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Aberrant Stress Granule Dynamics and Aggrephagy in ALS Pathogenesis
Stress granules are conserved cytosolic ribonucleoprotein (RNP) compartments that undergo dynamic assembly and disassembly by phase separation in response to stressful conditions. Gene mutations may lead to aberrant phase separation of stress granules eliciting irreversible protein aggregations. A s...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468025/ https://www.ncbi.nlm.nih.gov/pubmed/34571896 http://dx.doi.org/10.3390/cells10092247 |
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author | Zhang, Yi Gu, Jiayu Sun, Qiming |
author_facet | Zhang, Yi Gu, Jiayu Sun, Qiming |
author_sort | Zhang, Yi |
collection | PubMed |
description | Stress granules are conserved cytosolic ribonucleoprotein (RNP) compartments that undergo dynamic assembly and disassembly by phase separation in response to stressful conditions. Gene mutations may lead to aberrant phase separation of stress granules eliciting irreversible protein aggregations. A selective autophagy pathway called aggrephagy may partially alleviate the cytotoxicity mediated by these protein aggregates. Cells must perceive when and where the stress granules are transformed into toxic protein aggregates to initiate autophagosomal engulfment for subsequent autolysosomal degradation, therefore, maintaining cellular homeostasis. Indeed, defective aggrephagy has been causally linked to various neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). In this review, we discuss stress granules at the intersection of autophagy and ALS pathogenesis. |
format | Online Article Text |
id | pubmed-8468025 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-84680252021-09-27 Aberrant Stress Granule Dynamics and Aggrephagy in ALS Pathogenesis Zhang, Yi Gu, Jiayu Sun, Qiming Cells Review Stress granules are conserved cytosolic ribonucleoprotein (RNP) compartments that undergo dynamic assembly and disassembly by phase separation in response to stressful conditions. Gene mutations may lead to aberrant phase separation of stress granules eliciting irreversible protein aggregations. A selective autophagy pathway called aggrephagy may partially alleviate the cytotoxicity mediated by these protein aggregates. Cells must perceive when and where the stress granules are transformed into toxic protein aggregates to initiate autophagosomal engulfment for subsequent autolysosomal degradation, therefore, maintaining cellular homeostasis. Indeed, defective aggrephagy has been causally linked to various neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). In this review, we discuss stress granules at the intersection of autophagy and ALS pathogenesis. MDPI 2021-08-30 /pmc/articles/PMC8468025/ /pubmed/34571896 http://dx.doi.org/10.3390/cells10092247 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 Zhang, Yi Gu, Jiayu Sun, Qiming Aberrant Stress Granule Dynamics and Aggrephagy in ALS Pathogenesis |
title | Aberrant Stress Granule Dynamics and Aggrephagy in ALS Pathogenesis |
title_full | Aberrant Stress Granule Dynamics and Aggrephagy in ALS Pathogenesis |
title_fullStr | Aberrant Stress Granule Dynamics and Aggrephagy in ALS Pathogenesis |
title_full_unstemmed | Aberrant Stress Granule Dynamics and Aggrephagy in ALS Pathogenesis |
title_short | Aberrant Stress Granule Dynamics and Aggrephagy in ALS Pathogenesis |
title_sort | aberrant stress granule dynamics and aggrephagy in als pathogenesis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8468025/ https://www.ncbi.nlm.nih.gov/pubmed/34571896 http://dx.doi.org/10.3390/cells10092247 |
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