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2-IPMA Ameliorates PM2.5-Induced Inflammation by Promoting Primary Ciliogenesis in RPE Cells
Primary cilia mediate the interactions between cells and external stresses. Thus, dysregulation of primary cilia is implicated in various ciliopathies, e.g., degeneration of the retina caused by dysregulation of the photoreceptor primary cilium. Particulate matter (PM) can cause epithelium injury an...
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Published in: | Molecules (Basel, Switzerland) Switzerland), 2021-09, Vol.26 (17), p.5409 |
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creator | Choi, Ji Yeon Bae, Ji-Eun Kim, Joon Bum Jo, Doo Sin Park, Na Yeon Kim, Yong Hwan Lee, Ha Jung Kim, Seong Hyun Kim, So Hyun Jeon, Hong Bae Choi, Hyungjung Ryu, Hong-Yeoul Ryoo, Zae Young Lee, Hyun-Shik Cho, Dong-Hyung |
description | Primary cilia mediate the interactions between cells and external stresses. Thus, dysregulation of primary cilia is implicated in various ciliopathies, e.g., degeneration of the retina caused by dysregulation of the photoreceptor primary cilium. Particulate matter (PM) can cause epithelium injury and endothelial dysfunction by increasing oxidative stress and inflammatory responses. Previously, we showed that PM disrupts the formation of primary cilia in retinal pigment epithelium (RPE) cells. In the present study, we identified 2-isopropylmalic acid (2-IPMA) as a novel inducer of primary ciliogenesis from a metabolite library screening. Both ciliated cells and primary cilium length were increased in 2-IPMA-treated RPE cells. Notably, 2-IPMA strongly promoted primary ciliogenesis and restored PM2.5-induced dysgenesis of primary cilia in RPE cells. Both excessive reactive oxygen species (ROS) generation and activation of a stress kinase, JNK, by PM2.5 were reduced by 2-IPMA. Moreover, 2-IPMA inhibited proinflammatory cytokine production, i.e., IL-6 and TNF-α, induced by PM2.5 in RPE cells. Taken together, our data suggest that 2-IPMA ameliorates PM2.5-induced inflammation by promoting primary ciliogenesis in RPE cells. |
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Thus, dysregulation of primary cilia is implicated in various ciliopathies, e.g., degeneration of the retina caused by dysregulation of the photoreceptor primary cilium. Particulate matter (PM) can cause epithelium injury and endothelial dysfunction by increasing oxidative stress and inflammatory responses. Previously, we showed that PM disrupts the formation of primary cilia in retinal pigment epithelium (RPE) cells. In the present study, we identified 2-isopropylmalic acid (2-IPMA) as a novel inducer of primary ciliogenesis from a metabolite library screening. Both ciliated cells and primary cilium length were increased in 2-IPMA-treated RPE cells. Notably, 2-IPMA strongly promoted primary ciliogenesis and restored PM2.5-induced dysgenesis of primary cilia in RPE cells. Both excessive reactive oxygen species (ROS) generation and activation of a stress kinase, JNK, by PM2.5 were reduced by 2-IPMA. Moreover, 2-IPMA inhibited proinflammatory cytokine production, i.e., IL-6 and TNF-α, induced by PM2.5 in RPE cells. Taken together, our data suggest that 2-IPMA ameliorates PM2.5-induced inflammation by promoting primary ciliogenesis in RPE cells.</description><identifier>ISSN: 1420-3049</identifier><identifier>EISSN: 1420-3049</identifier><identifier>DOI: 10.3390/molecules26175409</identifier><identifier>PMID: 34500843</identifier><language>eng</language><publisher>Basel: MDPI AG</publisher><subject>2-IPMA ; Air pollution ; Antibodies ; Apoptosis ; Cell culture ; Cell cycle ; Cilia ; Degeneration ; Epithelium ; Feces ; Gene expression ; Inflammation ; Interleukin 6 ; Libraries ; Metabolites ; Oxidative stress ; Particulate emissions ; Particulate matter ; particulate matter (PM2.5) ; primary cilia ; Proteins ; Reactive oxygen species ; Reagents ; Retina ; Retinal pigment epithelium ; RPE cells ; Signal transduction ; Software ; Stress measurement ; Tumor necrosis factor-α</subject><ispartof>Molecules (Basel, Switzerland), 2021-09, Vol.26 (17), p.5409</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c470t-d282520652d8c517919f05b3bbec21e006441113b54484d48a5d7b2a1ae5eaf83</citedby><cites>FETCH-LOGICAL-c470t-d282520652d8c517919f05b3bbec21e006441113b54484d48a5d7b2a1ae5eaf83</cites><orcidid>0000-0001-9319-5270 ; 0000-0002-3837-9867</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2571438385/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2571438385?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids></links><search><creatorcontrib>Choi, Ji Yeon</creatorcontrib><creatorcontrib>Bae, Ji-Eun</creatorcontrib><creatorcontrib>Kim, Joon Bum</creatorcontrib><creatorcontrib>Jo, Doo Sin</creatorcontrib><creatorcontrib>Park, Na Yeon</creatorcontrib><creatorcontrib>Kim, Yong Hwan</creatorcontrib><creatorcontrib>Lee, Ha Jung</creatorcontrib><creatorcontrib>Kim, Seong Hyun</creatorcontrib><creatorcontrib>Kim, So Hyun</creatorcontrib><creatorcontrib>Jeon, Hong Bae</creatorcontrib><creatorcontrib>Choi, Hyungjung</creatorcontrib><creatorcontrib>Ryu, Hong-Yeoul</creatorcontrib><creatorcontrib>Ryoo, Zae Young</creatorcontrib><creatorcontrib>Lee, Hyun-Shik</creatorcontrib><creatorcontrib>Cho, Dong-Hyung</creatorcontrib><title>2-IPMA Ameliorates PM2.5-Induced Inflammation by Promoting Primary Ciliogenesis in RPE Cells</title><title>Molecules (Basel, Switzerland)</title><description>Primary cilia mediate the interactions between cells and external stresses. Thus, dysregulation of primary cilia is implicated in various ciliopathies, e.g., degeneration of the retina caused by dysregulation of the photoreceptor primary cilium. Particulate matter (PM) can cause epithelium injury and endothelial dysfunction by increasing oxidative stress and inflammatory responses. Previously, we showed that PM disrupts the formation of primary cilia in retinal pigment epithelium (RPE) cells. In the present study, we identified 2-isopropylmalic acid (2-IPMA) as a novel inducer of primary ciliogenesis from a metabolite library screening. Both ciliated cells and primary cilium length were increased in 2-IPMA-treated RPE cells. Notably, 2-IPMA strongly promoted primary ciliogenesis and restored PM2.5-induced dysgenesis of primary cilia in RPE cells. Both excessive reactive oxygen species (ROS) generation and activation of a stress kinase, JNK, by PM2.5 were reduced by 2-IPMA. Moreover, 2-IPMA inhibited proinflammatory cytokine production, i.e., IL-6 and TNF-α, induced by PM2.5 in RPE cells. Taken together, our data suggest that 2-IPMA ameliorates PM2.5-induced inflammation by promoting primary ciliogenesis in RPE cells.</description><subject>2-IPMA</subject><subject>Air pollution</subject><subject>Antibodies</subject><subject>Apoptosis</subject><subject>Cell culture</subject><subject>Cell cycle</subject><subject>Cilia</subject><subject>Degeneration</subject><subject>Epithelium</subject><subject>Feces</subject><subject>Gene expression</subject><subject>Inflammation</subject><subject>Interleukin 6</subject><subject>Libraries</subject><subject>Metabolites</subject><subject>Oxidative stress</subject><subject>Particulate emissions</subject><subject>Particulate matter</subject><subject>particulate matter (PM2.5)</subject><subject>primary cilia</subject><subject>Proteins</subject><subject>Reactive oxygen species</subject><subject>Reagents</subject><subject>Retina</subject><subject>Retinal pigment epithelium</subject><subject>RPE cells</subject><subject>Signal transduction</subject><subject>Software</subject><subject>Stress measurement</subject><subject>Tumor necrosis factor-α</subject><issn>1420-3049</issn><issn>1420-3049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNplkltrFEEQhRtRzMX8AN8afPFlYl93ul-EZYnJQIKL6Fug6UvN2stMd-yeEfLvM8kGMfpURdWpj8OhEHpPyTnnmnwa8wB-HqCyFW2lIPoVOqaCkYYToV__1R-hk1r3hDAqqHyLjriQhCjBj9Eta7rtzRqvRxhiLnaCirc37Fw2XQqzh4C71A92HO0Uc8LuHm9LHvMU027p4mjLPd7E5XQHCWqsOCb8bXuBNzAM9R1609uhwtlzPUU_vlx831w1118vu836uvGiJVMTmGKSkZVkQXlJW011T6TjzoFnFAhZCUEp5U4KoUQQysrQOmapBQm2V_wUdQduyHZv7g62TLbRPA1y2RlbpugHMByYFtLa1gkiWqmdhqCEA62to7xvF9bnA-tudiMED2kqdngBfblJ8afZ5d9miZNrJhfAx2dAyb9mqJMZY_VLHDZBnqthsqWaMan4Iv3wj3Sf55KWqJ5UgiuuHoH0oPIl11qg_2OGEvP4B-a_P-AP7PKk5Q</recordid><startdate>20210906</startdate><enddate>20210906</enddate><creator>Choi, Ji Yeon</creator><creator>Bae, Ji-Eun</creator><creator>Kim, Joon Bum</creator><creator>Jo, Doo Sin</creator><creator>Park, Na Yeon</creator><creator>Kim, Yong Hwan</creator><creator>Lee, Ha Jung</creator><creator>Kim, Seong Hyun</creator><creator>Kim, So Hyun</creator><creator>Jeon, Hong Bae</creator><creator>Choi, Hyungjung</creator><creator>Ryu, Hong-Yeoul</creator><creator>Ryoo, Zae Young</creator><creator>Lee, Hyun-Shik</creator><creator>Cho, Dong-Hyung</creator><general>MDPI AG</general><general>MDPI</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-9319-5270</orcidid><orcidid>https://orcid.org/0000-0002-3837-9867</orcidid></search><sort><creationdate>20210906</creationdate><title>2-IPMA Ameliorates PM2.5-Induced Inflammation by Promoting Primary Ciliogenesis in RPE Cells</title><author>Choi, Ji Yeon ; Bae, Ji-Eun ; Kim, Joon Bum ; Jo, Doo Sin ; Park, Na Yeon ; Kim, Yong Hwan ; Lee, Ha Jung ; Kim, Seong Hyun ; Kim, So Hyun ; Jeon, Hong Bae ; Choi, Hyungjung ; Ryu, Hong-Yeoul ; Ryoo, Zae Young ; Lee, Hyun-Shik ; Cho, Dong-Hyung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c470t-d282520652d8c517919f05b3bbec21e006441113b54484d48a5d7b2a1ae5eaf83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>2-IPMA</topic><topic>Air pollution</topic><topic>Antibodies</topic><topic>Apoptosis</topic><topic>Cell culture</topic><topic>Cell cycle</topic><topic>Cilia</topic><topic>Degeneration</topic><topic>Epithelium</topic><topic>Feces</topic><topic>Gene expression</topic><topic>Inflammation</topic><topic>Interleukin 6</topic><topic>Libraries</topic><topic>Metabolites</topic><topic>Oxidative stress</topic><topic>Particulate emissions</topic><topic>Particulate matter</topic><topic>particulate matter (PM2.5)</topic><topic>primary cilia</topic><topic>Proteins</topic><topic>Reactive oxygen species</topic><topic>Reagents</topic><topic>Retina</topic><topic>Retinal pigment epithelium</topic><topic>RPE cells</topic><topic>Signal transduction</topic><topic>Software</topic><topic>Stress measurement</topic><topic>Tumor necrosis factor-α</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Choi, Ji Yeon</creatorcontrib><creatorcontrib>Bae, Ji-Eun</creatorcontrib><creatorcontrib>Kim, Joon Bum</creatorcontrib><creatorcontrib>Jo, Doo Sin</creatorcontrib><creatorcontrib>Park, Na Yeon</creatorcontrib><creatorcontrib>Kim, Yong Hwan</creatorcontrib><creatorcontrib>Lee, Ha Jung</creatorcontrib><creatorcontrib>Kim, Seong Hyun</creatorcontrib><creatorcontrib>Kim, So Hyun</creatorcontrib><creatorcontrib>Jeon, Hong Bae</creatorcontrib><creatorcontrib>Choi, Hyungjung</creatorcontrib><creatorcontrib>Ryu, Hong-Yeoul</creatorcontrib><creatorcontrib>Ryoo, Zae Young</creatorcontrib><creatorcontrib>Lee, Hyun-Shik</creatorcontrib><creatorcontrib>Cho, Dong-Hyung</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Molecules (Basel, Switzerland)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Choi, Ji Yeon</au><au>Bae, Ji-Eun</au><au>Kim, Joon Bum</au><au>Jo, Doo Sin</au><au>Park, Na Yeon</au><au>Kim, Yong Hwan</au><au>Lee, Ha Jung</au><au>Kim, Seong Hyun</au><au>Kim, So Hyun</au><au>Jeon, Hong Bae</au><au>Choi, Hyungjung</au><au>Ryu, Hong-Yeoul</au><au>Ryoo, Zae Young</au><au>Lee, Hyun-Shik</au><au>Cho, Dong-Hyung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>2-IPMA Ameliorates PM2.5-Induced Inflammation by Promoting Primary Ciliogenesis in RPE Cells</atitle><jtitle>Molecules (Basel, Switzerland)</jtitle><date>2021-09-06</date><risdate>2021</risdate><volume>26</volume><issue>17</issue><spage>5409</spage><pages>5409-</pages><issn>1420-3049</issn><eissn>1420-3049</eissn><abstract>Primary cilia mediate the interactions between cells and external stresses. Thus, dysregulation of primary cilia is implicated in various ciliopathies, e.g., degeneration of the retina caused by dysregulation of the photoreceptor primary cilium. Particulate matter (PM) can cause epithelium injury and endothelial dysfunction by increasing oxidative stress and inflammatory responses. Previously, we showed that PM disrupts the formation of primary cilia in retinal pigment epithelium (RPE) cells. In the present study, we identified 2-isopropylmalic acid (2-IPMA) as a novel inducer of primary ciliogenesis from a metabolite library screening. Both ciliated cells and primary cilium length were increased in 2-IPMA-treated RPE cells. Notably, 2-IPMA strongly promoted primary ciliogenesis and restored PM2.5-induced dysgenesis of primary cilia in RPE cells. Both excessive reactive oxygen species (ROS) generation and activation of a stress kinase, JNK, by PM2.5 were reduced by 2-IPMA. Moreover, 2-IPMA inhibited proinflammatory cytokine production, i.e., IL-6 and TNF-α, induced by PM2.5 in RPE cells. Taken together, our data suggest that 2-IPMA ameliorates PM2.5-induced inflammation by promoting primary ciliogenesis in RPE cells.</abstract><cop>Basel</cop><pub>MDPI AG</pub><pmid>34500843</pmid><doi>10.3390/molecules26175409</doi><orcidid>https://orcid.org/0000-0001-9319-5270</orcidid><orcidid>https://orcid.org/0000-0002-3837-9867</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 2-IPMA Air pollution Antibodies Apoptosis Cell culture Cell cycle Cilia Degeneration Epithelium Feces Gene expression Inflammation Interleukin 6 Libraries Metabolites Oxidative stress Particulate emissions Particulate matter particulate matter (PM2.5) primary cilia Proteins Reactive oxygen species Reagents Retina Retinal pigment epithelium RPE cells Signal transduction Software Stress measurement Tumor necrosis factor-α |
title | 2-IPMA Ameliorates PM2.5-Induced Inflammation by Promoting Primary Ciliogenesis in RPE Cells |
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