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US28: HCMV’s Swiss Army Knife

US28 is one of four G protein coupled receptors (GPCRs) encoded by human cytomegalovirus (HCMV). The US28 protein (pUS28) is a potent signaling molecule that alters a variety of cellular pathways that ultimately alter the host cell environment. This viral GPCR is expressed not only in the context of...

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Detalles Bibliográficos
Autores principales: Krishna, Benjamin A., Miller, William E., O’Connor, Christine M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116241/
https://www.ncbi.nlm.nih.gov/pubmed/30127279
http://dx.doi.org/10.3390/v10080445
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author Krishna, Benjamin A.
Miller, William E.
O’Connor, Christine M.
author_facet Krishna, Benjamin A.
Miller, William E.
O’Connor, Christine M.
author_sort Krishna, Benjamin A.
collection PubMed
description US28 is one of four G protein coupled receptors (GPCRs) encoded by human cytomegalovirus (HCMV). The US28 protein (pUS28) is a potent signaling molecule that alters a variety of cellular pathways that ultimately alter the host cell environment. This viral GPCR is expressed not only in the context of lytic replication but also during viral latency, highlighting its multifunctional properties. pUS28 is a functional GPCR, and its manipulation of multiple signaling pathways likely impacts HCMV pathogenesis. Herein, we will discuss the impact of pUS28 on both lytic and latent infection, pUS28-mediated signaling and its downstream consequences, and the influence this viral GPCR may have on disease states, including cardiovascular disease and cancer. We will also discuss the potential for and progress towards exploiting pUS28 as a novel therapeutic to combat HCMV.
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spelling pubmed-61162412018-08-31 US28: HCMV’s Swiss Army Knife Krishna, Benjamin A. Miller, William E. O’Connor, Christine M. Viruses Review US28 is one of four G protein coupled receptors (GPCRs) encoded by human cytomegalovirus (HCMV). The US28 protein (pUS28) is a potent signaling molecule that alters a variety of cellular pathways that ultimately alter the host cell environment. This viral GPCR is expressed not only in the context of lytic replication but also during viral latency, highlighting its multifunctional properties. pUS28 is a functional GPCR, and its manipulation of multiple signaling pathways likely impacts HCMV pathogenesis. Herein, we will discuss the impact of pUS28 on both lytic and latent infection, pUS28-mediated signaling and its downstream consequences, and the influence this viral GPCR may have on disease states, including cardiovascular disease and cancer. We will also discuss the potential for and progress towards exploiting pUS28 as a novel therapeutic to combat HCMV. MDPI 2018-08-20 /pmc/articles/PMC6116241/ /pubmed/30127279 http://dx.doi.org/10.3390/v10080445 Text en © 2018 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
Krishna, Benjamin A.
Miller, William E.
O’Connor, Christine M.
US28: HCMV’s Swiss Army Knife
title US28: HCMV’s Swiss Army Knife
title_full US28: HCMV’s Swiss Army Knife
title_fullStr US28: HCMV’s Swiss Army Knife
title_full_unstemmed US28: HCMV’s Swiss Army Knife
title_short US28: HCMV’s Swiss Army Knife
title_sort us28: hcmv’s swiss army knife
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6116241/
https://www.ncbi.nlm.nih.gov/pubmed/30127279
http://dx.doi.org/10.3390/v10080445
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