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Deoxyguanosine is a TLR7 agonist

Toll‐like receptor 7 (TLR7) is an innate immune sensor for single‐strand RNA (ssRNA). Recent structural analysis revealed that TLR7 has an additional binding site for nucleosides such as guanosine, and is activated when both guanosine and ssRNA bind. The nucleoside binding site also accommodates imi...

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Autores principales: Davenne, Tamara, Bridgeman, Anne, Rigby, Rachel E., Rehwinkel, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972671/
https://www.ncbi.nlm.nih.gov/pubmed/31608988
http://dx.doi.org/10.1002/eji.201948151
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author Davenne, Tamara
Bridgeman, Anne
Rigby, Rachel E.
Rehwinkel, Jan
author_facet Davenne, Tamara
Bridgeman, Anne
Rigby, Rachel E.
Rehwinkel, Jan
author_sort Davenne, Tamara
collection PubMed
description Toll‐like receptor 7 (TLR7) is an innate immune sensor for single‐strand RNA (ssRNA). Recent structural analysis revealed that TLR7 has an additional binding site for nucleosides such as guanosine, and is activated when both guanosine and ssRNA bind. The nucleoside binding site also accommodates imidazoquinoline derivatives such as R848, which activate TLR7 in the absence of ssRNA. Here, we report that deoxyguanosine (dG) triggered cytokine production in murine bone marrow derived macrophages and plasmacytoid dendritic cells, as well as in human peripheral blood mononuclear cells, including type I interferons and pro‐inflammatory factors such as TNF and IL‐6. This signalling activity of dG was dependent on TLR7 and its adaptor MyD88 and did not require amplification via the type I interferon receptor. dG‐triggered cytokine production required endosomal maturation but did not depend on the concurrent provision of RNA. We conclude that dG induces an inflammatory response through TLR7 and propose that dG is an RNA‐independent TLR7 agonist.
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spelling pubmed-69726712020-01-27 Deoxyguanosine is a TLR7 agonist Davenne, Tamara Bridgeman, Anne Rigby, Rachel E. Rehwinkel, Jan Eur J Immunol Innate immunity Toll‐like receptor 7 (TLR7) is an innate immune sensor for single‐strand RNA (ssRNA). Recent structural analysis revealed that TLR7 has an additional binding site for nucleosides such as guanosine, and is activated when both guanosine and ssRNA bind. The nucleoside binding site also accommodates imidazoquinoline derivatives such as R848, which activate TLR7 in the absence of ssRNA. Here, we report that deoxyguanosine (dG) triggered cytokine production in murine bone marrow derived macrophages and plasmacytoid dendritic cells, as well as in human peripheral blood mononuclear cells, including type I interferons and pro‐inflammatory factors such as TNF and IL‐6. This signalling activity of dG was dependent on TLR7 and its adaptor MyD88 and did not require amplification via the type I interferon receptor. dG‐triggered cytokine production required endosomal maturation but did not depend on the concurrent provision of RNA. We conclude that dG induces an inflammatory response through TLR7 and propose that dG is an RNA‐independent TLR7 agonist. John Wiley and Sons Inc. 2019-11-14 2020-01 /pmc/articles/PMC6972671/ /pubmed/31608988 http://dx.doi.org/10.1002/eji.201948151 Text en © 2019 The Authors. European Journal of Immunology published by WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Innate immunity
Davenne, Tamara
Bridgeman, Anne
Rigby, Rachel E.
Rehwinkel, Jan
Deoxyguanosine is a TLR7 agonist
title Deoxyguanosine is a TLR7 agonist
title_full Deoxyguanosine is a TLR7 agonist
title_fullStr Deoxyguanosine is a TLR7 agonist
title_full_unstemmed Deoxyguanosine is a TLR7 agonist
title_short Deoxyguanosine is a TLR7 agonist
title_sort deoxyguanosine is a tlr7 agonist
topic Innate immunity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6972671/
https://www.ncbi.nlm.nih.gov/pubmed/31608988
http://dx.doi.org/10.1002/eji.201948151
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