Nectin-1/HveC mediates herpes simplex virus type 1 entry into primary human sensory neurons and fibroblasts

被引:0
作者
Scott A. Simpson
Michael D. Manchak
Elizabeth J. Hager
Claude Krummenacher
J. Charles Whitbeck
Myron J. Levin
Curt R. Freed
Christine L. Wilcox
Gary H. Cohen
Roselyn J. Eisenberg
Lewis I. Pizer
机构
[1] University of Colorado Health Sciences Center,Department of Pediatrics, Section of Infectious Diseases
[2] University of Pennsylvania,Department of Microbiology
[3] University of Pennsylvania,Center for Oral Health Research, School of Dental Medicine
[4] University of Colorado Health Sciences Center,Department of Medicine, Division of Clinical Pharmacology
[5] Colorado State University,Department of Microbiology
[6] University of Pennsylvania,Department of Pathobiology, School of Veterinary Medicine
[7] University of Colorado Health Sciences Center,Program of Molecular Biology and Department of Microbiology
[8] University of Colorado Health Sciences Center,Department of Microbiology
来源
Journal of NeuroVirology | 2005年 / 11卷
关键词
HSV-1; human neurons; receptors;
D O I
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中图分类号
学科分类号
摘要
Immunocytochemistry detects nectin-1/HveC, nectin-2/HveB, and HVEM/HveA on the surface of sensory neurons and fibroblasts grown as primary cultures from human dorsal root ganglia. Viral entry into these cultured cells was assayed by infection with a recombinant herpes simplex virus type 1 (HSV-1) expressing green fluorescent protein. Soluble, truncated nectin-1 polypeptide, as well as polyclonal and monoclonal antibodies against nectin-1, inhibited infection of neurons, whereas polypeptides and antibodies capable of inhibiting HSV-1 interaction with nectin-2 and herpesvirus entry mediator (HVEM) failed to prevent infection of neuronal cells. These results demonstrate that nectin-1 is the primary receptor for HSV-1 entry into human fetal neurons. Viral entry into fibroblasts was also reduced by soluble nectin-1 but not by soluble HVEM. However, in contrast to the results obtained with neurons, antibodies against receptors failed to inhibit entry into fibroblasts, indicating that unlike neurons, fibroblasts have multiple receptors or mechanisms for HSV-1 entry.
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页码:208 / 218
页数:10
相关论文
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