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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...

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Autores principales: Vapore, Valentina, Mazzaglia, Corrado, Sibilia, Diego, Del Vecchio, Mara, Fruhmann, Gernot, Valenti, Marta, Miranda, Elena, Rinaldi, Teresa, Winderickx, Joris, Mazzoni, Cristina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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