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Neuroserpin Inclusion Bodies in a FENIB Yeast Model
FENIB (familial encephalopathy with neuroserpin inclusion bodies) is a human monogenic disease caused by point mutations in the SERPINI1 gene, characterized by the intracellular deposition of polymers of neuroserpin (NS), which leads to proteotoxicity and cell death. Despite the different cell and a...
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/PMC8305157/ https://www.ncbi.nlm.nih.gov/pubmed/34361933 http://dx.doi.org/10.3390/microorganisms9071498 |
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author | Vapore, Valentina Mazzaglia, Corrado Sibilia, Diego Del Vecchio, Mara Fruhmann, Gernot Valenti, Marta Miranda, Elena Rinaldi, Teresa Winderickx, Joris Mazzoni, Cristina |
author_facet | Vapore, Valentina Mazzaglia, Corrado Sibilia, Diego Del Vecchio, Mara Fruhmann, Gernot Valenti, Marta Miranda, Elena Rinaldi, Teresa Winderickx, Joris Mazzoni, Cristina |
author_sort | Vapore, Valentina |
collection | PubMed |
description | FENIB (familial encephalopathy with neuroserpin inclusion bodies) is a human monogenic disease caused by point mutations in the SERPINI1 gene, characterized by the intracellular deposition of polymers of neuroserpin (NS), which leads to proteotoxicity and cell death. Despite the different cell and animal models developed thus far, the exact mechanism of cell toxicity elicited by NS polymers remains unclear. Here, we report that human wild-type NS and the polymerogenic variant G392E NS form protein aggregates mainly localized within the endoplasmic reticulum (ER) when expressed in the yeast S. cerevisiae. The expression of NS in yeast delayed the exit from the lag phase, suggesting that NS inclusions cause cellular stress. The cells also showed a higher resistance following mild oxidative stress treatments when compared to control cells. Furthermore, the expression of NS in a pro-apoptotic mutant strain-induced cell death during aging. Overall, these data recapitulate phenotypes observed in mammalian cells, thereby validating S. cerevisiae as a model for FENIB. |
format | Online Article Text |
id | pubmed-8305157 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83051572021-07-25 Neuroserpin Inclusion Bodies in a FENIB Yeast Model Vapore, Valentina Mazzaglia, Corrado Sibilia, Diego Del Vecchio, Mara Fruhmann, Gernot Valenti, Marta Miranda, Elena Rinaldi, Teresa Winderickx, Joris Mazzoni, Cristina Microorganisms Article FENIB (familial encephalopathy with neuroserpin inclusion bodies) is a human monogenic disease caused by point mutations in the SERPINI1 gene, characterized by the intracellular deposition of polymers of neuroserpin (NS), which leads to proteotoxicity and cell death. Despite the different cell and animal models developed thus far, the exact mechanism of cell toxicity elicited by NS polymers remains unclear. Here, we report that human wild-type NS and the polymerogenic variant G392E NS form protein aggregates mainly localized within the endoplasmic reticulum (ER) when expressed in the yeast S. cerevisiae. The expression of NS in yeast delayed the exit from the lag phase, suggesting that NS inclusions cause cellular stress. The cells also showed a higher resistance following mild oxidative stress treatments when compared to control cells. Furthermore, the expression of NS in a pro-apoptotic mutant strain-induced cell death during aging. Overall, these data recapitulate phenotypes observed in mammalian cells, thereby validating S. cerevisiae as a model for FENIB. MDPI 2021-07-13 /pmc/articles/PMC8305157/ /pubmed/34361933 http://dx.doi.org/10.3390/microorganisms9071498 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 | Article Vapore, Valentina Mazzaglia, Corrado Sibilia, Diego Del Vecchio, Mara Fruhmann, Gernot Valenti, Marta Miranda, Elena Rinaldi, Teresa Winderickx, Joris Mazzoni, Cristina Neuroserpin Inclusion Bodies in a FENIB Yeast Model |
title | Neuroserpin Inclusion Bodies in a FENIB Yeast Model |
title_full | Neuroserpin Inclusion Bodies in a FENIB Yeast Model |
title_fullStr | Neuroserpin Inclusion Bodies in a FENIB Yeast Model |
title_full_unstemmed | Neuroserpin Inclusion Bodies in a FENIB Yeast Model |
title_short | Neuroserpin Inclusion Bodies in a FENIB Yeast Model |
title_sort | neuroserpin inclusion bodies in a fenib yeast model |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8305157/ https://www.ncbi.nlm.nih.gov/pubmed/34361933 http://dx.doi.org/10.3390/microorganisms9071498 |
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