Journal of Neuroscience 1993a; 13: 685–702
   Google Scholar
• Rinaman L, Lynn R B, Le B H, Meade R P, Miselis R R, Enquist L W. Pseudorabies virus infection of the rat central nervous system: Ultrastructural characterization of viral replication, transport and pathogenesis. Journal of Neuroscience 1993b; 13: 2515–2539
   Google Scholar
• Sarmiento M, Haffey M, Spear P. Membrane proteins specified by herpes simplex viruses. III. Role of glycoprotein VP7 (B2) in virion infectivity. Journal of Virology 1979; 29: 1149–1158
   PubMed Web of Science ®Google Scholar
• Shieh M ‐T, Spear P G. Herpesvirus‐induced cell fusion that is independent on cell surface heparan sulphate or soluble heparin. Journal of Virology 1994; 68: 1224–1228
   PubMed Web of Science ®Google Scholar
• Spear P, Roizman B. Proteins specified by herpes simplex virus. V. Purification and structural proteins of the herpes virus virion. Journal of Virology 1972; 9: 143
   PubMed Web of Science ®Google Scholar
• Spear P G, Wittels M. Herpes simplex virus: Pathway into cells. Cell Biology of Virus Entry, Replication, and Pathogenesis, R Compans, A Helenius, B A Oldstone. Alan R. Liss, Inc., New York 1989; 163–175
   Google Scholar
• Spear P G. Membrane fusion induced by herpes simplex virus. Viral Fusion Mechanisms, J Bentz. CRC Press Inc., Boca Raton, Florida 1992; 210–232
   Google Scholar
• Stevens J G. HSV‐1 neuroinvasiveness. Intervirology 1993; 35: 152–163
   Google Scholar
• Svennerholm B, Vahlne A, Lycke E. Early interactions of herpes simplex virus with mouse peritoneal macrophages. Infection and Immunity 1982; 37: 907–911
   Google Scholar
• Thomas E E, Lau A S, Kim S U, Osborne D, Kastrukoff L F. Variation in resistance to herpes simplex virus type 1 of oligodendrocytes derived from inbred strains of mice. Journal of General Virology 1991; 72: 2051–2057
   PubMed Web of Science ®Google Scholar
• Ugolini G, Kuypers P, Strick P. Transneuronal transfer of herpes virus from peripheral nerves to cortex and brainstem. Science 1989; 243: 89–91
   PubMed Web of Science ®Google Scholar
• Wittels M, Spear P G. Penetration of cells by herpes simplex virus does not require a low pH‐dependent endocytotic pathway. Virus Research 1991; 18: 271–290
   Google Scholar
• WuDunn D, Spear P G. Initial interaction of herpes simplex virus with cells is binding to heparan sulphate. Journal of Virology 1989; 63: 52–58
   PubMed Web of Science ®Google Scholar
• Wu L, Morahan S. Macrophages and other non specific defences: Role in modulating resistance against herpes simplex virus. Current Topics in Microbiology and Immunology 1992; 179: 89–107
   PubMedGoogle Scholar
• Yuhasz S A, Stevens J G. Glycoprotein B is a specific determinant of herpes simplex virus type 1 neuroinvasiveness. Journal of Virology 1993; 67: 5948–5954
   PubMed Web of Science ®Google Scholar
• Zhu Z, Cai W, Schaffer P. Cooperativity among herpes simplex virus type 1 immediate early regulatory proteins: ICP4 and ICP27 affect the intracellular localization of ICP4. Journal of Virology 1994; 68: 3027–3040
   PubMed Web of Science ®Google Scholar