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Peroxiredoxin 5 prevents diethylhexyl phthalate-induced neuronal cell death by inhibiting mitochondrial fission in mouse hippocampal HT-22 cells
•Diethylhexyl phthalate (DEHP) induces neurotoxicity through mitochondrial fission in HT-22 cells.•DEHP-induced oxidative stress triggers neuronal cell death via mitochondrial fission in HT-22 cells.•DEHP increases the expression levels of Peroxiredoxin 5 (Prx5).•Prx5 ameliorates DEHP-induced neurot...
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Published in: | Neurotoxicology (Park Forest South) 2019-09, Vol.74, p.242-251 |
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creator | Lee, Dong Gil Kim, Kyung-Min Lee, Hyun-Shik Bae, Yong Chul Huh, Jae-Won Lee, Sang-Rae Lee, Dong-Seok |
description | •Diethylhexyl phthalate (DEHP) induces neurotoxicity through mitochondrial fission in HT-22 cells.•DEHP-induced oxidative stress triggers neuronal cell death via mitochondrial fission in HT-22 cells.•DEHP increases the expression levels of Peroxiredoxin 5 (Prx5).•Prx5 ameliorates DEHP-induced neurotoxicity by inhibiting mitochondrial fission.
Diethylhexyl phthalate (DEHP) is used in many plastic products, such as perfumes, lunch boxes, bags, and building materials. As DEHP is not covalently bound to the plastic, humans can be easily exposed to it. DEHP induces neurobehavioral changes and neuronal cell death; however, the exact mechanism behind this is still unclear. We hypothesized that the neurotoxic mechanism is related to DEHP-induced oxidative stress leading to apoptosis through mitochondrial fission. We demonstrated that DEHP-induced oxidative stress triggers neuronal cell death via mitochondrial fission in mouse hippocampal HT-22 cells. Furthermore, we identified that peroxiredoxin 5 (Prx5), an antioxidant enzyme induced by DEHP, prevents DEHP-induced mitochondrial fission by inhibiting the production of reactive oxygen species. We conclude that Prx5 may be a promising therapeutic target for mitigating DEHP-induced neuronal cell death. |
doi_str_mv | 10.1016/j.neuro.2019.08.003 |
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Diethylhexyl phthalate (DEHP) is used in many plastic products, such as perfumes, lunch boxes, bags, and building materials. As DEHP is not covalently bound to the plastic, humans can be easily exposed to it. DEHP induces neurobehavioral changes and neuronal cell death; however, the exact mechanism behind this is still unclear. We hypothesized that the neurotoxic mechanism is related to DEHP-induced oxidative stress leading to apoptosis through mitochondrial fission. We demonstrated that DEHP-induced oxidative stress triggers neuronal cell death via mitochondrial fission in mouse hippocampal HT-22 cells. Furthermore, we identified that peroxiredoxin 5 (Prx5), an antioxidant enzyme induced by DEHP, prevents DEHP-induced mitochondrial fission by inhibiting the production of reactive oxygen species. We conclude that Prx5 may be a promising therapeutic target for mitigating DEHP-induced neuronal cell death.</description><identifier>ISSN: 0161-813X</identifier><identifier>EISSN: 1872-9711</identifier><identifier>DOI: 10.1016/j.neuro.2019.08.003</identifier><identifier>PMID: 31408635</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Antioxidants ; Apoptosis ; Apoptosis - genetics ; Building materials ; Cell death ; Cell Death - genetics ; Cell Line ; Construction materials ; Diethylhexyl phthalate ; Diethylhexyl Phthalate - toxicity ; Dioctyl phthalate ; Fission ; Gene Knockdown Techniques ; Hippocampus ; Hippocampus - drug effects ; Hippocampus - metabolism ; Hippocampus - pathology ; Mice ; Mitochondria ; Mitochondria - genetics ; Mitochondria - ultrastructure ; Mitochondrial dynamics ; Mortality ; Neurons - drug effects ; Neurons - pathology ; Neurotoxicity ; Oxidation ; Oxidative stress ; Oxidative Stress - drug effects ; Perfumes ; Peroxiredoxin ; Peroxiredoxin 5 ; Peroxiredoxins - genetics ; Peroxiredoxins - pharmacology ; Phthalates ; Reactive Oxygen Species ; Therapeutic applications</subject><ispartof>Neurotoxicology (Park Forest South), 2019-09, Vol.74, p.242-251</ispartof><rights>2019 Elsevier B.V.</rights><rights>Copyright © 2019 Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier BV Sep 2019</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c387t-1615e6cbbe6b410e124179f470c5d46b2850ac90b9e42598f64954032b63e0293</citedby><cites>FETCH-LOGICAL-c387t-1615e6cbbe6b410e124179f470c5d46b2850ac90b9e42598f64954032b63e0293</cites><orcidid>0000-0002-7106-1615</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31408635$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lee, Dong Gil</creatorcontrib><creatorcontrib>Kim, Kyung-Min</creatorcontrib><creatorcontrib>Lee, Hyun-Shik</creatorcontrib><creatorcontrib>Bae, Yong Chul</creatorcontrib><creatorcontrib>Huh, Jae-Won</creatorcontrib><creatorcontrib>Lee, Sang-Rae</creatorcontrib><creatorcontrib>Lee, Dong-Seok</creatorcontrib><title>Peroxiredoxin 5 prevents diethylhexyl phthalate-induced neuronal cell death by inhibiting mitochondrial fission in mouse hippocampal HT-22 cells</title><title>Neurotoxicology (Park Forest South)</title><addtitle>Neurotoxicology</addtitle><description>•Diethylhexyl phthalate (DEHP) induces neurotoxicity through mitochondrial fission in HT-22 cells.•DEHP-induced oxidative stress triggers neuronal cell death via mitochondrial fission in HT-22 cells.•DEHP increases the expression levels of Peroxiredoxin 5 (Prx5).•Prx5 ameliorates DEHP-induced neurotoxicity by inhibiting mitochondrial fission.
Diethylhexyl phthalate (DEHP) is used in many plastic products, such as perfumes, lunch boxes, bags, and building materials. As DEHP is not covalently bound to the plastic, humans can be easily exposed to it. DEHP induces neurobehavioral changes and neuronal cell death; however, the exact mechanism behind this is still unclear. We hypothesized that the neurotoxic mechanism is related to DEHP-induced oxidative stress leading to apoptosis through mitochondrial fission. We demonstrated that DEHP-induced oxidative stress triggers neuronal cell death via mitochondrial fission in mouse hippocampal HT-22 cells. Furthermore, we identified that peroxiredoxin 5 (Prx5), an antioxidant enzyme induced by DEHP, prevents DEHP-induced mitochondrial fission by inhibiting the production of reactive oxygen species. We conclude that Prx5 may be a promising therapeutic target for mitigating DEHP-induced neuronal cell death.</description><subject>Animals</subject><subject>Antioxidants</subject><subject>Apoptosis</subject><subject>Apoptosis - genetics</subject><subject>Building materials</subject><subject>Cell death</subject><subject>Cell Death - genetics</subject><subject>Cell Line</subject><subject>Construction materials</subject><subject>Diethylhexyl phthalate</subject><subject>Diethylhexyl Phthalate - toxicity</subject><subject>Dioctyl phthalate</subject><subject>Fission</subject><subject>Gene Knockdown Techniques</subject><subject>Hippocampus</subject><subject>Hippocampus - drug effects</subject><subject>Hippocampus - metabolism</subject><subject>Hippocampus - pathology</subject><subject>Mice</subject><subject>Mitochondria</subject><subject>Mitochondria - genetics</subject><subject>Mitochondria - ultrastructure</subject><subject>Mitochondrial dynamics</subject><subject>Mortality</subject><subject>Neurons - drug effects</subject><subject>Neurons - pathology</subject><subject>Neurotoxicity</subject><subject>Oxidation</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - drug effects</subject><subject>Perfumes</subject><subject>Peroxiredoxin</subject><subject>Peroxiredoxin 5</subject><subject>Peroxiredoxins - genetics</subject><subject>Peroxiredoxins - pharmacology</subject><subject>Phthalates</subject><subject>Reactive Oxygen Species</subject><subject>Therapeutic applications</subject><issn>0161-813X</issn><issn>1872-9711</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kU1v1DAQhi1ERbcLvwAJWeLCJen4I18HDqgCilQJDkXiZiXOhHiV2MF2qu6_6E_Gu9ty4NCL5-Bn3pl5X0LeMsgZsPJyl1tcvcs5sCaHOgcQL8iG1RXPmoqxl2STKJbVTPw6Jxch7ABYUZXNK3IumIS6FMWGPPxA7-6Nxz69lhZ08XiHNgbaG4zjfhrxfj_RZYxjO7URM2P7VWNPj7NtO1GN00R7bONIuz01djSdicb-prOJTo_O9t4kbDAhGGcTQGe3BqSjWRan23lJn9e3GedHpfCanA3tFPDNY92Sn18-315dZzffv367-nSTaVFXMUuXFVjqrsOykwyQccmqZpAV6KKXZcfrAlrdQNeg5EVTD6VsCgmCd6VA4I3Ykg8n3cW7PyuGqGYTDhu0FtN-ivNKcJBlcnVL3v-H7tzq0-2JEsl8JkDKRIkTpb0LweOgFm_m1u8VA3UITO3U0TR1CExBrZJ06nr3qL12M_b_ep4SSsDHE4DJjDuDXgVt0KYIUmg6qt6ZZwf8BV-4qVE</recordid><startdate>201909</startdate><enddate>201909</enddate><creator>Lee, Dong Gil</creator><creator>Kim, Kyung-Min</creator><creator>Lee, Hyun-Shik</creator><creator>Bae, Yong Chul</creator><creator>Huh, Jae-Won</creator><creator>Lee, Sang-Rae</creator><creator>Lee, Dong-Seok</creator><general>Elsevier B.V</general><general>Elsevier BV</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>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-7106-1615</orcidid></search><sort><creationdate>201909</creationdate><title>Peroxiredoxin 5 prevents diethylhexyl phthalate-induced neuronal cell death by inhibiting mitochondrial fission in mouse hippocampal HT-22 cells</title><author>Lee, Dong Gil ; Kim, Kyung-Min ; Lee, Hyun-Shik ; Bae, Yong Chul ; Huh, Jae-Won ; Lee, Sang-Rae ; Lee, Dong-Seok</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c387t-1615e6cbbe6b410e124179f470c5d46b2850ac90b9e42598f64954032b63e0293</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Animals</topic><topic>Antioxidants</topic><topic>Apoptosis</topic><topic>Apoptosis - genetics</topic><topic>Building materials</topic><topic>Cell death</topic><topic>Cell Death - genetics</topic><topic>Cell Line</topic><topic>Construction materials</topic><topic>Diethylhexyl phthalate</topic><topic>Diethylhexyl Phthalate - toxicity</topic><topic>Dioctyl phthalate</topic><topic>Fission</topic><topic>Gene Knockdown Techniques</topic><topic>Hippocampus</topic><topic>Hippocampus - drug effects</topic><topic>Hippocampus - metabolism</topic><topic>Hippocampus - pathology</topic><topic>Mice</topic><topic>Mitochondria</topic><topic>Mitochondria - genetics</topic><topic>Mitochondria - ultrastructure</topic><topic>Mitochondrial dynamics</topic><topic>Mortality</topic><topic>Neurons - drug effects</topic><topic>Neurons - pathology</topic><topic>Neurotoxicity</topic><topic>Oxidation</topic><topic>Oxidative stress</topic><topic>Oxidative Stress - drug effects</topic><topic>Perfumes</topic><topic>Peroxiredoxin</topic><topic>Peroxiredoxin 5</topic><topic>Peroxiredoxins - genetics</topic><topic>Peroxiredoxins - pharmacology</topic><topic>Phthalates</topic><topic>Reactive Oxygen Species</topic><topic>Therapeutic applications</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lee, Dong Gil</creatorcontrib><creatorcontrib>Kim, Kyung-Min</creatorcontrib><creatorcontrib>Lee, Hyun-Shik</creatorcontrib><creatorcontrib>Bae, Yong Chul</creatorcontrib><creatorcontrib>Huh, Jae-Won</creatorcontrib><creatorcontrib>Lee, Sang-Rae</creatorcontrib><creatorcontrib>Lee, Dong-Seok</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>MEDLINE - Academic</collection><jtitle>Neurotoxicology (Park Forest South)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lee, Dong Gil</au><au>Kim, Kyung-Min</au><au>Lee, Hyun-Shik</au><au>Bae, Yong Chul</au><au>Huh, Jae-Won</au><au>Lee, Sang-Rae</au><au>Lee, Dong-Seok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Peroxiredoxin 5 prevents diethylhexyl phthalate-induced neuronal cell death by inhibiting mitochondrial fission in mouse hippocampal HT-22 cells</atitle><jtitle>Neurotoxicology (Park Forest South)</jtitle><addtitle>Neurotoxicology</addtitle><date>2019-09</date><risdate>2019</risdate><volume>74</volume><spage>242</spage><epage>251</epage><pages>242-251</pages><issn>0161-813X</issn><eissn>1872-9711</eissn><abstract>•Diethylhexyl phthalate (DEHP) induces neurotoxicity through mitochondrial fission in HT-22 cells.•DEHP-induced oxidative stress triggers neuronal cell death via mitochondrial fission in HT-22 cells.•DEHP increases the expression levels of Peroxiredoxin 5 (Prx5).•Prx5 ameliorates DEHP-induced neurotoxicity by inhibiting mitochondrial fission.
Diethylhexyl phthalate (DEHP) is used in many plastic products, such as perfumes, lunch boxes, bags, and building materials. As DEHP is not covalently bound to the plastic, humans can be easily exposed to it. DEHP induces neurobehavioral changes and neuronal cell death; however, the exact mechanism behind this is still unclear. We hypothesized that the neurotoxic mechanism is related to DEHP-induced oxidative stress leading to apoptosis through mitochondrial fission. We demonstrated that DEHP-induced oxidative stress triggers neuronal cell death via mitochondrial fission in mouse hippocampal HT-22 cells. Furthermore, we identified that peroxiredoxin 5 (Prx5), an antioxidant enzyme induced by DEHP, prevents DEHP-induced mitochondrial fission by inhibiting the production of reactive oxygen species. We conclude that Prx5 may be a promising therapeutic target for mitigating DEHP-induced neuronal cell death.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>31408635</pmid><doi>10.1016/j.neuro.2019.08.003</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-7106-1615</orcidid></addata></record> |
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subjects | Animals Antioxidants Apoptosis Apoptosis - genetics Building materials Cell death Cell Death - genetics Cell Line Construction materials Diethylhexyl phthalate Diethylhexyl Phthalate - toxicity Dioctyl phthalate Fission Gene Knockdown Techniques Hippocampus Hippocampus - drug effects Hippocampus - metabolism Hippocampus - pathology Mice Mitochondria Mitochondria - genetics Mitochondria - ultrastructure Mitochondrial dynamics Mortality Neurons - drug effects Neurons - pathology Neurotoxicity Oxidation Oxidative stress Oxidative Stress - drug effects Perfumes Peroxiredoxin Peroxiredoxin 5 Peroxiredoxins - genetics Peroxiredoxins - pharmacology Phthalates Reactive Oxygen Species Therapeutic applications |
title | Peroxiredoxin 5 prevents diethylhexyl phthalate-induced neuronal cell death by inhibiting mitochondrial fission in mouse hippocampal HT-22 cells |
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