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Human cytomegalovirus replication induces endothelial cell interleukin-11
Endothelial cells (EC) are critical sites of human cytomegalovirus (hCMV) infection in vivo. Infection can induce the production of various EC cytokines, such as interleukin (IL-)6, which can have autocrine and/or paracrine effector functions. Here, we report that hCMV induces the production of EC I...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Science Ltd
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299253/ https://www.ncbi.nlm.nih.gov/pubmed/29807687 http://dx.doi.org/10.1016/j.cyto.2018.05.018 |
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author | Gustafsson, K.L.R. Renné, T. Söderberg-Naucler, C. Butler, L.M. |
author_facet | Gustafsson, K.L.R. Renné, T. Söderberg-Naucler, C. Butler, L.M. |
author_sort | Gustafsson, K.L.R. |
collection | PubMed |
description | Endothelial cells (EC) are critical sites of human cytomegalovirus (hCMV) infection in vivo. Infection can induce the production of various EC cytokines, such as interleukin (IL-)6, which can have autocrine and/or paracrine effector functions. Here, we report that hCMV induces the production of EC IL-11, a relatively understudied member of the IL-6-type cytokine family. We detail temporal EC IL-11 translation and protein secretion dynamics in response to hCMV infection, and reveal distinct differences compared to EC IL-6. Viral replication had markedly opposing effects on the regulation of these closely related cytokines, representing a major driving force behind IL-11 production, whilst concurrently suppressing IL-6 expression. This is the first report of any biological agent that stimulates EC IL-11 production. |
format | Online Article Text |
id | pubmed-6299253 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Elsevier Science Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-62992532018-12-21 Human cytomegalovirus replication induces endothelial cell interleukin-11 Gustafsson, K.L.R. Renné, T. Söderberg-Naucler, C. Butler, L.M. Cytokine Article Endothelial cells (EC) are critical sites of human cytomegalovirus (hCMV) infection in vivo. Infection can induce the production of various EC cytokines, such as interleukin (IL-)6, which can have autocrine and/or paracrine effector functions. Here, we report that hCMV induces the production of EC IL-11, a relatively understudied member of the IL-6-type cytokine family. We detail temporal EC IL-11 translation and protein secretion dynamics in response to hCMV infection, and reveal distinct differences compared to EC IL-6. Viral replication had markedly opposing effects on the regulation of these closely related cytokines, representing a major driving force behind IL-11 production, whilst concurrently suppressing IL-6 expression. This is the first report of any biological agent that stimulates EC IL-11 production. Elsevier Science Ltd 2018-11 /pmc/articles/PMC6299253/ /pubmed/29807687 http://dx.doi.org/10.1016/j.cyto.2018.05.018 Text en © 2018 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Gustafsson, K.L.R. Renné, T. Söderberg-Naucler, C. Butler, L.M. Human cytomegalovirus replication induces endothelial cell interleukin-11 |
title | Human cytomegalovirus replication induces endothelial cell interleukin-11 |
title_full | Human cytomegalovirus replication induces endothelial cell interleukin-11 |
title_fullStr | Human cytomegalovirus replication induces endothelial cell interleukin-11 |
title_full_unstemmed | Human cytomegalovirus replication induces endothelial cell interleukin-11 |
title_short | Human cytomegalovirus replication induces endothelial cell interleukin-11 |
title_sort | human cytomegalovirus replication induces endothelial cell interleukin-11 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6299253/ https://www.ncbi.nlm.nih.gov/pubmed/29807687 http://dx.doi.org/10.1016/j.cyto.2018.05.018 |
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