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Chloromethylisothiazolinone induces ER stress-induced stress granule formation in human keratinocytes

Chloromethylisothiazolinone (CMIT), a humidifier disinfectant, is known to be toxic to the respiratory system. While the toxic effect of CMIT on the lungs has been widely investigated, its effect on the skin is well unknown. In this study, we examined stress granule (SG) formation to investigate the...

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Autores principales: Jung, Da-Min, Kim, Kee K., Kim, Eun-Mi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448836/
https://www.ncbi.nlm.nih.gov/pubmed/37636324
http://dx.doi.org/10.1080/19768354.2023.2250852
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author Jung, Da-Min
Kim, Kee K.
Kim, Eun-Mi
author_facet Jung, Da-Min
Kim, Kee K.
Kim, Eun-Mi
author_sort Jung, Da-Min
collection PubMed
description Chloromethylisothiazolinone (CMIT), a humidifier disinfectant, is known to be toxic to the respiratory system. While the toxic effect of CMIT on the lungs has been widely investigated, its effect on the skin is well unknown. In this study, we examined stress granule (SG) formation to investigate the cytotoxic effects of CMIT on human keratinocytes. We assessed the viability of the cells following CMIT exposure and performed immunofluorescence microscopy and immunoblot analyses to determine SG formation and downstream pathways. The IC(50) values in human keratinocyte HaCaT cells after CMIT exposure for 1 and 24 h were 11 and 8 μg/mL, respectively, showing no significant difference. As determined using immunofluorescence microscopy, SG formation was effectively induced after CMIT exposure. Moreover, the phosphorylation of eukaryotic initiation factor-2α (eIF2α), a translation initiation factor, and protein kinase R-like endoplasmic reticulum (ER) kinase, which plays a role in the ER stress-mediated eIF2α phosphorylation, was confirmed by CMIT exposure. These results suggest that exposure to CMIT can have detrimental effects on the skin, even briefly, by inducing SG formation through ER stress in keratinocytes.
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spelling pubmed-104488362023-08-25 Chloromethylisothiazolinone induces ER stress-induced stress granule formation in human keratinocytes Jung, Da-Min Kim, Kee K. Kim, Eun-Mi Anim Cells Syst (Seoul) Research Article Chloromethylisothiazolinone (CMIT), a humidifier disinfectant, is known to be toxic to the respiratory system. While the toxic effect of CMIT on the lungs has been widely investigated, its effect on the skin is well unknown. In this study, we examined stress granule (SG) formation to investigate the cytotoxic effects of CMIT on human keratinocytes. We assessed the viability of the cells following CMIT exposure and performed immunofluorescence microscopy and immunoblot analyses to determine SG formation and downstream pathways. The IC(50) values in human keratinocyte HaCaT cells after CMIT exposure for 1 and 24 h were 11 and 8 μg/mL, respectively, showing no significant difference. As determined using immunofluorescence microscopy, SG formation was effectively induced after CMIT exposure. Moreover, the phosphorylation of eukaryotic initiation factor-2α (eIF2α), a translation initiation factor, and protein kinase R-like endoplasmic reticulum (ER) kinase, which plays a role in the ER stress-mediated eIF2α phosphorylation, was confirmed by CMIT exposure. These results suggest that exposure to CMIT can have detrimental effects on the skin, even briefly, by inducing SG formation through ER stress in keratinocytes. Taylor & Francis 2023-08-23 /pmc/articles/PMC10448836/ /pubmed/37636324 http://dx.doi.org/10.1080/19768354.2023.2250852 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent.
spellingShingle Research Article
Jung, Da-Min
Kim, Kee K.
Kim, Eun-Mi
Chloromethylisothiazolinone induces ER stress-induced stress granule formation in human keratinocytes
title Chloromethylisothiazolinone induces ER stress-induced stress granule formation in human keratinocytes
title_full Chloromethylisothiazolinone induces ER stress-induced stress granule formation in human keratinocytes
title_fullStr Chloromethylisothiazolinone induces ER stress-induced stress granule formation in human keratinocytes
title_full_unstemmed Chloromethylisothiazolinone induces ER stress-induced stress granule formation in human keratinocytes
title_short Chloromethylisothiazolinone induces ER stress-induced stress granule formation in human keratinocytes
title_sort chloromethylisothiazolinone induces er stress-induced stress granule formation in human keratinocytes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10448836/
https://www.ncbi.nlm.nih.gov/pubmed/37636324
http://dx.doi.org/10.1080/19768354.2023.2250852
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