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Response of human macrophages to gamma radiation is mediated via expression of endogenous retroviruses

Ionizing radiation-induced tissue damage recruits monocytes into the exposed area where they are differentiated to macrophages. These implement phagocytic removal of dying cells and elicit an acute inflammatory response, but can also facilitate tumorigenesis due to production of anti-inflammatory cy...

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Autores principales: Mikhalkevich, Natallia, O’Carroll, Ina P., Tkavc, Rok, Lund, Kateryna, Sukumar, Gauthaman, Dalgard, Clifton L., Johnson, Kory R., Li, Wenxue, Wang, Tongguang, Nath, Avindra, Iordanskiy, Sergey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895352/
https://www.ncbi.nlm.nih.gov/pubmed/33556144
http://dx.doi.org/10.1371/journal.ppat.1009305
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author Mikhalkevich, Natallia
O’Carroll, Ina P.
Tkavc, Rok
Lund, Kateryna
Sukumar, Gauthaman
Dalgard, Clifton L.
Johnson, Kory R.
Li, Wenxue
Wang, Tongguang
Nath, Avindra
Iordanskiy, Sergey
author_facet Mikhalkevich, Natallia
O’Carroll, Ina P.
Tkavc, Rok
Lund, Kateryna
Sukumar, Gauthaman
Dalgard, Clifton L.
Johnson, Kory R.
Li, Wenxue
Wang, Tongguang
Nath, Avindra
Iordanskiy, Sergey
author_sort Mikhalkevich, Natallia
collection PubMed
description Ionizing radiation-induced tissue damage recruits monocytes into the exposed area where they are differentiated to macrophages. These implement phagocytic removal of dying cells and elicit an acute inflammatory response, but can also facilitate tumorigenesis due to production of anti-inflammatory cytokines. Using primary human monocyte-derived macrophages (MDMs) and the THP1 monocytic cell line, we demonstrate that gamma radiation triggers monocyte differentiation toward the macrophage phenotype with increased expression of type I interferons (IFN-I) and both pro- and anti-inflammatory macrophage activation markers. We found that these changes correlate with significantly upregulated expression of 622 retroelements from various groups, particularly of several clades of human endogenous retroviruses (HERVs). Elevated transcription was detected in both sense and antisense directions in the HERV subgroups tested, including the most genetically homogeneous clade HML-2. The level of antisense transcription was three- to five-fold higher than of the sense strand levels. Using a proximity ligation assay and immunoprecipitation followed by RNA quantification, we identified an increased amount of the dsRNA receptors MDA-5 and TLR3 bound to an equivalent number of copies of sense and antisense chains of HERVK HML-2 RNA. This binding triggered MAVS-associated signaling pathways resulting in increased expression of IFN-I and inflammation related genes that enhanced the cumulative inflammatory effect of radiation-induced senescence. HML-2 knockdown was accompanied with reduced expression and secretion of IFNα, pro-inflammatory (IL-1β, IL-6, CCL2, CCL3, CCL8, and CCL20) and anti-inflammatory (IL10) modulators in irradiated monocytes and MDMs. Taken together, our data indicate that radiation stress-induced HERV expression enhances the IFN-I and cytokine response and results in increased levels of pro-inflammatory modulators along with expression of anti-inflammatory factors associated with the macrophage tumorigenic phenotype.
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spelling pubmed-78953522021-03-01 Response of human macrophages to gamma radiation is mediated via expression of endogenous retroviruses Mikhalkevich, Natallia O’Carroll, Ina P. Tkavc, Rok Lund, Kateryna Sukumar, Gauthaman Dalgard, Clifton L. Johnson, Kory R. Li, Wenxue Wang, Tongguang Nath, Avindra Iordanskiy, Sergey PLoS Pathog Research Article Ionizing radiation-induced tissue damage recruits monocytes into the exposed area where they are differentiated to macrophages. These implement phagocytic removal of dying cells and elicit an acute inflammatory response, but can also facilitate tumorigenesis due to production of anti-inflammatory cytokines. Using primary human monocyte-derived macrophages (MDMs) and the THP1 monocytic cell line, we demonstrate that gamma radiation triggers monocyte differentiation toward the macrophage phenotype with increased expression of type I interferons (IFN-I) and both pro- and anti-inflammatory macrophage activation markers. We found that these changes correlate with significantly upregulated expression of 622 retroelements from various groups, particularly of several clades of human endogenous retroviruses (HERVs). Elevated transcription was detected in both sense and antisense directions in the HERV subgroups tested, including the most genetically homogeneous clade HML-2. The level of antisense transcription was three- to five-fold higher than of the sense strand levels. Using a proximity ligation assay and immunoprecipitation followed by RNA quantification, we identified an increased amount of the dsRNA receptors MDA-5 and TLR3 bound to an equivalent number of copies of sense and antisense chains of HERVK HML-2 RNA. This binding triggered MAVS-associated signaling pathways resulting in increased expression of IFN-I and inflammation related genes that enhanced the cumulative inflammatory effect of radiation-induced senescence. HML-2 knockdown was accompanied with reduced expression and secretion of IFNα, pro-inflammatory (IL-1β, IL-6, CCL2, CCL3, CCL8, and CCL20) and anti-inflammatory (IL10) modulators in irradiated monocytes and MDMs. Taken together, our data indicate that radiation stress-induced HERV expression enhances the IFN-I and cytokine response and results in increased levels of pro-inflammatory modulators along with expression of anti-inflammatory factors associated with the macrophage tumorigenic phenotype. Public Library of Science 2021-02-08 /pmc/articles/PMC7895352/ /pubmed/33556144 http://dx.doi.org/10.1371/journal.ppat.1009305 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
spellingShingle Research Article
Mikhalkevich, Natallia
O’Carroll, Ina P.
Tkavc, Rok
Lund, Kateryna
Sukumar, Gauthaman
Dalgard, Clifton L.
Johnson, Kory R.
Li, Wenxue
Wang, Tongguang
Nath, Avindra
Iordanskiy, Sergey
Response of human macrophages to gamma radiation is mediated via expression of endogenous retroviruses
title Response of human macrophages to gamma radiation is mediated via expression of endogenous retroviruses
title_full Response of human macrophages to gamma radiation is mediated via expression of endogenous retroviruses
title_fullStr Response of human macrophages to gamma radiation is mediated via expression of endogenous retroviruses
title_full_unstemmed Response of human macrophages to gamma radiation is mediated via expression of endogenous retroviruses
title_short Response of human macrophages to gamma radiation is mediated via expression of endogenous retroviruses
title_sort response of human macrophages to gamma radiation is mediated via expression of endogenous retroviruses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895352/
https://www.ncbi.nlm.nih.gov/pubmed/33556144
http://dx.doi.org/10.1371/journal.ppat.1009305
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