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Possible Mechanisms by which Stefin B could Regulate Proteostasis and Oxidative Stress
Human stefin B is a protease inhibitor from the family of cystatins. It was reported that it forms oligomers in cells. We have shown that it has a role in cell’s response to misfolded proteins. We also have shown that its oligomers bind amyloid-beta (Aβ). Here, we discuss ways, how stefin B could re...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2019
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357131/ https://www.ncbi.nlm.nih.gov/pubmed/30669344 http://dx.doi.org/10.3390/cells8010070 |
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author | Žerovnik, Eva |
author_facet | Žerovnik, Eva |
author_sort | Žerovnik, Eva |
collection | PubMed |
description | Human stefin B is a protease inhibitor from the family of cystatins. It was reported that it forms oligomers in cells. We have shown that it has a role in cell’s response to misfolded proteins. We also have shown that its oligomers bind amyloid-beta (Aβ). Here, we discuss ways, how stefin B could reduce build-up of protein aggregates by other proteins and consequently reduces ROS and, how this might be connected to autophagy. When overexpressed, stefin B forms protein aggregates itself and these protein aggregates induce autophagy. Similarly, cystatin C was shown to bind Aβ and to induce autophagy. It is also suggested how more knowledge about the role of stefin B in a cell’s response to misfolded proteins could be used to modulate progressive myoclonus epilepsy of type 1 EPM1 disease. |
format | Online Article Text |
id | pubmed-6357131 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-63571312019-02-06 Possible Mechanisms by which Stefin B could Regulate Proteostasis and Oxidative Stress Žerovnik, Eva Cells Communication Human stefin B is a protease inhibitor from the family of cystatins. It was reported that it forms oligomers in cells. We have shown that it has a role in cell’s response to misfolded proteins. We also have shown that its oligomers bind amyloid-beta (Aβ). Here, we discuss ways, how stefin B could reduce build-up of protein aggregates by other proteins and consequently reduces ROS and, how this might be connected to autophagy. When overexpressed, stefin B forms protein aggregates itself and these protein aggregates induce autophagy. Similarly, cystatin C was shown to bind Aβ and to induce autophagy. It is also suggested how more knowledge about the role of stefin B in a cell’s response to misfolded proteins could be used to modulate progressive myoclonus epilepsy of type 1 EPM1 disease. MDPI 2019-01-18 /pmc/articles/PMC6357131/ /pubmed/30669344 http://dx.doi.org/10.3390/cells8010070 Text en © 2019 by the author. 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Žerovnik, Eva Possible Mechanisms by which Stefin B could Regulate Proteostasis and Oxidative Stress |
title | Possible Mechanisms by which Stefin B could Regulate Proteostasis and Oxidative Stress |
title_full | Possible Mechanisms by which Stefin B could Regulate Proteostasis and Oxidative Stress |
title_fullStr | Possible Mechanisms by which Stefin B could Regulate Proteostasis and Oxidative Stress |
title_full_unstemmed | Possible Mechanisms by which Stefin B could Regulate Proteostasis and Oxidative Stress |
title_short | Possible Mechanisms by which Stefin B could Regulate Proteostasis and Oxidative Stress |
title_sort | possible mechanisms by which stefin b could regulate proteostasis and oxidative stress |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6357131/ https://www.ncbi.nlm.nih.gov/pubmed/30669344 http://dx.doi.org/10.3390/cells8010070 |
work_keys_str_mv | AT zerovnikeva possiblemechanismsbywhichstefinbcouldregulateproteostasisandoxidativestress |