Cargando…
Autophagy and Renal Fibrosis
Renal fibrosis is a common process of almost all the chronic kidney diseases progressing to end-stage kidney disease. As a highly conserved lysosomal protein degradation pathway, autophagy is responsible for degrading protein aggregates, damaged organelles, or invading pathogens to maintain intracel...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
JKL International LLC
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116923/ https://www.ncbi.nlm.nih.gov/pubmed/35656109 http://dx.doi.org/10.14336/AD.2021.1027 |
_version_ | 1784710215564787712 |
---|---|
author | Liang, Shan Wu, Yun-Shan Li, Dong-Yi Tang, Ji-Xin Liu, Hua-Feng |
author_facet | Liang, Shan Wu, Yun-Shan Li, Dong-Yi Tang, Ji-Xin Liu, Hua-Feng |
author_sort | Liang, Shan |
collection | PubMed |
description | Renal fibrosis is a common process of almost all the chronic kidney diseases progressing to end-stage kidney disease. As a highly conserved lysosomal protein degradation pathway, autophagy is responsible for degrading protein aggregates, damaged organelles, or invading pathogens to maintain intracellular homeostasis. Growing evidence reveals that autophagy is involved in the progression of renal fibrosis, both in the tubulointerstitial compartment and in the glomeruli. Nevertheless, the specific role of autophagy in renal fibrosis has still not been fully understood. Therefore, in this review we will describe the characteristics of autophagy and summarize the recent advances in understanding the functions of autophagy in renal fibrosis. Moreover, the problem existing in this field and the possibility of autophagy as the potential therapeutic target for renal fibrosis have also been discussed. |
format | Online Article Text |
id | pubmed-9116923 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | JKL International LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-91169232022-06-01 Autophagy and Renal Fibrosis Liang, Shan Wu, Yun-Shan Li, Dong-Yi Tang, Ji-Xin Liu, Hua-Feng Aging Dis Review Renal fibrosis is a common process of almost all the chronic kidney diseases progressing to end-stage kidney disease. As a highly conserved lysosomal protein degradation pathway, autophagy is responsible for degrading protein aggregates, damaged organelles, or invading pathogens to maintain intracellular homeostasis. Growing evidence reveals that autophagy is involved in the progression of renal fibrosis, both in the tubulointerstitial compartment and in the glomeruli. Nevertheless, the specific role of autophagy in renal fibrosis has still not been fully understood. Therefore, in this review we will describe the characteristics of autophagy and summarize the recent advances in understanding the functions of autophagy in renal fibrosis. Moreover, the problem existing in this field and the possibility of autophagy as the potential therapeutic target for renal fibrosis have also been discussed. JKL International LLC 2022-06-01 /pmc/articles/PMC9116923/ /pubmed/35656109 http://dx.doi.org/10.14336/AD.2021.1027 Text en Copyright: © 2022 Liang et al. https://creativecommons.org/licenses/by/2.0/this is an open access article distributed under the terms of the creative commons attribution license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Review Liang, Shan Wu, Yun-Shan Li, Dong-Yi Tang, Ji-Xin Liu, Hua-Feng Autophagy and Renal Fibrosis |
title | Autophagy and Renal Fibrosis |
title_full | Autophagy and Renal Fibrosis |
title_fullStr | Autophagy and Renal Fibrosis |
title_full_unstemmed | Autophagy and Renal Fibrosis |
title_short | Autophagy and Renal Fibrosis |
title_sort | autophagy and renal fibrosis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9116923/ https://www.ncbi.nlm.nih.gov/pubmed/35656109 http://dx.doi.org/10.14336/AD.2021.1027 |
work_keys_str_mv | AT liangshan autophagyandrenalfibrosis AT wuyunshan autophagyandrenalfibrosis AT lidongyi autophagyandrenalfibrosis AT tangjixin autophagyandrenalfibrosis AT liuhuafeng autophagyandrenalfibrosis |