amelia morrone

associated professor

University of Florence
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Articles (13)

Gaucher disease (GD) is a rare genetic metabolic disorder characterized by a dysfunction of the lysosomal glycoside hydrolase glucocerebrosidase (GCase) due to mutations in the gene GBA1, leading to the cellular accumulation of glucosylceramide (GlcCer). While most of the current research focuses on the primary accumulated material, lesser attention has been paid to secondary storage materials and their reciprocal intertwining. By using a novel approach based on flow cytometry and fluorescent labelling, we monitored changes in storage materials directly in fibroblasts derived from GD patients carrying N370S/RecNcil and homozygous L444P or R131C mutations with respect to wild type. In L444P and R131C fibroblasts, we detected not only the primary accumulation of GlcCer accumulation but also a considerable secondary increase in GM1 storage, comparable with the one observed in infantile patients affected by GM1 gangliosidosis. In addition, the ability of a trivalent trihydroxypiperidine iminosugar compound (CV82), which previously showed good pharmacological chaperone activity on GCase enzyme, to reduce the levels of storage materials in L444P and R131C fibroblasts was tested. Interestingly, treatment with different concentrations of CV82 led to a significant reduction in GM1 accumulation only in L444P fibroblasts, without significantly affecting GlcCer levels. The compound CV82 was selective against the GCase enzyme with respect to the β-Galactosidase enzyme, which was responsible for the catabolism of GM1 ganglioside. The reduction in GM1-ganglioside level cannot be therefore ascribed to a direct action of CV82 on β-Galactosidase enzyme, suggesting that GM1 decrease is rather related to other unknown mechanisms that follow the direct action of CV82 on GCase. In conclusion, this work indicates that the tracking of secondary storages can represent a key step for a better understanding of the pathways involved in the severity of GD, also underlying the importance of developing drugs able to reduce both primary and secondary storage-material accumulations in GD.

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2024

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2024

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2024

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2024

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2023

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2023

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2022

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2022

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2022

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2022

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2022

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2020

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2020

Collaborators (22)

Elena Barbieri

Associated Professor in Applied Biology

Università degli Studi di Udine

ITALY
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Laura Rapisarda

University of Catania

ITALY
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Carlo Dionisi-Vici

Head of the Division

Ospedale Pediatrico Bambino Gesù

ITALY
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Paolo Paoli

Associate Professor

University of Florence

ITALY
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Martina Cacciarini

-

ITALY
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Damiana Pieragostino

University of Chieti-Pescara

ITALY
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Macarena Martínez-Bailén

-

SPAIN
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Claudia Rossi

Assistant Professor in Molecular Biology

University of Chieti-Pescara

ITALY
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Giulia Frisso

University of Naples Federico II

ITALY
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Margherita RUOPPOLO

University of Naples Federico II

ITALY
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FRANCESCA NARDECCHIA

Sapienza University of Rome

ITALY
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Gaetano Bertino

Associate Professor of Gastroenterology

University of Catania

ITALY
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Ines Bucci

University of Chieti-Pescara

ITALY
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Rita Barone

University of Catania

ITALY
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Vilberto Stocchi

Professore

University of Urbino

ITALY
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Francesca Cardona

-

ITALY
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Martino Calamai

University of Florence

ITALY
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Pierandrea Lo Nostro

University of Florence

ITALY
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alessandro salina

Istituto Giannina Gaslini

ITALY
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Camilla Matassini

-

ITALY
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Matteo Lulli

University of Florence

ITALY
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Alberto B. Burlina

-

ITALY
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