Utilization of human DC-SIGN and L-SIGN for entry and infection of host cells by the New World arenavirus, Junín virus

The target cell tropism of enveloped viruses is regulated by interactions between viral proteins and cellular receptors determining susceptibility at a host cell, tissue or species level. However, a number of additional cell-surface moieties can also bind viral envelope glycoproteins and could act a...

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Autores principales: Martínez, María Guadalupe, Cordo, Sandra M., Candurra, Nélida Alicia
Publicado: 2013
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0006291X_v441_n3_p612_Martinez
http://hdl.handle.net/20.500.12110/paper_0006291X_v441_n3_p612_Martinez
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spelling paper:paper_0006291X_v441_n3_p612_Martinez2023-06-08T14:30:21Z Utilization of human DC-SIGN and L-SIGN for entry and infection of host cells by the New World arenavirus, Junín virus Martínez, María Guadalupe Cordo, Sandra M. Candurra, Nélida Alicia Junín arenavirus Lectin Virus entry Virus receptor CD209 antigen lectin membrane protein protein l sign unclassified drug article cell surface comparative study controlled study host cell human internalization Junin virus Murine leukemia virus nonhuman priority journal Vesicular stomatitis virus virus culture virus entry virus envelope virus infection virus infectivity virus particle Arenavirus Junin virus Junín arenavirus Lectin Virus entry Virus receptor 3T3 Cells Animals Antigens, CD Cell Adhesion Molecules Cercopithecus aethiops Hemorrhagic Fever, American Host-Pathogen Interactions Humans Junin virus Lectins, C-Type Membrane Glycoproteins Mice Receptors, Cell Surface Receptors, Transferrin Vero Cells Viral Envelope Proteins Virus Internalization The target cell tropism of enveloped viruses is regulated by interactions between viral proteins and cellular receptors determining susceptibility at a host cell, tissue or species level. However, a number of additional cell-surface moieties can also bind viral envelope glycoproteins and could act as capture receptors, serving as attachment factors to concentrate virus particles on the cell surface, or to disseminate the virus infection to target organs or susceptible cells within the host. Here, we used Junín virus (JUNV) or JUNV glycoprotein complex (GPC)-pseudotyped particles to study their ability to be internalized by the human C-type lectins hDC- or hL-SIGN. Our results provide evidence that hDC- and hL-SIGN can mediate the entry of Junín virus into cells, and may play an important role in virus infection and dissemination in the host. © 2013 Elsevier Inc. Fil:Martinez, M.G. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Cordo, S.M. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. Fil:Candurra, N.A. Universidad de Buenos Aires. Facultad de Ciencias Exactas y Naturales; Argentina. 2013 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0006291X_v441_n3_p612_Martinez http://hdl.handle.net/20.500.12110/paper_0006291X_v441_n3_p612_Martinez
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Junín arenavirus
Lectin
Virus entry
Virus receptor
CD209 antigen
lectin
membrane protein
protein l sign
unclassified drug
article
cell surface
comparative study
controlled study
host cell
human
internalization
Junin virus
Murine leukemia virus
nonhuman
priority journal
Vesicular stomatitis virus
virus culture
virus entry
virus envelope
virus infection
virus infectivity
virus particle
Arenavirus
Junin virus
Junín arenavirus
Lectin
Virus entry
Virus receptor
3T3 Cells
Animals
Antigens, CD
Cell Adhesion Molecules
Cercopithecus aethiops
Hemorrhagic Fever, American
Host-Pathogen Interactions
Humans
Junin virus
Lectins, C-Type
Membrane Glycoproteins
Mice
Receptors, Cell Surface
Receptors, Transferrin
Vero Cells
Viral Envelope Proteins
Virus Internalization
spellingShingle Junín arenavirus
Lectin
Virus entry
Virus receptor
CD209 antigen
lectin
membrane protein
protein l sign
unclassified drug
article
cell surface
comparative study
controlled study
host cell
human
internalization
Junin virus
Murine leukemia virus
nonhuman
priority journal
Vesicular stomatitis virus
virus culture
virus entry
virus envelope
virus infection
virus infectivity
virus particle
Arenavirus
Junin virus
Junín arenavirus
Lectin
Virus entry
Virus receptor
3T3 Cells
Animals
Antigens, CD
Cell Adhesion Molecules
Cercopithecus aethiops
Hemorrhagic Fever, American
Host-Pathogen Interactions
Humans
Junin virus
Lectins, C-Type
Membrane Glycoproteins
Mice
Receptors, Cell Surface
Receptors, Transferrin
Vero Cells
Viral Envelope Proteins
Virus Internalization
Martínez, María Guadalupe
Cordo, Sandra M.
Candurra, Nélida Alicia
Utilization of human DC-SIGN and L-SIGN for entry and infection of host cells by the New World arenavirus, Junín virus
topic_facet Junín arenavirus
Lectin
Virus entry
Virus receptor
CD209 antigen
lectin
membrane protein
protein l sign
unclassified drug
article
cell surface
comparative study
controlled study
host cell
human
internalization
Junin virus
Murine leukemia virus
nonhuman
priority journal
Vesicular stomatitis virus
virus culture
virus entry
virus envelope
virus infection
virus infectivity
virus particle
Arenavirus
Junin virus
Junín arenavirus
Lectin
Virus entry
Virus receptor
3T3 Cells
Animals
Antigens, CD
Cell Adhesion Molecules
Cercopithecus aethiops
Hemorrhagic Fever, American
Host-Pathogen Interactions
Humans
Junin virus
Lectins, C-Type
Membrane Glycoproteins
Mice
Receptors, Cell Surface
Receptors, Transferrin
Vero Cells
Viral Envelope Proteins
Virus Internalization
description The target cell tropism of enveloped viruses is regulated by interactions between viral proteins and cellular receptors determining susceptibility at a host cell, tissue or species level. However, a number of additional cell-surface moieties can also bind viral envelope glycoproteins and could act as capture receptors, serving as attachment factors to concentrate virus particles on the cell surface, or to disseminate the virus infection to target organs or susceptible cells within the host. Here, we used Junín virus (JUNV) or JUNV glycoprotein complex (GPC)-pseudotyped particles to study their ability to be internalized by the human C-type lectins hDC- or hL-SIGN. Our results provide evidence that hDC- and hL-SIGN can mediate the entry of Junín virus into cells, and may play an important role in virus infection and dissemination in the host. © 2013 Elsevier Inc.
author Martínez, María Guadalupe
Cordo, Sandra M.
Candurra, Nélida Alicia
author_facet Martínez, María Guadalupe
Cordo, Sandra M.
Candurra, Nélida Alicia
author_sort Martínez, María Guadalupe
title Utilization of human DC-SIGN and L-SIGN for entry and infection of host cells by the New World arenavirus, Junín virus
title_short Utilization of human DC-SIGN and L-SIGN for entry and infection of host cells by the New World arenavirus, Junín virus
title_full Utilization of human DC-SIGN and L-SIGN for entry and infection of host cells by the New World arenavirus, Junín virus
title_fullStr Utilization of human DC-SIGN and L-SIGN for entry and infection of host cells by the New World arenavirus, Junín virus
title_full_unstemmed Utilization of human DC-SIGN and L-SIGN for entry and infection of host cells by the New World arenavirus, Junín virus
title_sort utilization of human dc-sign and l-sign for entry and infection of host cells by the new world arenavirus, junín virus
publishDate 2013
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_0006291X_v441_n3_p612_Martinez
http://hdl.handle.net/20.500.12110/paper_0006291X_v441_n3_p612_Martinez
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AT cordosandram utilizationofhumandcsignandlsignforentryandinfectionofhostcellsbythenewworldarenavirusjuninvirus
AT candurranelidaalicia utilizationofhumandcsignandlsignforentryandinfectionofhostcellsbythenewworldarenavirusjuninvirus
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