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Strain-Dependent Morphology of Reactive Astrocytes in Human- and Animal-Vole-Adapted Prions

Reactive astrogliosis is one of the pathological hallmarks of prion diseases. Recent studies highlighted the influence of several factors on the astrocyte phenotype in prion diseases, including the brain region involved, the genotype backgrounds of the host, and the prion strain. Elucidating the inf...

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Autores principales: Bruno, Rosalia, Riccardi, Geraldina, Iacobone, Floriana, Chiarotti, Flavia, Pirisinu, Laura, Vanni, Ilaria, Marcon, Stefano, D’Agostino, Claudia, Giovannelli, Matteo, Parchi, Piero, Agrimi, Umberto, Nonno, Romolo, Di Bari, Michele Angelo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216604/
https://www.ncbi.nlm.nih.gov/pubmed/37238627
http://dx.doi.org/10.3390/biom13050757
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author Bruno, Rosalia
Riccardi, Geraldina
Iacobone, Floriana
Chiarotti, Flavia
Pirisinu, Laura
Vanni, Ilaria
Marcon, Stefano
D’Agostino, Claudia
Giovannelli, Matteo
Parchi, Piero
Agrimi, Umberto
Nonno, Romolo
Di Bari, Michele Angelo
author_facet Bruno, Rosalia
Riccardi, Geraldina
Iacobone, Floriana
Chiarotti, Flavia
Pirisinu, Laura
Vanni, Ilaria
Marcon, Stefano
D’Agostino, Claudia
Giovannelli, Matteo
Parchi, Piero
Agrimi, Umberto
Nonno, Romolo
Di Bari, Michele Angelo
author_sort Bruno, Rosalia
collection PubMed
description Reactive astrogliosis is one of the pathological hallmarks of prion diseases. Recent studies highlighted the influence of several factors on the astrocyte phenotype in prion diseases, including the brain region involved, the genotype backgrounds of the host, and the prion strain. Elucidating the influence of prion strains on the astrocyte phenotype may provide crucial insights for developing therapeutic strategies. Here, we investigated the relationship between prion strains and astrocyte phenotype in six human- and animal-vole-adapted strains characterized by distinctive neuropathological features. In particular, we compared astrocyte morphology and astrocyte-associated PrP(Sc) deposition among strains in the same brain region, the mediodorsal thalamic nucleus (MDTN). Astrogliosis was detected to some extent in the MDTN of all analyzed voles. However, we observed variability in the morphological appearance of astrocytes depending on the strain. Astrocytes displayed variability in thickness and length of cellular processes and cellular body size, suggesting strain-specific phenotypes of reactive astrocytes. Remarkably, four out of six strains displayed astrocyte-associated PrP(Sc) deposition, which correlated with the size of astrocytes. Overall, these data show that the heterogeneous reactivity of astrocytes in prion diseases depends at least in part on the infecting prion strains and their specific interaction with astrocytes.
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spelling pubmed-102166042023-05-27 Strain-Dependent Morphology of Reactive Astrocytes in Human- and Animal-Vole-Adapted Prions Bruno, Rosalia Riccardi, Geraldina Iacobone, Floriana Chiarotti, Flavia Pirisinu, Laura Vanni, Ilaria Marcon, Stefano D’Agostino, Claudia Giovannelli, Matteo Parchi, Piero Agrimi, Umberto Nonno, Romolo Di Bari, Michele Angelo Biomolecules Article Reactive astrogliosis is one of the pathological hallmarks of prion diseases. Recent studies highlighted the influence of several factors on the astrocyte phenotype in prion diseases, including the brain region involved, the genotype backgrounds of the host, and the prion strain. Elucidating the influence of prion strains on the astrocyte phenotype may provide crucial insights for developing therapeutic strategies. Here, we investigated the relationship between prion strains and astrocyte phenotype in six human- and animal-vole-adapted strains characterized by distinctive neuropathological features. In particular, we compared astrocyte morphology and astrocyte-associated PrP(Sc) deposition among strains in the same brain region, the mediodorsal thalamic nucleus (MDTN). Astrogliosis was detected to some extent in the MDTN of all analyzed voles. However, we observed variability in the morphological appearance of astrocytes depending on the strain. Astrocytes displayed variability in thickness and length of cellular processes and cellular body size, suggesting strain-specific phenotypes of reactive astrocytes. Remarkably, four out of six strains displayed astrocyte-associated PrP(Sc) deposition, which correlated with the size of astrocytes. Overall, these data show that the heterogeneous reactivity of astrocytes in prion diseases depends at least in part on the infecting prion strains and their specific interaction with astrocytes. MDPI 2023-04-27 /pmc/articles/PMC10216604/ /pubmed/37238627 http://dx.doi.org/10.3390/biom13050757 Text en © 2023 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
Bruno, Rosalia
Riccardi, Geraldina
Iacobone, Floriana
Chiarotti, Flavia
Pirisinu, Laura
Vanni, Ilaria
Marcon, Stefano
D’Agostino, Claudia
Giovannelli, Matteo
Parchi, Piero
Agrimi, Umberto
Nonno, Romolo
Di Bari, Michele Angelo
Strain-Dependent Morphology of Reactive Astrocytes in Human- and Animal-Vole-Adapted Prions
title Strain-Dependent Morphology of Reactive Astrocytes in Human- and Animal-Vole-Adapted Prions
title_full Strain-Dependent Morphology of Reactive Astrocytes in Human- and Animal-Vole-Adapted Prions
title_fullStr Strain-Dependent Morphology of Reactive Astrocytes in Human- and Animal-Vole-Adapted Prions
title_full_unstemmed Strain-Dependent Morphology of Reactive Astrocytes in Human- and Animal-Vole-Adapted Prions
title_short Strain-Dependent Morphology of Reactive Astrocytes in Human- and Animal-Vole-Adapted Prions
title_sort strain-dependent morphology of reactive astrocytes in human- and animal-vole-adapted prions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216604/
https://www.ncbi.nlm.nih.gov/pubmed/37238627
http://dx.doi.org/10.3390/biom13050757
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