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Enhancement of the antimycobacterial activity of macrophages by ajoene

Ajoene, a garlic-derived sulfur-containing compound, has broad-spectrum antimicrobial activity. To assess the potential of ajoene for treating tuberculosis (TB), we determined whether it induces the stress response of the endoplasmic reticulum (ER), which plays an important role in TB. We showed tha...

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Autores principales: Choi, Ji-Ae, Cho, Soo-Na, Lim, Yun-Ji, Lee, Junghwan, Go, Dam, Kim, Seon-Hwa, Song, Chang-Hwa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830758/
https://www.ncbi.nlm.nih.gov/pubmed/29239661
http://dx.doi.org/10.1177/1753425917747975
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author Choi, Ji-Ae
Cho, Soo-Na
Lim, Yun-Ji
Lee, Junghwan
Go, Dam
Kim, Seon-Hwa
Song, Chang-Hwa
author_facet Choi, Ji-Ae
Cho, Soo-Na
Lim, Yun-Ji
Lee, Junghwan
Go, Dam
Kim, Seon-Hwa
Song, Chang-Hwa
author_sort Choi, Ji-Ae
collection PubMed
description Ajoene, a garlic-derived sulfur-containing compound, has broad-spectrum antimicrobial activity. To assess the potential of ajoene for treating tuberculosis (TB), we determined whether it induces the stress response of the endoplasmic reticulum (ER), which plays an important role in TB. We showed that ajoene stimulation induced the production of ER stress sensor molecules and reactive oxygen species (ROS) levels. Ajoene-induced ROS production was dependent on c-Jun N-terminal kinase (JNK) activation. Interestingly, the inhibition of JNK activity and suppression of ROS production reduced ajoene-induced CHOP production in macrophages. Because ER stress activates autophagy, the activation of which suppresses the growth of mycobacteria, we investigated the ajoene-induced production of autophagy-related factors, including LC3-II, P62 and Beclin-1. As expected, ajoene treatment increased the levels of these factors in RAW 264.7 cells. Remarkably, the total amount of Mycobacterium tuberculosis (Mtb) H37Rv was significantly reduced in ajoene-treated RAW 264.7 cells. The treatment of macrophages with ajoene resulted in the activation of JNK, induction of ROS synthesis and accumulation of ROS, possibly leading to the activation of ER stress and autophagy. These results reveal the mechanism of the antimycobacterial effects of ajoene against Mtb H37Rv. Our findings might facilitate the development of novel therapies for patients with TB.
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spelling pubmed-68307582019-11-20 Enhancement of the antimycobacterial activity of macrophages by ajoene Choi, Ji-Ae Cho, Soo-Na Lim, Yun-Ji Lee, Junghwan Go, Dam Kim, Seon-Hwa Song, Chang-Hwa Innate Immun Original Articles Ajoene, a garlic-derived sulfur-containing compound, has broad-spectrum antimicrobial activity. To assess the potential of ajoene for treating tuberculosis (TB), we determined whether it induces the stress response of the endoplasmic reticulum (ER), which plays an important role in TB. We showed that ajoene stimulation induced the production of ER stress sensor molecules and reactive oxygen species (ROS) levels. Ajoene-induced ROS production was dependent on c-Jun N-terminal kinase (JNK) activation. Interestingly, the inhibition of JNK activity and suppression of ROS production reduced ajoene-induced CHOP production in macrophages. Because ER stress activates autophagy, the activation of which suppresses the growth of mycobacteria, we investigated the ajoene-induced production of autophagy-related factors, including LC3-II, P62 and Beclin-1. As expected, ajoene treatment increased the levels of these factors in RAW 264.7 cells. Remarkably, the total amount of Mycobacterium tuberculosis (Mtb) H37Rv was significantly reduced in ajoene-treated RAW 264.7 cells. The treatment of macrophages with ajoene resulted in the activation of JNK, induction of ROS synthesis and accumulation of ROS, possibly leading to the activation of ER stress and autophagy. These results reveal the mechanism of the antimycobacterial effects of ajoene against Mtb H37Rv. Our findings might facilitate the development of novel therapies for patients with TB. SAGE Publications 2017-12-14 2018-01 /pmc/articles/PMC6830758/ /pubmed/29239661 http://dx.doi.org/10.1177/1753425917747975 Text en © The Author(s) 2017 http://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Articles
Choi, Ji-Ae
Cho, Soo-Na
Lim, Yun-Ji
Lee, Junghwan
Go, Dam
Kim, Seon-Hwa
Song, Chang-Hwa
Enhancement of the antimycobacterial activity of macrophages by ajoene
title Enhancement of the antimycobacterial activity of macrophages by ajoene
title_full Enhancement of the antimycobacterial activity of macrophages by ajoene
title_fullStr Enhancement of the antimycobacterial activity of macrophages by ajoene
title_full_unstemmed Enhancement of the antimycobacterial activity of macrophages by ajoene
title_short Enhancement of the antimycobacterial activity of macrophages by ajoene
title_sort enhancement of the antimycobacterial activity of macrophages by ajoene
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6830758/
https://www.ncbi.nlm.nih.gov/pubmed/29239661
http://dx.doi.org/10.1177/1753425917747975
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