Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Molecules (Basel, Switzerland) Switzerland), 2021-09, Vol.26 (17), p.5409
Main Authors: 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
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c470t-d282520652d8c517919f05b3bbec21e006441113b54484d48a5d7b2a1ae5eaf83
cites cdi_FETCH-LOGICAL-c470t-d282520652d8c517919f05b3bbec21e006441113b54484d48a5d7b2a1ae5eaf83
container_end_page
container_issue 17
container_start_page 5409
container_title Molecules (Basel, Switzerland)
container_volume 26
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.
doi_str_mv 10.3390/molecules26175409
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_3e2945aa7b404759b9ed84be99ab13f7</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_3e2945aa7b404759b9ed84be99ab13f7</doaj_id><sourcerecordid>2571922583</sourcerecordid><originalsourceid>FETCH-LOGICAL-c470t-d282520652d8c517919f05b3bbec21e006441113b54484d48a5d7b2a1ae5eaf83</originalsourceid><addsrcrecordid>eNplkltrFEEQhRtRzMX8AN8afPFlYl93ul-EZYnJQIKL6Fug6UvN2stMd-yeEfLvM8kGMfpURdWpj8OhEHpPyTnnmnwa8wB-HqCyFW2lIPoVOqaCkYYToV__1R-hk1r3hDAqqHyLjriQhCjBj9Eta7rtzRqvRxhiLnaCirc37Fw2XQqzh4C71A92HO0Uc8LuHm9LHvMU027p4mjLPd7E5XQHCWqsOCb8bXuBNzAM9R1609uhwtlzPUU_vlx831w1118vu836uvGiJVMTmGKSkZVkQXlJW011T6TjzoFnFAhZCUEp5U4KoUQQysrQOmapBQm2V_wUdQduyHZv7g62TLbRPA1y2RlbpugHMByYFtLa1gkiWqmdhqCEA62to7xvF9bnA-tudiMED2kqdngBfblJ8afZ5d9miZNrJhfAx2dAyb9mqJMZY_VLHDZBnqthsqWaMan4Iv3wj3Sf55KWqJ5UgiuuHoH0oPIl11qg_2OGEvP4B-a_P-AP7PKk5Q</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2571438385</pqid></control><display><type>article</type><title>2-IPMA Ameliorates PM2.5-Induced Inflammation by Promoting Primary Ciliogenesis in RPE Cells</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>PubMed Central</source><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</creator><creatorcontrib>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</creatorcontrib><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><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 &amp; 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 &amp; Medical Complete (Alumni)</collection><collection>Health &amp; 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>
fulltext fulltext
identifier ISSN: 1420-3049
ispartof Molecules (Basel, Switzerland), 2021-09, Vol.26 (17), p.5409
issn 1420-3049
1420-3049
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_3e2945aa7b404759b9ed84be99ab13f7
source Publicly Available Content Database (Proquest) (PQ_SDU_P3); PubMed Central
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T15%3A54%3A27IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=2-IPMA%20Ameliorates%20PM2.5-Induced%20Inflammation%20by%20Promoting%20Primary%20Ciliogenesis%20in%20RPE%20Cells&rft.jtitle=Molecules%20(Basel,%20Switzerland)&rft.au=Choi,%20Ji%20Yeon&rft.date=2021-09-06&rft.volume=26&rft.issue=17&rft.spage=5409&rft.pages=5409-&rft.issn=1420-3049&rft.eissn=1420-3049&rft_id=info:doi/10.3390/molecules26175409&rft_dat=%3Cproquest_doaj_%3E2571922583%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c470t-d282520652d8c517919f05b3bbec21e006441113b54484d48a5d7b2a1ae5eaf83%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2571438385&rft_id=info:pmid/34500843&rfr_iscdi=true