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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 |
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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. 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.</description><identifier>ISSN: 0388-1350</identifier><identifier>EISSN: 1880-3989</identifier><identifier>DOI: 10.2131/jts.41.617</identifier><identifier>PMID: 27665771</identifier><language>eng</language><publisher>Japan: The Japanese Society of Toxicology</publisher><subject>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</subject><ispartof>The Journal of Toxicological Sciences, 2016/10/01, Vol.41(5), pp.617-625</ispartof><rights>2016 The Japanese Society of Toxicology</rights><rights>Copyright Japan Science and Technology Agency Oct 2016</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c623t-7158e993be49504b80e36da5e98cb08af419d3ec23cdfa488b4b0d3a2af9f39c3</citedby><cites>FETCH-LOGICAL-c623t-7158e993be49504b80e36da5e98cb08af419d3ec23cdfa488b4b0d3a2af9f39c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,4010,27902,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27665771$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Arima, Yosuke</creatorcontrib><creatorcontrib>Shiraishi, Hiroaki</creatorcontrib><creatorcontrib>Saito, Atsushi</creatorcontrib><creatorcontrib>Yoshimoto, Kanji</creatorcontrib><creatorcontrib>Namera, Akira</creatorcontrib><creatorcontrib>Makita, Ryosuke</creatorcontrib><creatorcontrib>Murata, Kazuhiro</creatorcontrib><creatorcontrib>Imaizumi, Kazunori</creatorcontrib><creatorcontrib>Nagao, Masataka</creatorcontrib><title>The sarin-like organophosphorus agent bis(isopropyl methyl)phosphonate induces ER stress in human astrocytoma cells</title><title>Journal of toxicological sciences</title><addtitle>J Toxicol Sci</addtitle><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.</description><subject>Acetylcholinesterase</subject><subject>Apoptosis</subject><subject>Astrocytes</subject><subject>Astrocytoma</subject><subject>Astrocytoma - genetics</subject><subject>Astrocytoma - metabolism</subject><subject>Astrocytoma - pathology</subject><subject>Bis(isopropyl methyl)phosphonate</subject><subject>Caspase</subject><subject>Caspase 3 - metabolism</subject><subject>Caspase-3</subject><subject>CCAAT/enhancer-binding protein</subject><subject>Cell death</subject><subject>Cell Line, Tumor</subject><subject>Cell Survival - drug effects</subject><subject>Cell viability</subject><subject>CHOP</subject><subject>Diphosphonates - toxicity</subject><subject>Dose-Response Relationship, Drug</subject><subject>eIF-2 Kinase - metabolism</subject><subject>Endoplasmic reticulum</subject><subject>Endoplasmic Reticulum Stress - drug effects</subject><subject>ER stress</subject><subject>Eukaryotic Initiation Factor-2 - metabolism</subject><subject>Gene Expression Regulation, Neoplastic</subject><subject>Heat-Shock Proteins - genetics</subject><subject>Heat-Shock Proteins - metabolism</subject><subject>Homology</subject><subject>Humans</subject><subject>Initiation factor eIF-2</subject><subject>Kinases</subject><subject>Membrane potential</subject><subject>Membrane Potential, Mitochondrial - drug effects</subject><subject>Mitochondria</subject><subject>Mitochondria - drug effects</subject><subject>Mitochondria - metabolism</subject><subject>Mitochondria - pathology</subject><subject>Nerve agents</subject><subject>Organophosphate Poisoning - etiology</subject><subject>Organophosphate Poisoning - metabolism</subject><subject>Organophosphate Poisoning - pathology</subject><subject>Organophosphates</subject><subject>Phosphonates</subject><subject>Phosphorylation</subject><subject>Pretreatment</subject><subject>Protein kinase</subject><subject>Proteins</subject><subject>RNA Interference</subject><subject>Sarin</subject><subject>Signal transduction</subject><subject>Signal Transduction - drug effects</subject><subject>siRNA</subject><subject>Stress</subject><subject>Time Factors</subject><subject>Toxicity</subject><subject>Transcription Factor CHOP - genetics</subject><subject>Transcription Factor CHOP - metabolism</subject><subject>Transfection</subject><issn>0388-1350</issn><issn>1880-3989</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNpdkU9r3DAUxEVpaTZpL_0ARdBLWvBWfyxbOvRQQtIWAoWSnoUsP8fe2tJWTz7st6_CbvbQw-PB8GMYZgh5x9lWcMk_7zJua75tePuCbLjWrJJGm5dkw6TWFZeKXZBLxB1jomWqfk0uRNs0qm35huDDCBRdmkI1T3-AxvToQtyPEculFal7hJBpN-H1hHGf4v4w0wXyeJg_nqjgMtAp9KsHpLe_KOYEiEWh47q4QF0Roj_kuDjqYZ7xDXk1uBnh7elfkd93tw8336v7n99-3Hy9r3wjZK5arjQYIzuojWJ1pxnIpncKjPYd026ouekleCF9P7ha667uWC-dcIMZpPHyilwffUvsvytgtsuETwlcgLii5VpIw7RhrKAf_kN3cU2hpLNCSNUoxaUu1Kcj5VNETDDYfZoWlw6WM_s0hS1T2JrbMkWB358s126B_ow-d1-AL0dgh7m0fAZcypOf4dlLnQzPuh9dshDkP5DVnTk</recordid><startdate>2016</startdate><enddate>2016</enddate><creator>Arima, Yosuke</creator><creator>Shiraishi, Hiroaki</creator><creator>Saito, Atsushi</creator><creator>Yoshimoto, Kanji</creator><creator>Namera, Akira</creator><creator>Makita, Ryosuke</creator><creator>Murata, Kazuhiro</creator><creator>Imaizumi, Kazunori</creator><creator>Nagao, Masataka</creator><general>The Japanese Society of Toxicology</general><general>Japan Science and Technology Agency</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7U7</scope><scope>C1K</scope><scope>SOI</scope><scope>7X8</scope></search><sort><creationdate>2016</creationdate><title>The sarin-like organophosphorus agent bis(isopropyl methyl)phosphonate induces ER stress in human astrocytoma cells</title><author>Arima, Yosuke ; Shiraishi, Hiroaki ; Saito, Atsushi ; Yoshimoto, Kanji ; Namera, Akira ; Makita, Ryosuke ; Murata, Kazuhiro ; Imaizumi, Kazunori ; Nagao, Masataka</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c623t-7158e993be49504b80e36da5e98cb08af419d3ec23cdfa488b4b0d3a2af9f39c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Acetylcholinesterase</topic><topic>Apoptosis</topic><topic>Astrocytes</topic><topic>Astrocytoma</topic><topic>Astrocytoma - genetics</topic><topic>Astrocytoma - metabolism</topic><topic>Astrocytoma - pathology</topic><topic>Bis(isopropyl methyl)phosphonate</topic><topic>Caspase</topic><topic>Caspase 3 - metabolism</topic><topic>Caspase-3</topic><topic>CCAAT/enhancer-binding protein</topic><topic>Cell death</topic><topic>Cell Line, Tumor</topic><topic>Cell Survival - drug effects</topic><topic>Cell viability</topic><topic>CHOP</topic><topic>Diphosphonates - toxicity</topic><topic>Dose-Response Relationship, Drug</topic><topic>eIF-2 Kinase - metabolism</topic><topic>Endoplasmic reticulum</topic><topic>Endoplasmic Reticulum Stress - drug effects</topic><topic>ER stress</topic><topic>Eukaryotic Initiation Factor-2 - metabolism</topic><topic>Gene Expression Regulation, Neoplastic</topic><topic>Heat-Shock Proteins - genetics</topic><topic>Heat-Shock Proteins - metabolism</topic><topic>Homology</topic><topic>Humans</topic><topic>Initiation factor eIF-2</topic><topic>Kinases</topic><topic>Membrane potential</topic><topic>Membrane Potential, Mitochondrial - drug effects</topic><topic>Mitochondria</topic><topic>Mitochondria - drug effects</topic><topic>Mitochondria - metabolism</topic><topic>Mitochondria - pathology</topic><topic>Nerve agents</topic><topic>Organophosphate Poisoning - etiology</topic><topic>Organophosphate Poisoning - metabolism</topic><topic>Organophosphate Poisoning - pathology</topic><topic>Organophosphates</topic><topic>Phosphonates</topic><topic>Phosphorylation</topic><topic>Pretreatment</topic><topic>Protein kinase</topic><topic>Proteins</topic><topic>RNA Interference</topic><topic>Sarin</topic><topic>Signal transduction</topic><topic>Signal Transduction - drug effects</topic><topic>siRNA</topic><topic>Stress</topic><topic>Time Factors</topic><topic>Toxicity</topic><topic>Transcription Factor CHOP - genetics</topic><topic>Transcription Factor CHOP - metabolism</topic><topic>Transfection</topic><toplevel>online_resources</toplevel><creatorcontrib>Arima, Yosuke</creatorcontrib><creatorcontrib>Shiraishi, Hiroaki</creatorcontrib><creatorcontrib>Saito, Atsushi</creatorcontrib><creatorcontrib>Yoshimoto, Kanji</creatorcontrib><creatorcontrib>Namera, Akira</creatorcontrib><creatorcontrib>Makita, Ryosuke</creatorcontrib><creatorcontrib>Murata, Kazuhiro</creatorcontrib><creatorcontrib>Imaizumi, Kazunori</creatorcontrib><creatorcontrib>Nagao, Masataka</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Environment Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of toxicological sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Arima, Yosuke</au><au>Shiraishi, Hiroaki</au><au>Saito, Atsushi</au><au>Yoshimoto, Kanji</au><au>Namera, Akira</au><au>Makita, Ryosuke</au><au>Murata, Kazuhiro</au><au>Imaizumi, Kazunori</au><au>Nagao, Masataka</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The sarin-like organophosphorus agent bis(isopropyl methyl)phosphonate induces ER stress in human astrocytoma cells</atitle><jtitle>Journal of toxicological sciences</jtitle><addtitle>J Toxicol Sci</addtitle><date>2016</date><risdate>2016</risdate><volume>41</volume><issue>5</issue><spage>617</spage><epage>625</epage><pages>617-625</pages><issn>0388-1350</issn><eissn>1880-3989</eissn><abstract>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.</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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