Tweak/Fn14 system is involved in rhabdomyolysis-induced acute kidney injury
Rhabdomyolysis is a severe clinical syndrome associated to acute kidney injury (AKI) and chronic kidney disease (CKD). TWEAK/Fn14 signaling axis regulates renal inflammation and tubular cell death. However, the functional role of TWEAK/Fn14 in rhabdomyolysis remains unknown. Rhabdomyolysis was induc...
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Veröffentlicht in: | Biomedicine & pharmacotherapy 2023-12, Vol.169, p.115925-115925, Article 115925 |
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creator | Guerrero-Hue, Melania Vallejo-Mudarra, Mercedes García-Caballero, Cristina Córdoba-David, Gina Marcela Palomino-Antolín, Alejandra Herencia, Carmen Vendrell-Casana, Beatriz Rubio-Navarro, Alfonso Egido, Jesús Blanco-Colio, Luis Miguel Moreno, Juan Antonio |
description | Rhabdomyolysis is a severe clinical syndrome associated to acute kidney injury (AKI) and chronic kidney disease (CKD). TWEAK/Fn14 signaling axis regulates renal inflammation and tubular cell death. However, the functional role of TWEAK/Fn14 in rhabdomyolysis remains unknown.
Rhabdomyolysis was induced in wild-type, TWEAK- and Fn14-deficient mice or mice treated with TWEAK blocking antibody. Renal injury, inflammation, fibrosis and cell death were assessed. Additionally, we performed in vivo and in vitro studies to explore the possible signalling pathways involved in Fn14 regulation.
Fn14 renal expression was increased in mice with rhabdomyolysis, correlating with decline of renal function. Mechanistically, myoglobin (Mb) induced Fn14 expression via ERK and p38 pathway, whereas Nrf2 activation diminished Mb-mediated Fn14 upregulation in cultured renal cells. TWEAK or Fn14 genetic depletion ameliorated rhabdomyolysis-associated loss of renal function, histological damage, tubular cell death, inflammation, and expression of both tubular and endothelial injury markers. Deficiency of TWEAK or Fn14 also decreased long-term renal inflammation and fibrosis in mice with rhabdomyolysis. Finally, pharmacological treatment with a blocking TWEAK antibody diminished the expression of acute renal injury markers and cell death and lessened residual kidney fibrosis and chronic inflammation in rhabdomyolysis.
TWEAK/Fn14 axis participates in the pathogenesis of rhabdomyolysis-AKI and subsequent AKI-CKD transition. Blockade of this signaling pathway may represent a promising therapeutic strategy for reducing rhabdomyolysis-mediated renal injury.
Spanish Ministry of Science and Innovation, ISCIII and Junta de Andalucía.
[Display omitted]
•Rhabdomyolysis-derived myoglobin upregulates Fn14 expression in the kidney.•Genetic deletion of TWEAK or Fn14 reduces acute renal damage during rhabdomyolysis.•TWEAK/Fn14 axis participates in rhabdomyolysis-mediated fibrosis and inflammation.•Anti-TWEAK therapy reduces renal injury at early and late phases of rhabdomyolysis. |
doi_str_mv | 10.1016/j.biopha.2023.115925 |
format | Article |
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Rhabdomyolysis was induced in wild-type, TWEAK- and Fn14-deficient mice or mice treated with TWEAK blocking antibody. Renal injury, inflammation, fibrosis and cell death were assessed. Additionally, we performed in vivo and in vitro studies to explore the possible signalling pathways involved in Fn14 regulation.
Fn14 renal expression was increased in mice with rhabdomyolysis, correlating with decline of renal function. Mechanistically, myoglobin (Mb) induced Fn14 expression via ERK and p38 pathway, whereas Nrf2 activation diminished Mb-mediated Fn14 upregulation in cultured renal cells. TWEAK or Fn14 genetic depletion ameliorated rhabdomyolysis-associated loss of renal function, histological damage, tubular cell death, inflammation, and expression of both tubular and endothelial injury markers. Deficiency of TWEAK or Fn14 also decreased long-term renal inflammation and fibrosis in mice with rhabdomyolysis. Finally, pharmacological treatment with a blocking TWEAK antibody diminished the expression of acute renal injury markers and cell death and lessened residual kidney fibrosis and chronic inflammation in rhabdomyolysis.
TWEAK/Fn14 axis participates in the pathogenesis of rhabdomyolysis-AKI and subsequent AKI-CKD transition. Blockade of this signaling pathway may represent a promising therapeutic strategy for reducing rhabdomyolysis-mediated renal injury.
Spanish Ministry of Science and Innovation, ISCIII and Junta de Andalucía.
[Display omitted]
•Rhabdomyolysis-derived myoglobin upregulates Fn14 expression in the kidney.•Genetic deletion of TWEAK or Fn14 reduces acute renal damage during rhabdomyolysis.•TWEAK/Fn14 axis participates in rhabdomyolysis-mediated fibrosis and inflammation.•Anti-TWEAK therapy reduces renal injury at early and late phases of rhabdomyolysis.</description><identifier>ISSN: 0753-3322</identifier><identifier>EISSN: 1950-6007</identifier><identifier>DOI: 10.1016/j.biopha.2023.115925</identifier><identifier>PMID: 38007933</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Acute kidney injury ; Acute Kidney Injury - metabolism ; Animals ; Cytokine TWEAK - metabolism ; Fibrosis ; Fn14 ; Inflammation ; Mice ; Myoglobin ; Renal Insufficiency, Chronic ; Rhabdomyolysis ; Rhabdomyolysis - complications ; Tumor Necrosis Factors - metabolism ; TWEAK ; TWEAK Receptor - metabolism</subject><ispartof>Biomedicine & pharmacotherapy, 2023-12, Vol.169, p.115925-115925, Article 115925</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. Published by Elsevier Masson SAS.. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c357t-6e8c3579c2856aca12d83ddfcfccaeda00eecbafcaa3e0740fb84badd2192ef53</cites><orcidid>0000-0002-7468-2871 ; 0000-0002-5922-6261</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.biopha.2023.115925$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38007933$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Guerrero-Hue, Melania</creatorcontrib><creatorcontrib>Vallejo-Mudarra, Mercedes</creatorcontrib><creatorcontrib>García-Caballero, Cristina</creatorcontrib><creatorcontrib>Córdoba-David, Gina Marcela</creatorcontrib><creatorcontrib>Palomino-Antolín, Alejandra</creatorcontrib><creatorcontrib>Herencia, Carmen</creatorcontrib><creatorcontrib>Vendrell-Casana, Beatriz</creatorcontrib><creatorcontrib>Rubio-Navarro, Alfonso</creatorcontrib><creatorcontrib>Egido, Jesús</creatorcontrib><creatorcontrib>Blanco-Colio, Luis Miguel</creatorcontrib><creatorcontrib>Moreno, Juan Antonio</creatorcontrib><title>Tweak/Fn14 system is involved in rhabdomyolysis-induced acute kidney injury</title><title>Biomedicine & pharmacotherapy</title><addtitle>Biomed Pharmacother</addtitle><description>Rhabdomyolysis is a severe clinical syndrome associated to acute kidney injury (AKI) and chronic kidney disease (CKD). TWEAK/Fn14 signaling axis regulates renal inflammation and tubular cell death. However, the functional role of TWEAK/Fn14 in rhabdomyolysis remains unknown.
Rhabdomyolysis was induced in wild-type, TWEAK- and Fn14-deficient mice or mice treated with TWEAK blocking antibody. Renal injury, inflammation, fibrosis and cell death were assessed. Additionally, we performed in vivo and in vitro studies to explore the possible signalling pathways involved in Fn14 regulation.
Fn14 renal expression was increased in mice with rhabdomyolysis, correlating with decline of renal function. Mechanistically, myoglobin (Mb) induced Fn14 expression via ERK and p38 pathway, whereas Nrf2 activation diminished Mb-mediated Fn14 upregulation in cultured renal cells. TWEAK or Fn14 genetic depletion ameliorated rhabdomyolysis-associated loss of renal function, histological damage, tubular cell death, inflammation, and expression of both tubular and endothelial injury markers. Deficiency of TWEAK or Fn14 also decreased long-term renal inflammation and fibrosis in mice with rhabdomyolysis. Finally, pharmacological treatment with a blocking TWEAK antibody diminished the expression of acute renal injury markers and cell death and lessened residual kidney fibrosis and chronic inflammation in rhabdomyolysis.
TWEAK/Fn14 axis participates in the pathogenesis of rhabdomyolysis-AKI and subsequent AKI-CKD transition. Blockade of this signaling pathway may represent a promising therapeutic strategy for reducing rhabdomyolysis-mediated renal injury.
Spanish Ministry of Science and Innovation, ISCIII and Junta de Andalucía.
[Display omitted]
•Rhabdomyolysis-derived myoglobin upregulates Fn14 expression in the kidney.•Genetic deletion of TWEAK or Fn14 reduces acute renal damage during rhabdomyolysis.•TWEAK/Fn14 axis participates in rhabdomyolysis-mediated fibrosis and inflammation.•Anti-TWEAK therapy reduces renal injury at early and late phases of rhabdomyolysis.</description><subject>Acute kidney injury</subject><subject>Acute Kidney Injury - metabolism</subject><subject>Animals</subject><subject>Cytokine TWEAK - metabolism</subject><subject>Fibrosis</subject><subject>Fn14</subject><subject>Inflammation</subject><subject>Mice</subject><subject>Myoglobin</subject><subject>Renal Insufficiency, Chronic</subject><subject>Rhabdomyolysis</subject><subject>Rhabdomyolysis - complications</subject><subject>Tumor Necrosis Factors - metabolism</subject><subject>TWEAK</subject><subject>TWEAK Receptor - metabolism</subject><issn>0753-3322</issn><issn>1950-6007</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtOwzAQRS0EoqXwBwhlySapH3EeGySEKCAqsSlry7EnqtM8ip0U5e9xlcKS1VxpzsxoDkK3BEcEk2RZRYXp9lsZUUxZRAjPKT9Dc5JzHCYYp-dojlPOQsYonaEr5yqMMU9YdolmLPNAztgcvW--Qe6Wq5bEgRtdD01gXGDaQ1cfQPsQ2K0sdNeMXT0640LT6kH5jlRDD8HO6BZGj1WDHa_RRSlrBzenukCfq-fN02u4_nh5e3pch4rxtA8TyI4hVzTjiVSSUJ0xrUtVKiVBS4wBVCFLJSUDnMa4LLK4kFpTklMoOVug-2nv3nZfA7heNMYpqGvZQjc4QbM8ZgnFhHg0nlBlO-cslGJvTSPtKAgWR42iEpNGcdQoJo1-7O50YSga0H9Dv9488DAB4P88GLDCKQOtF2MsqF7ozvx_4Qf6vYcu</recordid><startdate>20231231</startdate><enddate>20231231</enddate><creator>Guerrero-Hue, Melania</creator><creator>Vallejo-Mudarra, Mercedes</creator><creator>García-Caballero, Cristina</creator><creator>Córdoba-David, Gina Marcela</creator><creator>Palomino-Antolín, Alejandra</creator><creator>Herencia, Carmen</creator><creator>Vendrell-Casana, Beatriz</creator><creator>Rubio-Navarro, Alfonso</creator><creator>Egido, Jesús</creator><creator>Blanco-Colio, Luis Miguel</creator><creator>Moreno, Juan Antonio</creator><general>Elsevier Masson SAS</general><scope>6I.</scope><scope>AAFTH</scope><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>7X8</scope><orcidid>https://orcid.org/0000-0002-7468-2871</orcidid><orcidid>https://orcid.org/0000-0002-5922-6261</orcidid></search><sort><creationdate>20231231</creationdate><title>Tweak/Fn14 system is involved in rhabdomyolysis-induced acute kidney injury</title><author>Guerrero-Hue, Melania ; Vallejo-Mudarra, Mercedes ; García-Caballero, Cristina ; Córdoba-David, Gina Marcela ; Palomino-Antolín, Alejandra ; Herencia, Carmen ; Vendrell-Casana, Beatriz ; Rubio-Navarro, Alfonso ; Egido, Jesús ; Blanco-Colio, Luis Miguel ; Moreno, Juan Antonio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c357t-6e8c3579c2856aca12d83ddfcfccaeda00eecbafcaa3e0740fb84badd2192ef53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Acute kidney injury</topic><topic>Acute Kidney Injury - metabolism</topic><topic>Animals</topic><topic>Cytokine TWEAK - metabolism</topic><topic>Fibrosis</topic><topic>Fn14</topic><topic>Inflammation</topic><topic>Mice</topic><topic>Myoglobin</topic><topic>Renal Insufficiency, Chronic</topic><topic>Rhabdomyolysis</topic><topic>Rhabdomyolysis - complications</topic><topic>Tumor Necrosis Factors - metabolism</topic><topic>TWEAK</topic><topic>TWEAK Receptor - metabolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Guerrero-Hue, Melania</creatorcontrib><creatorcontrib>Vallejo-Mudarra, Mercedes</creatorcontrib><creatorcontrib>García-Caballero, Cristina</creatorcontrib><creatorcontrib>Córdoba-David, Gina Marcela</creatorcontrib><creatorcontrib>Palomino-Antolín, Alejandra</creatorcontrib><creatorcontrib>Herencia, Carmen</creatorcontrib><creatorcontrib>Vendrell-Casana, Beatriz</creatorcontrib><creatorcontrib>Rubio-Navarro, Alfonso</creatorcontrib><creatorcontrib>Egido, Jesús</creatorcontrib><creatorcontrib>Blanco-Colio, Luis Miguel</creatorcontrib><creatorcontrib>Moreno, Juan Antonio</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biomedicine & pharmacotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Guerrero-Hue, Melania</au><au>Vallejo-Mudarra, Mercedes</au><au>García-Caballero, Cristina</au><au>Córdoba-David, Gina Marcela</au><au>Palomino-Antolín, Alejandra</au><au>Herencia, Carmen</au><au>Vendrell-Casana, Beatriz</au><au>Rubio-Navarro, Alfonso</au><au>Egido, Jesús</au><au>Blanco-Colio, Luis Miguel</au><au>Moreno, Juan Antonio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tweak/Fn14 system is involved in rhabdomyolysis-induced acute kidney injury</atitle><jtitle>Biomedicine & pharmacotherapy</jtitle><addtitle>Biomed Pharmacother</addtitle><date>2023-12-31</date><risdate>2023</risdate><volume>169</volume><spage>115925</spage><epage>115925</epage><pages>115925-115925</pages><artnum>115925</artnum><issn>0753-3322</issn><eissn>1950-6007</eissn><abstract>Rhabdomyolysis is a severe clinical syndrome associated to acute kidney injury (AKI) and chronic kidney disease (CKD). TWEAK/Fn14 signaling axis regulates renal inflammation and tubular cell death. However, the functional role of TWEAK/Fn14 in rhabdomyolysis remains unknown.
Rhabdomyolysis was induced in wild-type, TWEAK- and Fn14-deficient mice or mice treated with TWEAK blocking antibody. Renal injury, inflammation, fibrosis and cell death were assessed. Additionally, we performed in vivo and in vitro studies to explore the possible signalling pathways involved in Fn14 regulation.
Fn14 renal expression was increased in mice with rhabdomyolysis, correlating with decline of renal function. Mechanistically, myoglobin (Mb) induced Fn14 expression via ERK and p38 pathway, whereas Nrf2 activation diminished Mb-mediated Fn14 upregulation in cultured renal cells. TWEAK or Fn14 genetic depletion ameliorated rhabdomyolysis-associated loss of renal function, histological damage, tubular cell death, inflammation, and expression of both tubular and endothelial injury markers. Deficiency of TWEAK or Fn14 also decreased long-term renal inflammation and fibrosis in mice with rhabdomyolysis. Finally, pharmacological treatment with a blocking TWEAK antibody diminished the expression of acute renal injury markers and cell death and lessened residual kidney fibrosis and chronic inflammation in rhabdomyolysis.
TWEAK/Fn14 axis participates in the pathogenesis of rhabdomyolysis-AKI and subsequent AKI-CKD transition. Blockade of this signaling pathway may represent a promising therapeutic strategy for reducing rhabdomyolysis-mediated renal injury.
Spanish Ministry of Science and Innovation, ISCIII and Junta de Andalucía.
[Display omitted]
•Rhabdomyolysis-derived myoglobin upregulates Fn14 expression in the kidney.•Genetic deletion of TWEAK or Fn14 reduces acute renal damage during rhabdomyolysis.•TWEAK/Fn14 axis participates in rhabdomyolysis-mediated fibrosis and inflammation.•Anti-TWEAK therapy reduces renal injury at early and late phases of rhabdomyolysis.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>38007933</pmid><doi>10.1016/j.biopha.2023.115925</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-7468-2871</orcidid><orcidid>https://orcid.org/0000-0002-5922-6261</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Acute kidney injury Acute Kidney Injury - metabolism Animals Cytokine TWEAK - metabolism Fibrosis Fn14 Inflammation Mice Myoglobin Renal Insufficiency, Chronic Rhabdomyolysis Rhabdomyolysis - complications Tumor Necrosis Factors - metabolism TWEAK TWEAK Receptor - metabolism |
title | Tweak/Fn14 system is involved in rhabdomyolysis-induced acute kidney injury |
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