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
Hauptverfasser: 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
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container_title Biomedicine & pharmacotherapy
container_volume 169
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
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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><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 &amp; pharmacotherapy, 2023-12, Vol.169, p.115925-115925, Article 115925</ispartof><rights>2023 The Authors</rights><rights>Copyright © 2023 The Authors. 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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 ; 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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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