Knockout of Erbin promotes pyroptosis via regulating NLRP3/caspase-1/Gasdermin D pathway in sepsis-induced acute kidney injury

Background This study aims to investigate the correlation between Erbin and sepsis, and the role of Erbin on the pyroptosis pathway in acute kidney injury caused by sepsis and NLRP3/caspase-1/Gasdermin D pathway. Methods In the study, lipopolysaccharide (LPS) treatment or cecal ligation and puncture...

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Veröffentlicht in:Clinical and experimental nephrology 2023-09, Vol.27 (9), p.781-790
Hauptverfasser: Liu, Yuping, Fang, Qing, Ming, Tingqian, Zuo, Jing, Jing, Guoqing, Song, Xuemin
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container_issue 9
container_start_page 781
container_title Clinical and experimental nephrology
container_volume 27
creator Liu, Yuping
Fang, Qing
Ming, Tingqian
Zuo, Jing
Jing, Guoqing
Song, Xuemin
description Background This study aims to investigate the correlation between Erbin and sepsis, and the role of Erbin on the pyroptosis pathway in acute kidney injury caused by sepsis and NLRP3/caspase-1/Gasdermin D pathway. Methods In the study, lipopolysaccharide (LPS) treatment or cecal ligation and puncture (CLP) surgery on mice were used to stimulate the in vitro and in vivo sepsis-induced renal injury model. The male C57BL/6 of wild-type mice (WT) and Erbin-knockout mice (Erbin −/− , EKO) were randomly divided into four groups (WT + Sham, WT + CLP, EKO + Sham, EKO + CLP). Inflammatory cytokine, renal function, pyroptotic cell numbers and the levels of protein and mRNA expression of pyroptosis, including the NLRP3 (all P  
doi_str_mv 10.1007/s10157-023-02364-8
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Methods In the study, lipopolysaccharide (LPS) treatment or cecal ligation and puncture (CLP) surgery on mice were used to stimulate the in vitro and in vivo sepsis-induced renal injury model. The male C57BL/6 of wild-type mice (WT) and Erbin-knockout mice (Erbin −/− , EKO) were randomly divided into four groups (WT + Sham, WT + CLP, EKO + Sham, EKO + CLP). Inflammatory cytokine, renal function, pyroptotic cell numbers and the levels of protein and mRNA expression of pyroptosis, including the NLRP3 (all P  &lt; 0.05), were analyzed and found increase in Erbin −/− mice with CLP and LPS-induced HK-2 cells. Results The inhibited of Erbin shows a renal damaged effect by promoting NLRP3 inflammasome-mediated pyroptosis in SI-AKI. Conclusion This study demonstrated a novel mechanism by which Erbin regulates NLRP3 inflammasome-mediated pyroptosis in SI-AKI.</description><identifier>ISSN: 1342-1751</identifier><identifier>EISSN: 1437-7799</identifier><identifier>DOI: 10.1007/s10157-023-02364-8</identifier><identifier>PMID: 37310569</identifier><language>eng</language><publisher>Singapore: Springer Nature Singapore</publisher><subject>Caspase-1 ; Cecum ; Gene expression ; Inflammasomes ; Inflammation ; Kidneys ; Lipopolysaccharides ; Medicine ; Medicine &amp; Public Health ; Nephrology ; Original Article ; Pyroptosis ; Renal function ; Sepsis ; Urology</subject><ispartof>Clinical and experimental nephrology, 2023-09, Vol.27 (9), p.781-790</ispartof><rights>The Author(s), under exclusive licence to The Japanese Society of Nephrology 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to The Japanese Society of Nephrology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c350t-7c35c4a6222f7fdb2114853ab3ff70ff106a24c62f37988ed31c615a2f2000b33</cites><orcidid>0000-0002-1887-8386</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10157-023-02364-8$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10157-023-02364-8$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37310569$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Yuping</creatorcontrib><creatorcontrib>Fang, Qing</creatorcontrib><creatorcontrib>Ming, Tingqian</creatorcontrib><creatorcontrib>Zuo, Jing</creatorcontrib><creatorcontrib>Jing, Guoqing</creatorcontrib><creatorcontrib>Song, Xuemin</creatorcontrib><title>Knockout of Erbin promotes pyroptosis via regulating NLRP3/caspase-1/Gasdermin D pathway in sepsis-induced acute kidney injury</title><title>Clinical and experimental nephrology</title><addtitle>Clin Exp Nephrol</addtitle><addtitle>Clin Exp Nephrol</addtitle><description>Background This study aims to investigate the correlation between Erbin and sepsis, and the role of Erbin on the pyroptosis pathway in acute kidney injury caused by sepsis and NLRP3/caspase-1/Gasdermin D pathway. Methods In the study, lipopolysaccharide (LPS) treatment or cecal ligation and puncture (CLP) surgery on mice were used to stimulate the in vitro and in vivo sepsis-induced renal injury model. The male C57BL/6 of wild-type mice (WT) and Erbin-knockout mice (Erbin −/− , EKO) were randomly divided into four groups (WT + Sham, WT + CLP, EKO + Sham, EKO + CLP). Inflammatory cytokine, renal function, pyroptotic cell numbers and the levels of protein and mRNA expression of pyroptosis, including the NLRP3 (all P  &lt; 0.05), were analyzed and found increase in Erbin −/− mice with CLP and LPS-induced HK-2 cells. Results The inhibited of Erbin shows a renal damaged effect by promoting NLRP3 inflammasome-mediated pyroptosis in SI-AKI. Conclusion This study demonstrated a novel mechanism by which Erbin regulates NLRP3 inflammasome-mediated pyroptosis in SI-AKI.</description><subject>Caspase-1</subject><subject>Cecum</subject><subject>Gene expression</subject><subject>Inflammasomes</subject><subject>Inflammation</subject><subject>Kidneys</subject><subject>Lipopolysaccharides</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Nephrology</subject><subject>Original Article</subject><subject>Pyroptosis</subject><subject>Renal function</subject><subject>Sepsis</subject><subject>Urology</subject><issn>1342-1751</issn><issn>1437-7799</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>BENPR</sourceid><recordid>eNp9kU9v1DAQxa2KipbCF-gBWeLCxaz_xLFzrEppK1YtQnC2HMdest3EwROD9sJnr5ctrcShB2tsze-98eghdMroB0apWgCjTCpCudiduiL6AB2zSiiiVNO8KHdRccKUZEfoFcCaUqob2bxER0IJRmXdHKM_n8fo7mKecQz4IrX9iKcUhzh7wNM2xWmO0AP-1Vuc_Cpv7NyPK3yz_PpFLJyFyYInbHFpofNpKOKPeLLzj992i8sD_FTEpB-77HyHrcuzx3d9N_pde53T9jU6DHYD_s1DPUHfP118O78iy9vL6_OzJXFC0pmoUlxla855UKFrOWOVlsK2IgRFQ2C0trxyNQ9CNVr7TjBXM2l54GXpVogT9H7vW5b7mT3MZujB-c3Gjj5mMFxzKSmvuC7ou__QdcxpLL8rVEOF0Jo2heJ7yqUIkHwwU-oHm7aGUbNLx-zTMSUZ8zcds7N--2Cd28F3j5J_cRRA7AEorXHl09PsZ2zvAaDSmqw</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Liu, Yuping</creator><creator>Fang, Qing</creator><creator>Ming, Tingqian</creator><creator>Zuo, Jing</creator><creator>Jing, Guoqing</creator><creator>Song, Xuemin</creator><general>Springer Nature Singapore</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-1887-8386</orcidid></search><sort><creationdate>20230901</creationdate><title>Knockout of Erbin promotes pyroptosis via regulating NLRP3/caspase-1/Gasdermin D pathway in sepsis-induced acute kidney injury</title><author>Liu, Yuping ; 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Conclusion This study demonstrated a novel mechanism by which Erbin regulates NLRP3 inflammasome-mediated pyroptosis in SI-AKI.</abstract><cop>Singapore</cop><pub>Springer Nature Singapore</pub><pmid>37310569</pmid><doi>10.1007/s10157-023-02364-8</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0002-1887-8386</orcidid></addata></record>
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subjects Caspase-1
Cecum
Gene expression
Inflammasomes
Inflammation
Kidneys
Lipopolysaccharides
Medicine
Medicine & Public Health
Nephrology
Original Article
Pyroptosis
Renal function
Sepsis
Urology
title Knockout of Erbin promotes pyroptosis via regulating NLRP3/caspase-1/Gasdermin D pathway in sepsis-induced acute kidney injury
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