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Glial-derived mitochondrial signals impact neuronal proteostasis and aging
The nervous system plays a critical role in maintaining whole-organism homeostasis; neurons experiencing mitochondrial stress can coordinate the induction of protective cellular pathways, such as the mitochondrial unfolded protein response (UPR(MT)), between tissues. However, these studies largely i...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441375/ https://www.ncbi.nlm.nih.gov/pubmed/37609253 http://dx.doi.org/10.1101/2023.07.20.549924 |
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author | Bar-Ziv, Raz Dutta, Naibedya Hruby, Adam Sukarto, Edward Averbukh, Maxim Alcala, Athena Henderson, Hope R. Durieux, Jenni Tronnes, Sarah U. Ahmad, Qazi Bolas, Theodore Perez, Joel Dishart, Julian G. Vega, Matthew Garcia, Gilberto Higuchi-Sanabria, Ryo Dillin, Andrew |
author_facet | Bar-Ziv, Raz Dutta, Naibedya Hruby, Adam Sukarto, Edward Averbukh, Maxim Alcala, Athena Henderson, Hope R. Durieux, Jenni Tronnes, Sarah U. Ahmad, Qazi Bolas, Theodore Perez, Joel Dishart, Julian G. Vega, Matthew Garcia, Gilberto Higuchi-Sanabria, Ryo Dillin, Andrew |
author_sort | Bar-Ziv, Raz |
collection | PubMed |
description | The nervous system plays a critical role in maintaining whole-organism homeostasis; neurons experiencing mitochondrial stress can coordinate the induction of protective cellular pathways, such as the mitochondrial unfolded protein response (UPR(MT)), between tissues. However, these studies largely ignored non-neuronal cells of the nervous system. Here, we found that UPR(MT) activation in four, astrocyte-like glial cells in the nematode, C. elegans, can promote protein homeostasis by alleviating protein aggregation in neurons. Surprisingly, we find that glial cells utilize small clear vesicles (SCVs) to signal to neurons, which then relay the signal to the periphery using dense-core vesicles (DCVs). This work underlines the importance of glia in establishing and regulating protein homeostasis within the nervous system, which can then impact neuron-mediated effects in organismal homeostasis and longevity. |
format | Online Article Text |
id | pubmed-10441375 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-104413752023-08-22 Glial-derived mitochondrial signals impact neuronal proteostasis and aging Bar-Ziv, Raz Dutta, Naibedya Hruby, Adam Sukarto, Edward Averbukh, Maxim Alcala, Athena Henderson, Hope R. Durieux, Jenni Tronnes, Sarah U. Ahmad, Qazi Bolas, Theodore Perez, Joel Dishart, Julian G. Vega, Matthew Garcia, Gilberto Higuchi-Sanabria, Ryo Dillin, Andrew bioRxiv Article The nervous system plays a critical role in maintaining whole-organism homeostasis; neurons experiencing mitochondrial stress can coordinate the induction of protective cellular pathways, such as the mitochondrial unfolded protein response (UPR(MT)), between tissues. However, these studies largely ignored non-neuronal cells of the nervous system. Here, we found that UPR(MT) activation in four, astrocyte-like glial cells in the nematode, C. elegans, can promote protein homeostasis by alleviating protein aggregation in neurons. Surprisingly, we find that glial cells utilize small clear vesicles (SCVs) to signal to neurons, which then relay the signal to the periphery using dense-core vesicles (DCVs). This work underlines the importance of glia in establishing and regulating protein homeostasis within the nervous system, which can then impact neuron-mediated effects in organismal homeostasis and longevity. Cold Spring Harbor Laboratory 2023-08-08 /pmc/articles/PMC10441375/ /pubmed/37609253 http://dx.doi.org/10.1101/2023.07.20.549924 Text en https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License (https://creativecommons.org/licenses/by-nc/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Bar-Ziv, Raz Dutta, Naibedya Hruby, Adam Sukarto, Edward Averbukh, Maxim Alcala, Athena Henderson, Hope R. Durieux, Jenni Tronnes, Sarah U. Ahmad, Qazi Bolas, Theodore Perez, Joel Dishart, Julian G. Vega, Matthew Garcia, Gilberto Higuchi-Sanabria, Ryo Dillin, Andrew Glial-derived mitochondrial signals impact neuronal proteostasis and aging |
title | Glial-derived mitochondrial signals impact neuronal proteostasis and aging |
title_full | Glial-derived mitochondrial signals impact neuronal proteostasis and aging |
title_fullStr | Glial-derived mitochondrial signals impact neuronal proteostasis and aging |
title_full_unstemmed | Glial-derived mitochondrial signals impact neuronal proteostasis and aging |
title_short | Glial-derived mitochondrial signals impact neuronal proteostasis and aging |
title_sort | glial-derived mitochondrial signals impact neuronal proteostasis and aging |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10441375/ https://www.ncbi.nlm.nih.gov/pubmed/37609253 http://dx.doi.org/10.1101/2023.07.20.549924 |
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