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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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Detalles Bibliográficos
Autor principal: Žerovnik, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
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.
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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
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