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The sarin-like organophosphorus agent bis(isopropyl methyl)phosphonate induces ER stress in human astrocytoma cells

Organophosphorus (OP) compounds such as sarin are toxic agents that irreversibly inhibit the enzyme acetylcholinesterase. A recent study showed that OP compounds also have multiple toxicity mechanisms, and another suggested that endoplasmic reticulum (ER) dysfunction contributes to OP toxicity. Howe...

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Published in:Journal of toxicological sciences 2016/10/01, Vol.41(5), pp.617-625
Main Authors: Arima, Yosuke, Shiraishi, Hiroaki, Saito, Atsushi, Yoshimoto, Kanji, Namera, Akira, Makita, Ryosuke, Murata, Kazuhiro, Imaizumi, Kazunori, Nagao, Masataka
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creator Arima, Yosuke
Shiraishi, Hiroaki
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Imaizumi, Kazunori
Nagao, Masataka
description Organophosphorus (OP) compounds such as sarin are toxic agents that irreversibly inhibit the enzyme acetylcholinesterase. A recent study showed that OP compounds also have multiple toxicity mechanisms, and another suggested that endoplasmic reticulum (ER) dysfunction contributes to OP toxicity. However, the signaling pathway and mechanisms involved are poorly understood. We examined whether the sarin-like OP agent bis(isopropyl methyl)phosphonate (BIMP), which exhibits toxicity similar to that of sarin, induced ER stress in human astrocytoma CCF-STTG1 cells. Our results demonstrate that BIMP exposure reduced cell viability. Moreover, it induced changes in mitochondrial membrane potential and increased cleavage of caspase 3. Treatment with BIMP increased the mRNA levels of the ER stress marker genes binding immunoglobulin protein (BiP) and the transcription factor C/EBP homologous protein (CHOP). Furthermore, BIMP increased the protein expressions and phosphorylation of BiP, CHOP, and protein kinase RNA-like ER kinase and the phosphorylation of eukaryotic translation initiation factor 2. Compared to BIMP treatment alone, pretreatment with the CHOP siRNA, siCHOP, decreased BIMP-dependent CHOP expression and improved CCF-STTG1 cell viability. Our findings suggest that BIMP induced mitochondrial dysfunction and apoptotic cell death event mediated by ER stress in CCF-STTG1 cells and that treatment targeted at managing ER stress has the potential to attenuate the toxicity of OP nerve agents.
doi_str_mv 10.2131/jts.41.617
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A recent study showed that OP compounds also have multiple toxicity mechanisms, and another suggested that endoplasmic reticulum (ER) dysfunction contributes to OP toxicity. However, the signaling pathway and mechanisms involved are poorly understood. We examined whether the sarin-like OP agent bis(isopropyl methyl)phosphonate (BIMP), which exhibits toxicity similar to that of sarin, induced ER stress in human astrocytoma CCF-STTG1 cells. Our results demonstrate that BIMP exposure reduced cell viability. Moreover, it induced changes in mitochondrial membrane potential and increased cleavage of caspase 3. Treatment with BIMP increased the mRNA levels of the ER stress marker genes binding immunoglobulin protein (BiP) and the transcription factor C/EBP homologous protein (CHOP). Furthermore, BIMP increased the protein expressions and phosphorylation of BiP, CHOP, and protein kinase RNA-like ER kinase and the phosphorylation of eukaryotic translation initiation factor 2. 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Compared to BIMP treatment alone, pretreatment with the CHOP siRNA, siCHOP, decreased BIMP-dependent CHOP expression and improved CCF-STTG1 cell viability. Our findings suggest that BIMP induced mitochondrial dysfunction and apoptotic cell death event mediated by ER stress in CCF-STTG1 cells and that treatment targeted at managing ER stress has the potential to attenuate the toxicity of OP nerve agents.</abstract><cop>Japan</cop><pub>The Japanese Society of Toxicology</pub><pmid>27665771</pmid><doi>10.2131/jts.41.617</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Acetylcholinesterase
Apoptosis
Astrocytes
Astrocytoma
Astrocytoma - genetics
Astrocytoma - metabolism
Astrocytoma - pathology
Bis(isopropyl methyl)phosphonate
Caspase
Caspase 3 - metabolism
Caspase-3
CCAAT/enhancer-binding protein
Cell death
Cell Line, Tumor
Cell Survival - drug effects
Cell viability
CHOP
Diphosphonates - toxicity
Dose-Response Relationship, Drug
eIF-2 Kinase - metabolism
Endoplasmic reticulum
Endoplasmic Reticulum Stress - drug effects
ER stress
Eukaryotic Initiation Factor-2 - metabolism
Gene Expression Regulation, Neoplastic
Heat-Shock Proteins - genetics
Heat-Shock Proteins - metabolism
Homology
Humans
Initiation factor eIF-2
Kinases
Membrane potential
Membrane Potential, Mitochondrial - drug effects
Mitochondria
Mitochondria - drug effects
Mitochondria - metabolism
Mitochondria - pathology
Nerve agents
Organophosphate Poisoning - etiology
Organophosphate Poisoning - metabolism
Organophosphate Poisoning - pathology
Organophosphates
Phosphonates
Phosphorylation
Pretreatment
Protein kinase
Proteins
RNA Interference
Sarin
Signal transduction
Signal Transduction - drug effects
siRNA
Stress
Time Factors
Toxicity
Transcription Factor CHOP - genetics
Transcription Factor CHOP - metabolism
Transfection
title The sarin-like organophosphorus agent bis(isopropyl methyl)phosphonate induces ER stress in human astrocytoma cells
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