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

      research-article
      a , a , b
      Animal Cells and Systems
      Taylor & Francis
      Chloromethylisothiazolinone, Keratinocyte, Protein kinase R-like endoplasmic reticulum kinase, Endoplasmic reticulum-stress, Stress granule

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          ABSTRACT

          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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          Most cited references33

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          ER-stress-induced transcriptional regulation increases protein synthesis leading to cell death.

          Protein misfolding in the endoplasmic reticulum (ER) leads to cell death through PERK-mediated phosphorylation of eIF2α, although the mechanism is not understood. ChIP-seq and mRNA-seq of activating transcription factor 4 (ATF4) and C/EBP homologous protein (CHOP), key transcription factors downstream of p-eIF2α, demonstrated that they interact to directly induce genes encoding protein synthesis and the unfolded protein response, but not apoptosis. Forced expression of ATF4 and CHOP increased protein synthesis and caused ATP depletion, oxidative stress and cell death. The increased protein synthesis and oxidative stress were necessary signals for cell death. We show that eIF2α-phosphorylation-attenuated protein synthesis, and not Atf4 mRNA translation, promotes cell survival. These results show that transcriptional induction through ATF4 and CHOP increases protein synthesis leading to oxidative stress and cell death. The findings suggest that limiting protein synthesis will be therapeutic for diseases caused by protein misfolding in the ER.
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            Distinct stages in stress granule assembly and disassembly

            Stress granules are non-membrane bound RNA-protein (RNP) assemblies that form when translation initiation is limited and contain a biphasic structure with stable core structures surrounded by a less concentrated shell. The order of assembly and disassembly of these two structures remains unknown. Time course analysis of granule assembly suggests that core formation is an early event in granule assembly. Stress granule disassembly is also a stepwise process with shell dissipation followed by core clearance. Perturbations that alter liquid-liquid phase separations (LLPS) driven by intrinsically disordered protein regions (IDR) of RNA binding proteins in vitro have the opposite effect on stress granule assembly in vivo. Taken together, these observations argue that stress granules assemble through a multistep process initiated by stable assembly of untranslated mRNPs into core structures, which could provide sufficient high local concentrations to allow for a localized LLPS driven by IDRs on RNA binding proteins. DOI: http://dx.doi.org/10.7554/eLife.18413.001
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              The eIF2α kinases: their structures and functions.

              Cell signaling in response to an array of diverse stress stimuli converges on the phosphorylation of the α-subunit of eukaryotic initiation factor 2 (eIF2). Phosphorylation of eIF2α on serine 51 results in a severe decline in de novo protein synthesis and is an important strategy in the cell's armory against stressful insults including viral infection, the accumulation of misfolded proteins, and starvation. The phosphorylation of eIF2α is carried out by a family of four kinases, PERK (PKR-like ER kinase), PKR (protein kinase double-stranded RNA-dependent), GCN2 (general control non-derepressible-2), and HRI (heme-regulated inhibitor). Each primarily responds to a distinct type of stress or stresses. Thus, while significant sequence similarity exists between the eIF2α kinases in their kinase domains, underlying their common role in phosphorylating eIF2α, additional unique features determine the regulation of these four proteins, that is, what signals activate them. This review will describe the structure of each eIF2α kinase and discuss how this is linked to their activation and function. In parallel to the general translational attenuation elicited by eIF2α kinase activation the translation of stress-induced mRNAs, most notably activating transcription factor 4 (ATF4) is enhanced and these set in motion cascades of gene expression constituting the integrated stress response (ISR), which seek to remediate stress and restore homeostasis. Depending on the cellular context and concurrent signaling pathways active, however, translational attenuation can also facilitate apoptosis. Accordingly, the role of the kinases in determining cell fate will also be discussed.
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                Author and article information

                Journal
                Anim Cells Syst (Seoul)
                Anim Cells Syst (Seoul)
                Animal Cells and Systems
                Taylor & Francis
                1976-8354
                2151-2485
                23 August 2023
                2023
                23 August 2023
                : 27
                : 1
                : 171-179
                Affiliations
                [a ]Department of Biochemistry, College of Natural Sciences, Chungnam National University , Daejeon, Republic of Korea
                [b ]Department of Predictive Toxicology, Korea Institute of Toxicology , Daejeon, Republic of Korea
                Author notes
                [CONTACT ] Kee K. Kim kimkk@ 123456cnu.ac.kr Department of Biochemistry, College of Natural Sciences, Chungnam National University , Daejeon 34134, Republic of Korea
                Eun-Mi Kim eunmi.kim@ 123456kitox.re.kr Department of Predictive Toxicology, Korea Institute of Toxicology , Daejeon 34114, Republic of Korea
                Author information
                https://orcid.org/0000-0002-1088-3383
                Article
                2250852
                10.1080/19768354.2023.2250852
                10448836
                37636324
                d24e80b0-dd6e-4475-8962-fee93cda5f2b
                © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://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.

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                Page count
                Figures: 4, Tables: 0, Equations: 1, References: 33, Pages: 9
                Categories
                Research Article
                Research Article

                chloromethylisothiazolinone,keratinocyte,protein kinase r-like endoplasmic reticulum kinase,endoplasmic reticulum-stress,stress granule

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