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The Bacterial Product Violacein Exerts an Immunostimulatory Effect Via TLR8

Violacein, an indole-derived, purple-colored natural pigment isolated from Chromobacterium violaceum has shown multiple biological activities. In this work, we studied the effect of violacein in different immune cell lines, namely THP-1, MonoMac 6, ANA-1, Raw 264.7 cells, as well as in human periphe...

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Autores principales: Venegas, Francisco A., Köllisch, Gabriele, Mark, Kerstin, Diederich, Wibke E., Kaufmann, Andreas, Bauer, Stefan, Chavarría, Max, Araya, Juan J., García-Piñeres, Alfonso J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754391/
https://www.ncbi.nlm.nih.gov/pubmed/31541142
http://dx.doi.org/10.1038/s41598-019-50038-x
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author Venegas, Francisco A.
Köllisch, Gabriele
Mark, Kerstin
Diederich, Wibke E.
Kaufmann, Andreas
Bauer, Stefan
Chavarría, Max
Araya, Juan J.
García-Piñeres, Alfonso J.
author_facet Venegas, Francisco A.
Köllisch, Gabriele
Mark, Kerstin
Diederich, Wibke E.
Kaufmann, Andreas
Bauer, Stefan
Chavarría, Max
Araya, Juan J.
García-Piñeres, Alfonso J.
author_sort Venegas, Francisco A.
collection PubMed
description Violacein, an indole-derived, purple-colored natural pigment isolated from Chromobacterium violaceum has shown multiple biological activities. In this work, we studied the effect of violacein in different immune cell lines, namely THP-1, MonoMac 6, ANA-1, Raw 264.7 cells, as well as in human peripheral blood mononuclear cells (PBMCs). A stimulation of TNF-α production was observed in murine macrophages (ANA-1 and Raw 264.7), and in PBMCs, IL-6 and IL-1β secretion was detected. We obtained evidence of the molecular mechanism of activation by determining the mRNA expression pattern upon treatment with violacein in Raw 264.7 cells. Incubation with violacein caused activation of pathways related with an immune and inflammatory response. Our data utilizing TLR-transfected HEK-293 cells indicate that violacein activates the human TLR8 (hTLR8) receptor signaling pathway and not human TLR7 (hTLR7). Furthermore, we found that the immunostimulatory effect of violacein in PBMCs could be suppressed by the specific hTLR8 antagonist, CU-CPT9a. Finally, we studied the interaction of hTLR8 with violacein in silico and obtained evidence that violacein could bind to hTLR8 in a similar fashion to imidazoquinoline compounds. Therefore, our results indicate that violacein may have some potential in contributing to future immune therapy strategies.
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spelling pubmed-67543912019-10-02 The Bacterial Product Violacein Exerts an Immunostimulatory Effect Via TLR8 Venegas, Francisco A. Köllisch, Gabriele Mark, Kerstin Diederich, Wibke E. Kaufmann, Andreas Bauer, Stefan Chavarría, Max Araya, Juan J. García-Piñeres, Alfonso J. Sci Rep Article Violacein, an indole-derived, purple-colored natural pigment isolated from Chromobacterium violaceum has shown multiple biological activities. In this work, we studied the effect of violacein in different immune cell lines, namely THP-1, MonoMac 6, ANA-1, Raw 264.7 cells, as well as in human peripheral blood mononuclear cells (PBMCs). A stimulation of TNF-α production was observed in murine macrophages (ANA-1 and Raw 264.7), and in PBMCs, IL-6 and IL-1β secretion was detected. We obtained evidence of the molecular mechanism of activation by determining the mRNA expression pattern upon treatment with violacein in Raw 264.7 cells. Incubation with violacein caused activation of pathways related with an immune and inflammatory response. Our data utilizing TLR-transfected HEK-293 cells indicate that violacein activates the human TLR8 (hTLR8) receptor signaling pathway and not human TLR7 (hTLR7). Furthermore, we found that the immunostimulatory effect of violacein in PBMCs could be suppressed by the specific hTLR8 antagonist, CU-CPT9a. Finally, we studied the interaction of hTLR8 with violacein in silico and obtained evidence that violacein could bind to hTLR8 in a similar fashion to imidazoquinoline compounds. Therefore, our results indicate that violacein may have some potential in contributing to future immune therapy strategies. Nature Publishing Group UK 2019-09-20 /pmc/articles/PMC6754391/ /pubmed/31541142 http://dx.doi.org/10.1038/s41598-019-50038-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Venegas, Francisco A.
Köllisch, Gabriele
Mark, Kerstin
Diederich, Wibke E.
Kaufmann, Andreas
Bauer, Stefan
Chavarría, Max
Araya, Juan J.
García-Piñeres, Alfonso J.
The Bacterial Product Violacein Exerts an Immunostimulatory Effect Via TLR8
title The Bacterial Product Violacein Exerts an Immunostimulatory Effect Via TLR8
title_full The Bacterial Product Violacein Exerts an Immunostimulatory Effect Via TLR8
title_fullStr The Bacterial Product Violacein Exerts an Immunostimulatory Effect Via TLR8
title_full_unstemmed The Bacterial Product Violacein Exerts an Immunostimulatory Effect Via TLR8
title_short The Bacterial Product Violacein Exerts an Immunostimulatory Effect Via TLR8
title_sort bacterial product violacein exerts an immunostimulatory effect via tlr8
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6754391/
https://www.ncbi.nlm.nih.gov/pubmed/31541142
http://dx.doi.org/10.1038/s41598-019-50038-x
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