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Relating GPI-Anchored Ly6 Proteins uPAR and CD59 to Viral Infection

The Ly6 (lymphocyte antigen-6)/uPAR (urokinase-type plasminogen activator receptor) superfamily protein is a group of molecules that share limited sequence homology but conserved three-fingered structures. Despite diverse cellular functions, such as in regulating host immunity, cell adhesion, and mi...

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Detalles Bibliográficos
Autores principales: Yu, Jingyou, Murthy, Vaibhav, Liu, Shan-Lu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893729/
https://www.ncbi.nlm.nih.gov/pubmed/31739586
http://dx.doi.org/10.3390/v11111060
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author Yu, Jingyou
Murthy, Vaibhav
Liu, Shan-Lu
author_facet Yu, Jingyou
Murthy, Vaibhav
Liu, Shan-Lu
author_sort Yu, Jingyou
collection PubMed
description The Ly6 (lymphocyte antigen-6)/uPAR (urokinase-type plasminogen activator receptor) superfamily protein is a group of molecules that share limited sequence homology but conserved three-fingered structures. Despite diverse cellular functions, such as in regulating host immunity, cell adhesion, and migration, the physiological roles of these factors in vivo remain poorly characterized. Notably, increasing research has focused on the interplays between Ly6/uPAR proteins and viral pathogens, the results of which have provided new insight into viral entry and virus–host interactions. While LY6E (lymphocyte antigen 6 family member E), one key member of the Ly6E/uPAR-family proteins, has been extensively studied, other members have not been well characterized. Here, we summarize current knowledge of Ly6/uPAR proteins related to viral infection, with a focus on uPAR and CD59. Our goal is to provide an up-to-date view of the Ly6/uPAR-family proteins and associated virus–host interaction and viral pathogenesis.
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spelling pubmed-68937292019-12-23 Relating GPI-Anchored Ly6 Proteins uPAR and CD59 to Viral Infection Yu, Jingyou Murthy, Vaibhav Liu, Shan-Lu Viruses Review The Ly6 (lymphocyte antigen-6)/uPAR (urokinase-type plasminogen activator receptor) superfamily protein is a group of molecules that share limited sequence homology but conserved three-fingered structures. Despite diverse cellular functions, such as in regulating host immunity, cell adhesion, and migration, the physiological roles of these factors in vivo remain poorly characterized. Notably, increasing research has focused on the interplays between Ly6/uPAR proteins and viral pathogens, the results of which have provided new insight into viral entry and virus–host interactions. While LY6E (lymphocyte antigen 6 family member E), one key member of the Ly6E/uPAR-family proteins, has been extensively studied, other members have not been well characterized. Here, we summarize current knowledge of Ly6/uPAR proteins related to viral infection, with a focus on uPAR and CD59. Our goal is to provide an up-to-date view of the Ly6/uPAR-family proteins and associated virus–host interaction and viral pathogenesis. MDPI 2019-11-14 /pmc/articles/PMC6893729/ /pubmed/31739586 http://dx.doi.org/10.3390/v11111060 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Yu, Jingyou
Murthy, Vaibhav
Liu, Shan-Lu
Relating GPI-Anchored Ly6 Proteins uPAR and CD59 to Viral Infection
title Relating GPI-Anchored Ly6 Proteins uPAR and CD59 to Viral Infection
title_full Relating GPI-Anchored Ly6 Proteins uPAR and CD59 to Viral Infection
title_fullStr Relating GPI-Anchored Ly6 Proteins uPAR and CD59 to Viral Infection
title_full_unstemmed Relating GPI-Anchored Ly6 Proteins uPAR and CD59 to Viral Infection
title_short Relating GPI-Anchored Ly6 Proteins uPAR and CD59 to Viral Infection
title_sort relating gpi-anchored ly6 proteins upar and cd59 to viral infection
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893729/
https://www.ncbi.nlm.nih.gov/pubmed/31739586
http://dx.doi.org/10.3390/v11111060
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