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Therapeutic Approaches Targeting Proteostasis in Kidney Disease and Fibrosis

Pathological insults usually disturb the folding capacity of cellular proteins and lead to the accumulation of misfolded proteins in the endoplasmic reticulum (ER), which leads to so-called “ER stress”. Increasing evidence indicates that ER stress acts as a trigger factor for the development and pro...

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Autores principales: Chen, Jia-Huang, Wu, Chia-Hsien, Chiang, Chih-Kang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395452/
https://www.ncbi.nlm.nih.gov/pubmed/34445377
http://dx.doi.org/10.3390/ijms22168674
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author Chen, Jia-Huang
Wu, Chia-Hsien
Chiang, Chih-Kang
author_facet Chen, Jia-Huang
Wu, Chia-Hsien
Chiang, Chih-Kang
author_sort Chen, Jia-Huang
collection PubMed
description Pathological insults usually disturb the folding capacity of cellular proteins and lead to the accumulation of misfolded proteins in the endoplasmic reticulum (ER), which leads to so-called “ER stress”. Increasing evidence indicates that ER stress acts as a trigger factor for the development and progression of many kidney diseases. The unfolded protein responses (UPRs), a set of molecular signals that resume proteostasis under ER stress, are thought to restore the adaptive process in chronic kidney disease (CKD) and renal fibrosis. Furthermore, the idea of targeting UPRs for CKD treatment has been well discussed in the past decade. This review summarizes the up-to-date literature regarding studies on the relationship between the UPRs, systemic fibrosis, and renal diseases. We also address the potential therapeutic possibilities of renal diseases based on the modulation of UPRs and ER proteostasis. Finally, we list some of the current UPR modulators and their therapeutic potentials.
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spelling pubmed-83954522021-08-28 Therapeutic Approaches Targeting Proteostasis in Kidney Disease and Fibrosis Chen, Jia-Huang Wu, Chia-Hsien Chiang, Chih-Kang Int J Mol Sci Review Pathological insults usually disturb the folding capacity of cellular proteins and lead to the accumulation of misfolded proteins in the endoplasmic reticulum (ER), which leads to so-called “ER stress”. Increasing evidence indicates that ER stress acts as a trigger factor for the development and progression of many kidney diseases. The unfolded protein responses (UPRs), a set of molecular signals that resume proteostasis under ER stress, are thought to restore the adaptive process in chronic kidney disease (CKD) and renal fibrosis. Furthermore, the idea of targeting UPRs for CKD treatment has been well discussed in the past decade. This review summarizes the up-to-date literature regarding studies on the relationship between the UPRs, systemic fibrosis, and renal diseases. We also address the potential therapeutic possibilities of renal diseases based on the modulation of UPRs and ER proteostasis. Finally, we list some of the current UPR modulators and their therapeutic potentials. MDPI 2021-08-12 /pmc/articles/PMC8395452/ /pubmed/34445377 http://dx.doi.org/10.3390/ijms22168674 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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/).
spellingShingle Review
Chen, Jia-Huang
Wu, Chia-Hsien
Chiang, Chih-Kang
Therapeutic Approaches Targeting Proteostasis in Kidney Disease and Fibrosis
title Therapeutic Approaches Targeting Proteostasis in Kidney Disease and Fibrosis
title_full Therapeutic Approaches Targeting Proteostasis in Kidney Disease and Fibrosis
title_fullStr Therapeutic Approaches Targeting Proteostasis in Kidney Disease and Fibrosis
title_full_unstemmed Therapeutic Approaches Targeting Proteostasis in Kidney Disease and Fibrosis
title_short Therapeutic Approaches Targeting Proteostasis in Kidney Disease and Fibrosis
title_sort therapeutic approaches targeting proteostasis in kidney disease and fibrosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8395452/
https://www.ncbi.nlm.nih.gov/pubmed/34445377
http://dx.doi.org/10.3390/ijms22168674
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