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Exploring the metabolic signature of Amyotrophic Lateral Sclerosis patients-derived cells

Title: Exploring the metabolic signature of Amyotrophic Lateral Sclerosis patients-derived cells
Authors: Vulcano Edvige; Perciballi Elisa; Ferro Sara; Lombardi Ivan; Carletti Rose Mary; Bovio Federica; Matilde Forcella; Rosati Jessica; Gelati Maurizio; Profico Daniela; Fusi Paola; Vescovi Angelo Luigi; Ferrari Daniela
Contributors: Vulcano, E; Perciballi, E; Ferro, S; Lombardi, I; Carletti Rose Mary; Bovio, F; Forcella, M; Rosati, J; Maurizio, G; Daniela, P; Fusi, P; Vescovi, A; Ferrari, D
Publication Year: 2024
Collection: Università degli Studi di Milano-Bicocca: BOA (Bicocca Open Archive)
Subject Terms: human induced Neural Stem Cells; TDP-43; ALS
Description: Amyotrophic lateral sclerosis (ALS) is a relentlessly fatal neurodegenerative disease characterized by a selective degeneration of upper motor neurons in motor cortex and lower motor neurons in brainstem and spinal cord, leading to rapid paralysis and death1. To date, the pathogenesis is largely unknown and effective therapies still lacking. A massive amount of evidence shows the pivotal role of abnormalities in energy metabolism and mitochondrial dysfunction in ALS, suggesting a strong association between mitochondria metabolism disorder and neurodegeneration2,3. Here, we are elucidating the metabolic profile of patients-derived in vitro models of ALS aiming to obtain a more in-depth understanding of metabolism in health and disease and to provide a platform to unravel the pathological mechanisms underpinning ALS. Defining the role of the impaired metabolism might identify novel therapeutic targets and design innovative treatments for ALS patients.
Document Type: conference object
Language: English
Relation: iPSC Modelling in Neuromuscular Disorders (iMND); https://hdl.handle.net/10281/543109
Availability: https://hdl.handle.net/10281/543109
Accession Number: edsbas.873CD8F1
Database: BASE