Loading…

The Signaling Pathway of TNF Receptors: Linking Animal Models of Renal Disease to Human CKD

Chronic kidney disease (CKD) has been recognized as a global public health problem. Despite the current advances in medicine, CKD-associated morbidity and mortality remain unacceptably high. Several studies have highlighted the contribution of inflammation and inflammatory mediators to the developme...

Full description

Saved in:
Bibliographic Details
Published in:International journal of molecular sciences 2022-03, Vol.23 (6), p.3284
Main Authors: Lousa, Irina, Reis, Flávio, Santos-Silva, Alice, Belo, Luís
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c478t-a03c03376e547ab0d5e5f71d03a4b6be751219a4aabb6f4c7a3c9d9046bdbd133
cites cdi_FETCH-LOGICAL-c478t-a03c03376e547ab0d5e5f71d03a4b6be751219a4aabb6f4c7a3c9d9046bdbd133
container_end_page
container_issue 6
container_start_page 3284
container_title International journal of molecular sciences
container_volume 23
creator Lousa, Irina
Reis, Flávio
Santos-Silva, Alice
Belo, Luís
description Chronic kidney disease (CKD) has been recognized as a global public health problem. Despite the current advances in medicine, CKD-associated morbidity and mortality remain unacceptably high. Several studies have highlighted the contribution of inflammation and inflammatory mediators to the development and/or progression of CKD, such as tumor necrosis factor (TNF)-related biomarkers. The inflammation pathway driven by TNF-α, through TNF receptors 1 (TNFR1) and 2 (TNFR2), involves important mediators in the pathogenesis of CKD. Circulating levels of TNFRs were associated with changes in other biomarkers of kidney function and injury, and were described as predictors of disease progression, cardiovascular morbidity, and mortality in several cohorts of patients. Experimental studies describe the possible downstream signaling pathways induced upon TNFR activation and the resulting biological responses. This review will focus on the available data on TNFR1 and TNFR2, and illustrates their contributions to the pathophysiology of kidney diseases, their cellular and molecular roles, as well as their potential as CKD biomarkers. The emerging evidence shows that TNF receptors could act as biomarkers of renal damage and as mediators of the disease. Furthermore, it has been suggested that these biomarkers could significantly improve the discrimination of clinical CKD prognostic models.
doi_str_mv 10.3390/ijms23063284
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_fcf019fe671a4f5cbdb8f8bb1505c626</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_fcf019fe671a4f5cbdb8f8bb1505c626</doaj_id><sourcerecordid>2642433585</sourcerecordid><originalsourceid>FETCH-LOGICAL-c478t-a03c03376e547ab0d5e5f71d03a4b6be751219a4aabb6f4c7a3c9d9046bdbd133</originalsourceid><addsrcrecordid>eNpdkktvEzEQgFeIipbCjTOyxIUDKX7vLodKVfpUw0MlnDhYY6-dOOyug71b1H-P05Qq5TTWzOdPM_YUxRuCjxir8Ue_6hJlWDJa8WfFAeGUTjCW5fOd837xMqUVxpRRUb8o9pnIdIn5QfFzvrTou1_00Pp-gb7BsPwDdyg4NP9yjm6sseshxPQJzXz_a0Oc9L6DFn0OjW3Thrux-S469clCsmgI6HLsoEfT69NXxZ6DNtnXD_Gw-HF-Np9eTmZfL66mJ7OJ4WU1TAAzgxkrpRW8BI0bYYUrSYMZcC21LQWhpAYOoLV03JTATN3UmEvd6IYwdlhcbb1NgJVax9xgvFMBvLpPhLhQEAdvWquccZjUzsqSAHfCZEPlKq2JwMJIKrPreOtaj7qzjbH9EKF9In1a6f1SLcKtquqsqKsseP8giOH3aNOgOp-MbVvobRiTopJzjFnFN-i7_9BVGGN-zXuKcsZEJTL1YUuZGFKK1j02Q7DabIDa3YCMv90d4BH-9-XsL-flq5w</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2642433585</pqid></control><display><type>article</type><title>The Signaling Pathway of TNF Receptors: Linking Animal Models of Renal Disease to Human CKD</title><source>PubMed</source><source>ProQuest - Publicly Available Content Database</source><creator>Lousa, Irina ; Reis, Flávio ; Santos-Silva, Alice ; Belo, Luís</creator><creatorcontrib>Lousa, Irina ; Reis, Flávio ; Santos-Silva, Alice ; Belo, Luís</creatorcontrib><description>Chronic kidney disease (CKD) has been recognized as a global public health problem. Despite the current advances in medicine, CKD-associated morbidity and mortality remain unacceptably high. Several studies have highlighted the contribution of inflammation and inflammatory mediators to the development and/or progression of CKD, such as tumor necrosis factor (TNF)-related biomarkers. The inflammation pathway driven by TNF-α, through TNF receptors 1 (TNFR1) and 2 (TNFR2), involves important mediators in the pathogenesis of CKD. Circulating levels of TNFRs were associated with changes in other biomarkers of kidney function and injury, and were described as predictors of disease progression, cardiovascular morbidity, and mortality in several cohorts of patients. Experimental studies describe the possible downstream signaling pathways induced upon TNFR activation and the resulting biological responses. This review will focus on the available data on TNFR1 and TNFR2, and illustrates their contributions to the pathophysiology of kidney diseases, their cellular and molecular roles, as well as their potential as CKD biomarkers. The emerging evidence shows that TNF receptors could act as biomarkers of renal damage and as mediators of the disease. Furthermore, it has been suggested that these biomarkers could significantly improve the discrimination of clinical CKD prognostic models.</description><identifier>ISSN: 1422-0067</identifier><identifier>ISSN: 1661-6596</identifier><identifier>EISSN: 1422-0067</identifier><identifier>DOI: 10.3390/ijms23063284</identifier><identifier>PMID: 35328704</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>Animal models ; Animals ; Apoptosis ; Biological effects ; Biomarkers ; Cardiovascular diseases ; Cell growth ; CKD ; Cytokines ; Diabetes ; Extracellular matrix ; Fibroblasts ; Humans ; Inflammation ; Kidney diseases ; Kinases ; Ligands ; Metabolism ; Models, Animal ; Morbidity ; Mortality ; Oxidative stress ; Pathogenesis ; Proteins ; Public health ; Receptors, Tumor Necrosis Factor, Type I - metabolism ; Receptors, Tumor Necrosis Factor, Type II - metabolism ; Renal Insufficiency, Chronic ; Review ; Risk factors ; Signal Transduction ; TNF-alpha ; TNFR ; Tumor necrosis factor receptors ; Tumor Necrosis Factor-alpha ; Tumor necrosis factor-TNF ; Tumor necrosis factor-α</subject><ispartof>International journal of molecular sciences, 2022-03, Vol.23 (6), p.3284</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c478t-a03c03376e547ab0d5e5f71d03a4b6be751219a4aabb6f4c7a3c9d9046bdbd133</citedby><cites>FETCH-LOGICAL-c478t-a03c03376e547ab0d5e5f71d03a4b6be751219a4aabb6f4c7a3c9d9046bdbd133</cites><orcidid>0000-0002-3941-6850 ; 0000-0001-8257-5841 ; 0000-0003-3401-9554</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2642433585/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2642433585?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35328704$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lousa, Irina</creatorcontrib><creatorcontrib>Reis, Flávio</creatorcontrib><creatorcontrib>Santos-Silva, Alice</creatorcontrib><creatorcontrib>Belo, Luís</creatorcontrib><title>The Signaling Pathway of TNF Receptors: Linking Animal Models of Renal Disease to Human CKD</title><title>International journal of molecular sciences</title><addtitle>Int J Mol Sci</addtitle><description>Chronic kidney disease (CKD) has been recognized as a global public health problem. Despite the current advances in medicine, CKD-associated morbidity and mortality remain unacceptably high. Several studies have highlighted the contribution of inflammation and inflammatory mediators to the development and/or progression of CKD, such as tumor necrosis factor (TNF)-related biomarkers. The inflammation pathway driven by TNF-α, through TNF receptors 1 (TNFR1) and 2 (TNFR2), involves important mediators in the pathogenesis of CKD. Circulating levels of TNFRs were associated with changes in other biomarkers of kidney function and injury, and were described as predictors of disease progression, cardiovascular morbidity, and mortality in several cohorts of patients. Experimental studies describe the possible downstream signaling pathways induced upon TNFR activation and the resulting biological responses. This review will focus on the available data on TNFR1 and TNFR2, and illustrates their contributions to the pathophysiology of kidney diseases, their cellular and molecular roles, as well as their potential as CKD biomarkers. The emerging evidence shows that TNF receptors could act as biomarkers of renal damage and as mediators of the disease. Furthermore, it has been suggested that these biomarkers could significantly improve the discrimination of clinical CKD prognostic models.</description><subject>Animal models</subject><subject>Animals</subject><subject>Apoptosis</subject><subject>Biological effects</subject><subject>Biomarkers</subject><subject>Cardiovascular diseases</subject><subject>Cell growth</subject><subject>CKD</subject><subject>Cytokines</subject><subject>Diabetes</subject><subject>Extracellular matrix</subject><subject>Fibroblasts</subject><subject>Humans</subject><subject>Inflammation</subject><subject>Kidney diseases</subject><subject>Kinases</subject><subject>Ligands</subject><subject>Metabolism</subject><subject>Models, Animal</subject><subject>Morbidity</subject><subject>Mortality</subject><subject>Oxidative stress</subject><subject>Pathogenesis</subject><subject>Proteins</subject><subject>Public health</subject><subject>Receptors, Tumor Necrosis Factor, Type I - metabolism</subject><subject>Receptors, Tumor Necrosis Factor, Type II - metabolism</subject><subject>Renal Insufficiency, Chronic</subject><subject>Review</subject><subject>Risk factors</subject><subject>Signal Transduction</subject><subject>TNF-alpha</subject><subject>TNFR</subject><subject>Tumor necrosis factor receptors</subject><subject>Tumor Necrosis Factor-alpha</subject><subject>Tumor necrosis factor-TNF</subject><subject>Tumor necrosis factor-α</subject><issn>1422-0067</issn><issn>1661-6596</issn><issn>1422-0067</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkktvEzEQgFeIipbCjTOyxIUDKX7vLodKVfpUw0MlnDhYY6-dOOyug71b1H-P05Qq5TTWzOdPM_YUxRuCjxir8Ue_6hJlWDJa8WfFAeGUTjCW5fOd837xMqUVxpRRUb8o9pnIdIn5QfFzvrTou1_00Pp-gb7BsPwDdyg4NP9yjm6sseshxPQJzXz_a0Oc9L6DFn0OjW3Thrux-S469clCsmgI6HLsoEfT69NXxZ6DNtnXD_Gw-HF-Np9eTmZfL66mJ7OJ4WU1TAAzgxkrpRW8BI0bYYUrSYMZcC21LQWhpAYOoLV03JTATN3UmEvd6IYwdlhcbb1NgJVax9xgvFMBvLpPhLhQEAdvWquccZjUzsqSAHfCZEPlKq2JwMJIKrPreOtaj7qzjbH9EKF9In1a6f1SLcKtquqsqKsseP8giOH3aNOgOp-MbVvobRiTopJzjFnFN-i7_9BVGGN-zXuKcsZEJTL1YUuZGFKK1j02Q7DabIDa3YCMv90d4BH-9-XsL-flq5w</recordid><startdate>20220318</startdate><enddate>20220318</enddate><creator>Lousa, Irina</creator><creator>Reis, Flávio</creator><creator>Santos-Silva, Alice</creator><creator>Belo, Luís</creator><general>MDPI AG</general><general>MDPI</general><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>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0002-3941-6850</orcidid><orcidid>https://orcid.org/0000-0001-8257-5841</orcidid><orcidid>https://orcid.org/0000-0003-3401-9554</orcidid></search><sort><creationdate>20220318</creationdate><title>The Signaling Pathway of TNF Receptors: Linking Animal Models of Renal Disease to Human CKD</title><author>Lousa, Irina ; Reis, Flávio ; Santos-Silva, Alice ; Belo, Luís</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c478t-a03c03376e547ab0d5e5f71d03a4b6be751219a4aabb6f4c7a3c9d9046bdbd133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Animal models</topic><topic>Animals</topic><topic>Apoptosis</topic><topic>Biological effects</topic><topic>Biomarkers</topic><topic>Cardiovascular diseases</topic><topic>Cell growth</topic><topic>CKD</topic><topic>Cytokines</topic><topic>Diabetes</topic><topic>Extracellular matrix</topic><topic>Fibroblasts</topic><topic>Humans</topic><topic>Inflammation</topic><topic>Kidney diseases</topic><topic>Kinases</topic><topic>Ligands</topic><topic>Metabolism</topic><topic>Models, Animal</topic><topic>Morbidity</topic><topic>Mortality</topic><topic>Oxidative stress</topic><topic>Pathogenesis</topic><topic>Proteins</topic><topic>Public health</topic><topic>Receptors, Tumor Necrosis Factor, Type I - metabolism</topic><topic>Receptors, Tumor Necrosis Factor, Type II - metabolism</topic><topic>Renal Insufficiency, Chronic</topic><topic>Review</topic><topic>Risk factors</topic><topic>Signal Transduction</topic><topic>TNF-alpha</topic><topic>TNFR</topic><topic>Tumor necrosis factor receptors</topic><topic>Tumor Necrosis Factor-alpha</topic><topic>Tumor necrosis factor-TNF</topic><topic>Tumor necrosis factor-α</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lousa, Irina</creatorcontrib><creatorcontrib>Reis, Flávio</creatorcontrib><creatorcontrib>Santos-Silva, Alice</creatorcontrib><creatorcontrib>Belo, Luís</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health &amp; Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest - Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>International journal of molecular sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lousa, Irina</au><au>Reis, Flávio</au><au>Santos-Silva, Alice</au><au>Belo, Luís</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Signaling Pathway of TNF Receptors: Linking Animal Models of Renal Disease to Human CKD</atitle><jtitle>International journal of molecular sciences</jtitle><addtitle>Int J Mol Sci</addtitle><date>2022-03-18</date><risdate>2022</risdate><volume>23</volume><issue>6</issue><spage>3284</spage><pages>3284-</pages><issn>1422-0067</issn><issn>1661-6596</issn><eissn>1422-0067</eissn><abstract>Chronic kidney disease (CKD) has been recognized as a global public health problem. Despite the current advances in medicine, CKD-associated morbidity and mortality remain unacceptably high. Several studies have highlighted the contribution of inflammation and inflammatory mediators to the development and/or progression of CKD, such as tumor necrosis factor (TNF)-related biomarkers. The inflammation pathway driven by TNF-α, through TNF receptors 1 (TNFR1) and 2 (TNFR2), involves important mediators in the pathogenesis of CKD. Circulating levels of TNFRs were associated with changes in other biomarkers of kidney function and injury, and were described as predictors of disease progression, cardiovascular morbidity, and mortality in several cohorts of patients. Experimental studies describe the possible downstream signaling pathways induced upon TNFR activation and the resulting biological responses. This review will focus on the available data on TNFR1 and TNFR2, and illustrates their contributions to the pathophysiology of kidney diseases, their cellular and molecular roles, as well as their potential as CKD biomarkers. The emerging evidence shows that TNF receptors could act as biomarkers of renal damage and as mediators of the disease. Furthermore, it has been suggested that these biomarkers could significantly improve the discrimination of clinical CKD prognostic models.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>35328704</pmid><doi>10.3390/ijms23063284</doi><orcidid>https://orcid.org/0000-0002-3941-6850</orcidid><orcidid>https://orcid.org/0000-0001-8257-5841</orcidid><orcidid>https://orcid.org/0000-0003-3401-9554</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1422-0067
ispartof International journal of molecular sciences, 2022-03, Vol.23 (6), p.3284
issn 1422-0067
1661-6596
1422-0067
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_fcf019fe671a4f5cbdb8f8bb1505c626
source PubMed; ProQuest - Publicly Available Content Database
subjects Animal models
Animals
Apoptosis
Biological effects
Biomarkers
Cardiovascular diseases
Cell growth
CKD
Cytokines
Diabetes
Extracellular matrix
Fibroblasts
Humans
Inflammation
Kidney diseases
Kinases
Ligands
Metabolism
Models, Animal
Morbidity
Mortality
Oxidative stress
Pathogenesis
Proteins
Public health
Receptors, Tumor Necrosis Factor, Type I - metabolism
Receptors, Tumor Necrosis Factor, Type II - metabolism
Renal Insufficiency, Chronic
Review
Risk factors
Signal Transduction
TNF-alpha
TNFR
Tumor necrosis factor receptors
Tumor Necrosis Factor-alpha
Tumor necrosis factor-TNF
Tumor necrosis factor-α
title The Signaling Pathway of TNF Receptors: Linking Animal Models of Renal Disease to Human CKD
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T07%3A10%3A19IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Signaling%20Pathway%20of%20TNF%20Receptors:%20Linking%20Animal%20Models%20of%20Renal%20Disease%20to%20Human%20CKD&rft.jtitle=International%20journal%20of%20molecular%20sciences&rft.au=Lousa,%20Irina&rft.date=2022-03-18&rft.volume=23&rft.issue=6&rft.spage=3284&rft.pages=3284-&rft.issn=1422-0067&rft.eissn=1422-0067&rft_id=info:doi/10.3390/ijms23063284&rft_dat=%3Cproquest_doaj_%3E2642433585%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c478t-a03c03376e547ab0d5e5f71d03a4b6be751219a4aabb6f4c7a3c9d9046bdbd133%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2642433585&rft_id=info:pmid/35328704&rfr_iscdi=true