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Resident fibroblasts in the kidney: a major driver of fibrosis and inflammation

BACKGROUND: Chronic kidney disease (CKD) is a leading cause of end stage renal disease (ESRD) and cardiovascular morbidity and mortality worldwide, resulting in a growing social and economic burden. The prevalence and burden of CKD is anticipated to further increase over the next decades as a result...

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Autores principales: Sato, Yuki, Yanagita, Motoko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725902/
https://www.ncbi.nlm.nih.gov/pubmed/29259716
http://dx.doi.org/10.1186/s41232-017-0048-3
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author Sato, Yuki
Yanagita, Motoko
author_facet Sato, Yuki
Yanagita, Motoko
author_sort Sato, Yuki
collection PubMed
description BACKGROUND: Chronic kidney disease (CKD) is a leading cause of end stage renal disease (ESRD) and cardiovascular morbidity and mortality worldwide, resulting in a growing social and economic burden. The prevalence and burden of CKD is anticipated to further increase over the next decades as a result of aging. MAIN BODY OF ABSTRACT: In the pathogenesis of CKD, irrespective of the etiology, resident fibroblasts are key players and have been demonstrated to play crucial roles for disease initiation and progression. In response to injury, resident fibroblasts transdifferentiate into myofibroblasts that express alpha smooth muscle actin (αSMA) and have an increased capacity to produce large amounts of extracellular matrix (ECM) proteins, leading to renal fibrosis. In addition to this fundamental role of fibroblasts as drivers for renal fibrosis, growing amounts of evidence have shown that resident fibroblasts are also actively involved in initiating and promoting inflammation during kidney injury. During the myofibroblastic transition described above, resident fibroblasts activate NF-κB signaling and produce pro-inflammatory cytokines and chemokines, promoting inflammation. Furthermore, under aging milieu, resident fibroblasts transdifferentiate into several distinct phenotypic fibroblasts, including CXCL13/CCL19-producing fibroblasts, retinoic acid-producing fibroblasts, and follicular dendritic cells, in response to injury and orchestrate tertiary lymphoid tissue (TLT) formation, which results in uncontrolled aberrant inflammation and retards tissue repair. Anti-inflammatory agents can improve myofibroblastic transdifferentiation and abolish TLT formation, suggesting that targeting these inflammatory fibroblasts can potentially ameliorate kidney disease. SHORT CONCLUSION: Beyond its conventional role as an executor of fibrosis, resident fibroblasts display more pro-inflammatory phenotypes and contribute actively to driving inflammation during kidney injury.
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spelling pubmed-57259022017-12-19 Resident fibroblasts in the kidney: a major driver of fibrosis and inflammation Sato, Yuki Yanagita, Motoko Inflamm Regen Review BACKGROUND: Chronic kidney disease (CKD) is a leading cause of end stage renal disease (ESRD) and cardiovascular morbidity and mortality worldwide, resulting in a growing social and economic burden. The prevalence and burden of CKD is anticipated to further increase over the next decades as a result of aging. MAIN BODY OF ABSTRACT: In the pathogenesis of CKD, irrespective of the etiology, resident fibroblasts are key players and have been demonstrated to play crucial roles for disease initiation and progression. In response to injury, resident fibroblasts transdifferentiate into myofibroblasts that express alpha smooth muscle actin (αSMA) and have an increased capacity to produce large amounts of extracellular matrix (ECM) proteins, leading to renal fibrosis. In addition to this fundamental role of fibroblasts as drivers for renal fibrosis, growing amounts of evidence have shown that resident fibroblasts are also actively involved in initiating and promoting inflammation during kidney injury. During the myofibroblastic transition described above, resident fibroblasts activate NF-κB signaling and produce pro-inflammatory cytokines and chemokines, promoting inflammation. Furthermore, under aging milieu, resident fibroblasts transdifferentiate into several distinct phenotypic fibroblasts, including CXCL13/CCL19-producing fibroblasts, retinoic acid-producing fibroblasts, and follicular dendritic cells, in response to injury and orchestrate tertiary lymphoid tissue (TLT) formation, which results in uncontrolled aberrant inflammation and retards tissue repair. Anti-inflammatory agents can improve myofibroblastic transdifferentiation and abolish TLT formation, suggesting that targeting these inflammatory fibroblasts can potentially ameliorate kidney disease. SHORT CONCLUSION: Beyond its conventional role as an executor of fibrosis, resident fibroblasts display more pro-inflammatory phenotypes and contribute actively to driving inflammation during kidney injury. BioMed Central 2017-08-07 /pmc/articles/PMC5725902/ /pubmed/29259716 http://dx.doi.org/10.1186/s41232-017-0048-3 Text en © The Author(s) 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Sato, Yuki
Yanagita, Motoko
Resident fibroblasts in the kidney: a major driver of fibrosis and inflammation
title Resident fibroblasts in the kidney: a major driver of fibrosis and inflammation
title_full Resident fibroblasts in the kidney: a major driver of fibrosis and inflammation
title_fullStr Resident fibroblasts in the kidney: a major driver of fibrosis and inflammation
title_full_unstemmed Resident fibroblasts in the kidney: a major driver of fibrosis and inflammation
title_short Resident fibroblasts in the kidney: a major driver of fibrosis and inflammation
title_sort resident fibroblasts in the kidney: a major driver of fibrosis and inflammation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5725902/
https://www.ncbi.nlm.nih.gov/pubmed/29259716
http://dx.doi.org/10.1186/s41232-017-0048-3
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