Acute kidney injury transcriptomics unveils a relationship between inflammation and ageing

There are no pathophysiolgical therapeutic approaches to acute kidney injury (AKI) and the mortality remains high. In addition chronic kidney disease (CKD) predisposes to AKI and AKI contributes to progression of CKD. Recently a transcriptomics approach unveiled a relationship between AKI, inflammation and the regulation of ageing. A transcriptomics analysis of experimental AKI revealed increased kidney expression of Fn14 and transmembrane chemokine CXCL16, as well as a decreased expression of the kidney-secreted anti-ageing hormone Klotho. Fn14 is the receptor for tumor necrosis factor-like weak inducer of apoptosis (TWEAK), a member of the TNF superfamily. In AKI kidneys there was a positive correlation between Fn14 and CXCL16 mRNA expression and an inverse correlation between Fn14 and Klotho mRNA. Tubular cells were the site of Fn14, CXCL16 and Klotho expression in vivo. Research on the relationships between these three molecules disclosed that TWEAK activation of Fn14 promoted inflammation through secretion of chemokines such as CXL16 in tubular cells in culture and in vivo. Furthermore, TWEAK activation of Fn14 decreased expression of Klotho mRNA and protein in culture and in vivo. Interestingly, both TWEAK activation of CXCL16 mRNA transcription and suppression of Klotho mRNA transcription were mediated by the NFκB transcription factor. In conclusion, TWEAK engagement of Fn14 is a central event promoting NFκB-mediated activation of inflammation pathways and suppression of anti-inflammatory/anti-ageing pathways. This information may influence future therapeutic approaches to AKI and inflammation/aging.

Saved in:
Bibliographic Details
Main Authors: Izquierdo,M. Concepción, Sanz,Ana B., Sánchez-Niño,M. Dolores, Pérez-Gómez,M. Vanessa, Ruiz-Ortega,Marta, Poveda,Jonay, Ruiz-Andrés,Olga, Ramos,Adrián M., Moreno,Juan A., Egido,Jesús, Ortiz,Alberto
Format: Digital revista
Language:English
Published: Sociedad Española de Nefrología 2012
Online Access:http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0211-69952012000800004
Tags: Add Tag
No Tags, Be the first to tag this record!
id oai:scielo:S0211-69952012000800004
record_format ojs
spelling oai:scielo:S0211-699520120008000042013-01-21Acute kidney injury transcriptomics unveils a relationship between inflammation and ageingIzquierdo,M. ConcepciónSanz,Ana B.Sánchez-Niño,M. DoloresPérez-Gómez,M. VanessaRuiz-Ortega,MartaPoveda,JonayRuiz-Andrés,OlgaRamos,Adrián M.Moreno,Juan A.Egido,JesúsOrtiz,Alberto Acute kidney injury Aging Chronic kidney disease Inflammation Klotho TWEAK There are no pathophysiolgical therapeutic approaches to acute kidney injury (AKI) and the mortality remains high. In addition chronic kidney disease (CKD) predisposes to AKI and AKI contributes to progression of CKD. Recently a transcriptomics approach unveiled a relationship between AKI, inflammation and the regulation of ageing. A transcriptomics analysis of experimental AKI revealed increased kidney expression of Fn14 and transmembrane chemokine CXCL16, as well as a decreased expression of the kidney-secreted anti-ageing hormone Klotho. Fn14 is the receptor for tumor necrosis factor-like weak inducer of apoptosis (TWEAK), a member of the TNF superfamily. In AKI kidneys there was a positive correlation between Fn14 and CXCL16 mRNA expression and an inverse correlation between Fn14 and Klotho mRNA. Tubular cells were the site of Fn14, CXCL16 and Klotho expression in vivo. Research on the relationships between these three molecules disclosed that TWEAK activation of Fn14 promoted inflammation through secretion of chemokines such as CXL16 in tubular cells in culture and in vivo. Furthermore, TWEAK activation of Fn14 decreased expression of Klotho mRNA and protein in culture and in vivo. Interestingly, both TWEAK activation of CXCL16 mRNA transcription and suppression of Klotho mRNA transcription were mediated by the NFκB transcription factor. In conclusion, TWEAK engagement of Fn14 is a central event promoting NFκB-mediated activation of inflammation pathways and suppression of anti-inflammatory/anti-ageing pathways. This information may influence future therapeutic approaches to AKI and inflammation/aging.Sociedad Española de NefrologíaNefrología (Madrid) v.32 n.6 20122012-01-01journal articletext/htmlhttp://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0211-69952012000800004en
institution SCIELO
collection OJS
country España
countrycode ES
component Revista
access En linea
databasecode rev-scielo-es
tag revista
region Europa del Sur
libraryname SciELO
language English
format Digital
author Izquierdo,M. Concepción
Sanz,Ana B.
Sánchez-Niño,M. Dolores
Pérez-Gómez,M. Vanessa
Ruiz-Ortega,Marta
Poveda,Jonay
Ruiz-Andrés,Olga
Ramos,Adrián M.
Moreno,Juan A.
Egido,Jesús
Ortiz,Alberto
spellingShingle Izquierdo,M. Concepción
Sanz,Ana B.
Sánchez-Niño,M. Dolores
Pérez-Gómez,M. Vanessa
Ruiz-Ortega,Marta
Poveda,Jonay
Ruiz-Andrés,Olga
Ramos,Adrián M.
Moreno,Juan A.
Egido,Jesús
Ortiz,Alberto
Acute kidney injury transcriptomics unveils a relationship between inflammation and ageing
author_facet Izquierdo,M. Concepción
Sanz,Ana B.
Sánchez-Niño,M. Dolores
Pérez-Gómez,M. Vanessa
Ruiz-Ortega,Marta
Poveda,Jonay
Ruiz-Andrés,Olga
Ramos,Adrián M.
Moreno,Juan A.
Egido,Jesús
Ortiz,Alberto
author_sort Izquierdo,M. Concepción
title Acute kidney injury transcriptomics unveils a relationship between inflammation and ageing
title_short Acute kidney injury transcriptomics unveils a relationship between inflammation and ageing
title_full Acute kidney injury transcriptomics unveils a relationship between inflammation and ageing
title_fullStr Acute kidney injury transcriptomics unveils a relationship between inflammation and ageing
title_full_unstemmed Acute kidney injury transcriptomics unveils a relationship between inflammation and ageing
title_sort acute kidney injury transcriptomics unveils a relationship between inflammation and ageing
description There are no pathophysiolgical therapeutic approaches to acute kidney injury (AKI) and the mortality remains high. In addition chronic kidney disease (CKD) predisposes to AKI and AKI contributes to progression of CKD. Recently a transcriptomics approach unveiled a relationship between AKI, inflammation and the regulation of ageing. A transcriptomics analysis of experimental AKI revealed increased kidney expression of Fn14 and transmembrane chemokine CXCL16, as well as a decreased expression of the kidney-secreted anti-ageing hormone Klotho. Fn14 is the receptor for tumor necrosis factor-like weak inducer of apoptosis (TWEAK), a member of the TNF superfamily. In AKI kidneys there was a positive correlation between Fn14 and CXCL16 mRNA expression and an inverse correlation between Fn14 and Klotho mRNA. Tubular cells were the site of Fn14, CXCL16 and Klotho expression in vivo. Research on the relationships between these three molecules disclosed that TWEAK activation of Fn14 promoted inflammation through secretion of chemokines such as CXL16 in tubular cells in culture and in vivo. Furthermore, TWEAK activation of Fn14 decreased expression of Klotho mRNA and protein in culture and in vivo. Interestingly, both TWEAK activation of CXCL16 mRNA transcription and suppression of Klotho mRNA transcription were mediated by the NFκB transcription factor. In conclusion, TWEAK engagement of Fn14 is a central event promoting NFκB-mediated activation of inflammation pathways and suppression of anti-inflammatory/anti-ageing pathways. This information may influence future therapeutic approaches to AKI and inflammation/aging.
publisher Sociedad Española de Nefrología
publishDate 2012
url http://scielo.isciii.es/scielo.php?script=sci_arttext&pid=S0211-69952012000800004
work_keys_str_mv AT izquierdomconcepcion acutekidneyinjurytranscriptomicsunveilsarelationshipbetweeninflammationandageing
AT sanzanab acutekidneyinjurytranscriptomicsunveilsarelationshipbetweeninflammationandageing
AT sanchezninomdolores acutekidneyinjurytranscriptomicsunveilsarelationshipbetweeninflammationandageing
AT perezgomezmvanessa acutekidneyinjurytranscriptomicsunveilsarelationshipbetweeninflammationandageing
AT ruizortegamarta acutekidneyinjurytranscriptomicsunveilsarelationshipbetweeninflammationandageing
AT povedajonay acutekidneyinjurytranscriptomicsunveilsarelationshipbetweeninflammationandageing
AT ruizandresolga acutekidneyinjurytranscriptomicsunveilsarelationshipbetweeninflammationandageing
AT ramosadrianm acutekidneyinjurytranscriptomicsunveilsarelationshipbetweeninflammationandageing
AT morenojuana acutekidneyinjurytranscriptomicsunveilsarelationshipbetweeninflammationandageing
AT egidojesus acutekidneyinjurytranscriptomicsunveilsarelationshipbetweeninflammationandageing
AT ortizalberto acutekidneyinjurytranscriptomicsunveilsarelationshipbetweeninflammationandageing
_version_ 1755936350050189312