Microplastics exposure induced and exacerbated the development of systemic lupus erythematosus in mice

Environmental exposure may function as a contributing risk factor in the development of systemic lupus erythematosus (SLE). Recently, the global issue of microplastics (MPs) pollution has garnered increasing concern, yet its potential impact on SLE remains unexplored. This study seeks to elucidate t...

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Veröffentlicht in:The Science of the total environment 2024-01, Vol.909, p.168586-168586, Article 168586
Hauptverfasser: Chen, Huinan, Wan, Li, Qiu, Yiwu, Qiu, Fuhai, Wen, Chengping, Mao, Yingying, He, Zhixing
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container_title The Science of the total environment
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Wan, Li
Qiu, Yiwu
Qiu, Fuhai
Wen, Chengping
Mao, Yingying
He, Zhixing
description Environmental exposure may function as a contributing risk factor in the development of systemic lupus erythematosus (SLE). Recently, the global issue of microplastics (MPs) pollution has garnered increasing concern, yet its potential impact on SLE remains unexplored. This study seeks to elucidate the ramifications of MPs exposure on lupus manifestations in spontaneous lupus MRL/lpr mice and normal C57L/6 mice. MPs exposure demonstrated the capacity to induce lupus-like symptoms in C57BL/6 mice and exacerbate lupus symptoms in MRL/lpr mice. This was manifested by MPs triggering abnormal elevation of spleen DN T, plasma cells, serum anti-dsDNA, ANA, IL-6, and TNF-α, coupled with a reduction in spleen CD4+/CD8+ cell ratio, and impairment in renal pathology. Moreover, a 4D-DIA quantitative proteomic analysis was employed to unveil substantial alterations in renal proteins attributed to MPs exposure. The findings indicated that the KEGG pathways significantly enriched by MPs-associated different proteins in C57BL/6 mice were closely aligned with the enriched KEGG pathways associated with lupus. Unlike C57BL/6 mice, there were no significantly enriched KEGG pathways identified among the MPs-associated different proteins in MRL/lpr mice. In addition, proteins related to the SLE pathway illuminated that MPs exposure induced renal damage through activation of MHCII and histone H3, culminating in the production of MAC in both C57BL/6 and MRL/lpr mice. However, a specific elevation in cathepsin and elastase caused by MPs was observed in C57BL/6 mice but not in MRL/lpr mice. This study represents a significant stride in bridging the existing knowledge gap pertaining to the intricate relationship between MPs exposure and the development of SLE. [Display omitted] •Effects of microplastics (MPs) was studied in spontaneous lupus-prone MRL/lpr mice and normal C57BL/6 mice.•MPs exposure exacerbated lupus symptoms in MRL/lpr mice.•MPs exposure induced lupus-like symptoms in C57BL/6 mice.•Proteomics analysis underscored the similarity between MPs-induced kidney damage and the kidney damage resulting from lupus.
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Recently, the global issue of microplastics (MPs) pollution has garnered increasing concern, yet its potential impact on SLE remains unexplored. This study seeks to elucidate the ramifications of MPs exposure on lupus manifestations in spontaneous lupus MRL/lpr mice and normal C57L/6 mice. MPs exposure demonstrated the capacity to induce lupus-like symptoms in C57BL/6 mice and exacerbate lupus symptoms in MRL/lpr mice. This was manifested by MPs triggering abnormal elevation of spleen DN T, plasma cells, serum anti-dsDNA, ANA, IL-6, and TNF-α, coupled with a reduction in spleen CD4+/CD8+ cell ratio, and impairment in renal pathology. Moreover, a 4D-DIA quantitative proteomic analysis was employed to unveil substantial alterations in renal proteins attributed to MPs exposure. The findings indicated that the KEGG pathways significantly enriched by MPs-associated different proteins in C57BL/6 mice were closely aligned with the enriched KEGG pathways associated with lupus. Unlike C57BL/6 mice, there were no significantly enriched KEGG pathways identified among the MPs-associated different proteins in MRL/lpr mice. In addition, proteins related to the SLE pathway illuminated that MPs exposure induced renal damage through activation of MHCII and histone H3, culminating in the production of MAC in both C57BL/6 and MRL/lpr mice. However, a specific elevation in cathepsin and elastase caused by MPs was observed in C57BL/6 mice but not in MRL/lpr mice. This study represents a significant stride in bridging the existing knowledge gap pertaining to the intricate relationship between MPs exposure and the development of SLE. [Display omitted] •Effects of microplastics (MPs) was studied in spontaneous lupus-prone MRL/lpr mice and normal C57BL/6 mice.•MPs exposure exacerbated lupus symptoms in MRL/lpr mice.•MPs exposure induced lupus-like symptoms in C57BL/6 mice.•Proteomics analysis underscored the similarity between MPs-induced kidney damage and the kidney damage resulting from lupus.</description><identifier>ISSN: 0048-9697</identifier><identifier>EISSN: 1879-1026</identifier><identifier>DOI: 10.1016/j.scitotenv.2023.168586</identifier><language>eng</language><publisher>Elsevier B.V</publisher><subject>blood serum ; cathepsins ; elastase ; environment ; environmental exposure ; histones ; interleukin-6 ; lupus erythematosus ; Microplastics ; MRL/lpr mice ; pollution ; proteomics ; Renal injury ; Renal proteomics ; risk factors ; spleen ; Systemic lupus erythematosus</subject><ispartof>The Science of the total environment, 2024-01, Vol.909, p.168586-168586, Article 168586</ispartof><rights>2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-de0fae6d0e4b7cd7283bf7cc5e604d1650a2070364637f1da217f2f91c2593aa3</citedby><cites>FETCH-LOGICAL-c381t-de0fae6d0e4b7cd7283bf7cc5e604d1650a2070364637f1da217f2f91c2593aa3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.scitotenv.2023.168586$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,778,782,3539,27911,27912,45982</link.rule.ids></links><search><creatorcontrib>Chen, Huinan</creatorcontrib><creatorcontrib>Wan, Li</creatorcontrib><creatorcontrib>Qiu, Yiwu</creatorcontrib><creatorcontrib>Qiu, Fuhai</creatorcontrib><creatorcontrib>Wen, Chengping</creatorcontrib><creatorcontrib>Mao, Yingying</creatorcontrib><creatorcontrib>He, Zhixing</creatorcontrib><title>Microplastics exposure induced and exacerbated the development of systemic lupus erythematosus in mice</title><title>The Science of the total environment</title><description>Environmental exposure may function as a contributing risk factor in the development of systemic lupus erythematosus (SLE). Recently, the global issue of microplastics (MPs) pollution has garnered increasing concern, yet its potential impact on SLE remains unexplored. This study seeks to elucidate the ramifications of MPs exposure on lupus manifestations in spontaneous lupus MRL/lpr mice and normal C57L/6 mice. MPs exposure demonstrated the capacity to induce lupus-like symptoms in C57BL/6 mice and exacerbate lupus symptoms in MRL/lpr mice. This was manifested by MPs triggering abnormal elevation of spleen DN T, plasma cells, serum anti-dsDNA, ANA, IL-6, and TNF-α, coupled with a reduction in spleen CD4+/CD8+ cell ratio, and impairment in renal pathology. Moreover, a 4D-DIA quantitative proteomic analysis was employed to unveil substantial alterations in renal proteins attributed to MPs exposure. The findings indicated that the KEGG pathways significantly enriched by MPs-associated different proteins in C57BL/6 mice were closely aligned with the enriched KEGG pathways associated with lupus. Unlike C57BL/6 mice, there were no significantly enriched KEGG pathways identified among the MPs-associated different proteins in MRL/lpr mice. In addition, proteins related to the SLE pathway illuminated that MPs exposure induced renal damage through activation of MHCII and histone H3, culminating in the production of MAC in both C57BL/6 and MRL/lpr mice. However, a specific elevation in cathepsin and elastase caused by MPs was observed in C57BL/6 mice but not in MRL/lpr mice. This study represents a significant stride in bridging the existing knowledge gap pertaining to the intricate relationship between MPs exposure and the development of SLE. [Display omitted] •Effects of microplastics (MPs) was studied in spontaneous lupus-prone MRL/lpr mice and normal C57BL/6 mice.•MPs exposure exacerbated lupus symptoms in MRL/lpr mice.•MPs exposure induced lupus-like symptoms in C57BL/6 mice.•Proteomics analysis underscored the similarity between MPs-induced kidney damage and the kidney damage resulting from lupus.</description><subject>blood serum</subject><subject>cathepsins</subject><subject>elastase</subject><subject>environment</subject><subject>environmental exposure</subject><subject>histones</subject><subject>interleukin-6</subject><subject>lupus erythematosus</subject><subject>Microplastics</subject><subject>MRL/lpr mice</subject><subject>pollution</subject><subject>proteomics</subject><subject>Renal injury</subject><subject>Renal proteomics</subject><subject>risk factors</subject><subject>spleen</subject><subject>Systemic lupus erythematosus</subject><issn>0048-9697</issn><issn>1879-1026</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkU1PAyEQhonRxPrxG9yjl60D7MLusWn8SjRe9EwoDJFmvwS2sf9emhqvcpnAPPMkzEvIDYUlBSrutstofBoTDrslA8aXVDR1I07IgjayLSkwcUoWAFVTtqKV5-Qixi3kIxu6IO7VmzBOnY7Jm1jg9zTGOWDhBzsbtIUebH7UBsNGp3xPn1hY3GE3Tj0OqRhdEfcxYe9N0c3TnBVhn6FepyyK2VPkFl6RM6e7iNe_9ZJ8PNy_r5_Kl7fH5_XqpTS8oam0CE6jsIDVRhorWcM3ThpTo4DKUlGDZiCBi0pw6ajVjErHXEsNq1uuNb8kt0fvFMavGWNSvY8Gu04POM5RcVpzCSAY_RdlTcuAskqKjMojmlcVY0CnpuB7HfaKgjqEoLbqLwR1CEEdQ8iTq-Mk5k_vPIYDh0PerA9okrKj_9fxAy1tlwA</recordid><startdate>20240120</startdate><enddate>20240120</enddate><creator>Chen, Huinan</creator><creator>Wan, Li</creator><creator>Qiu, Yiwu</creator><creator>Qiu, Fuhai</creator><creator>Wen, Chengping</creator><creator>Mao, Yingying</creator><creator>He, Zhixing</creator><general>Elsevier B.V</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20240120</creationdate><title>Microplastics exposure induced and exacerbated the development of systemic lupus erythematosus in mice</title><author>Chen, Huinan ; Wan, Li ; Qiu, Yiwu ; Qiu, Fuhai ; Wen, Chengping ; Mao, Yingying ; He, Zhixing</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c381t-de0fae6d0e4b7cd7283bf7cc5e604d1650a2070364637f1da217f2f91c2593aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>blood serum</topic><topic>cathepsins</topic><topic>elastase</topic><topic>environment</topic><topic>environmental exposure</topic><topic>histones</topic><topic>interleukin-6</topic><topic>lupus erythematosus</topic><topic>Microplastics</topic><topic>MRL/lpr mice</topic><topic>pollution</topic><topic>proteomics</topic><topic>Renal injury</topic><topic>Renal proteomics</topic><topic>risk factors</topic><topic>spleen</topic><topic>Systemic lupus erythematosus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chen, Huinan</creatorcontrib><creatorcontrib>Wan, Li</creatorcontrib><creatorcontrib>Qiu, Yiwu</creatorcontrib><creatorcontrib>Qiu, Fuhai</creatorcontrib><creatorcontrib>Wen, Chengping</creatorcontrib><creatorcontrib>Mao, Yingying</creatorcontrib><creatorcontrib>He, Zhixing</creatorcontrib><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>The Science of the total environment</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chen, Huinan</au><au>Wan, Li</au><au>Qiu, Yiwu</au><au>Qiu, Fuhai</au><au>Wen, Chengping</au><au>Mao, Yingying</au><au>He, Zhixing</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microplastics exposure induced and exacerbated the development of systemic lupus erythematosus in mice</atitle><jtitle>The Science of the total environment</jtitle><date>2024-01-20</date><risdate>2024</risdate><volume>909</volume><spage>168586</spage><epage>168586</epage><pages>168586-168586</pages><artnum>168586</artnum><issn>0048-9697</issn><eissn>1879-1026</eissn><abstract>Environmental exposure may function as a contributing risk factor in the development of systemic lupus erythematosus (SLE). Recently, the global issue of microplastics (MPs) pollution has garnered increasing concern, yet its potential impact on SLE remains unexplored. This study seeks to elucidate the ramifications of MPs exposure on lupus manifestations in spontaneous lupus MRL/lpr mice and normal C57L/6 mice. MPs exposure demonstrated the capacity to induce lupus-like symptoms in C57BL/6 mice and exacerbate lupus symptoms in MRL/lpr mice. This was manifested by MPs triggering abnormal elevation of spleen DN T, plasma cells, serum anti-dsDNA, ANA, IL-6, and TNF-α, coupled with a reduction in spleen CD4+/CD8+ cell ratio, and impairment in renal pathology. Moreover, a 4D-DIA quantitative proteomic analysis was employed to unveil substantial alterations in renal proteins attributed to MPs exposure. The findings indicated that the KEGG pathways significantly enriched by MPs-associated different proteins in C57BL/6 mice were closely aligned with the enriched KEGG pathways associated with lupus. Unlike C57BL/6 mice, there were no significantly enriched KEGG pathways identified among the MPs-associated different proteins in MRL/lpr mice. In addition, proteins related to the SLE pathway illuminated that MPs exposure induced renal damage through activation of MHCII and histone H3, culminating in the production of MAC in both C57BL/6 and MRL/lpr mice. However, a specific elevation in cathepsin and elastase caused by MPs was observed in C57BL/6 mice but not in MRL/lpr mice. This study represents a significant stride in bridging the existing knowledge gap pertaining to the intricate relationship between MPs exposure and the development of SLE. [Display omitted] •Effects of microplastics (MPs) was studied in spontaneous lupus-prone MRL/lpr mice and normal C57BL/6 mice.•MPs exposure exacerbated lupus symptoms in MRL/lpr mice.•MPs exposure induced lupus-like symptoms in C57BL/6 mice.•Proteomics analysis underscored the similarity between MPs-induced kidney damage and the kidney damage resulting from lupus.</abstract><pub>Elsevier B.V</pub><doi>10.1016/j.scitotenv.2023.168586</doi><tpages>1</tpages></addata></record>
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subjects blood serum
cathepsins
elastase
environment
environmental exposure
histones
interleukin-6
lupus erythematosus
Microplastics
MRL/lpr mice
pollution
proteomics
Renal injury
Renal proteomics
risk factors
spleen
Systemic lupus erythematosus
title Microplastics exposure induced and exacerbated the development of systemic lupus erythematosus in mice
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