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.

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. - In: MICROORGANISMS. - ISSN 2076-2607. - 9:7(2021), pp. 1-14. [10.3390/microorganisms9071498]

Neuroserpin Inclusion Bodies in a FENIB Yeast Model

Vapore, Valentina
Primo
Methodology
;
Miranda, Elena
Membro del Collaboration Group
;
Rinaldi, Teresa
Membro del Collaboration Group
;
Mazzoni, Cristina
Ultimo
Conceptualization
2021

Abstract

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.
2021
yeast; neurodegeneration; FENIB; protein aggregation
01 Pubblicazione su rivista::01a Articolo in rivista
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. - In: MICROORGANISMS. - ISSN 2076-2607. - 9:7(2021), pp. 1-14. [10.3390/microorganisms9071498]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1564262
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