Mitochondrial dysfunction drives a neuronal exhaustion phenotype in methylmalonic aciduria

Methylmalonic aciduria (MMA) is an inborn error of metabolism resulting in loss of function of the enzyme methylmalonyl-CoA mutase (MMUT). Despite acute and persistent neurological symptoms, the pathogenesis of MMA in the central nervous system is poorly understood, which has contributed to a dearth of effective brain specific treatments. Here we utilised patient-derived induced pluripotent stem cells and in vitro differentiation to generate a human neuronal model of MMA. We reveal strong evidence of mitochondrial dysfunction caused by deficiency of MMUT in patient neurons. By employing patch-clamp electrophysiology, targeted metabolomics, and bulk transcriptomics, we expose an altered state of excitability, which is exacerbated by application of dimethyl-2-oxoglutarate, and we suggest may be connected to metabolic rewiring. Our work provides first evidence of mitochondrial driven neuronal dysfunction in MMA, which through our comprehensive characterisation of this paradigmatic model, enables first steps to identifying effective therapies.

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Publication Details

Journal
Communications Biology
Published
2025-03-11
DOI
https://doi.org/10.1038/s42003-025-07828-z
Citations
6
Primary Topic
Metabolism and Genetic Disorders
Type
article
Field-Weighted Citation Impact
7.91

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article

Mitochondrial dysfunction drives a neuronal exhaustion phenotype in methylmalonic aciduria

Federica Conte, Ferdinand von Meyenn, Matthew C.S. Denley, D. Sean Froese et al.
6 citations
Communications Biology
Metabolism and Genetic Disorders
7.91
article

Mitochondrial dysfunction drives a neuronal exhaustion phenotype in methylmalonic aciduria

Federica Conte, Ferdinand von Meyenn, Matthew C.S. Denley, D. Sean Froese, Miriam A. Güra, Straub MS, Matthias R. Baumgartner, Beata Vekeriotaite, Sarah Cherkaoui, David Pentón, Igor Delvendahl, Martin Poms, Giulio Marcionelli
article en
6 citations

Abstract

Methylmalonic aciduria (MMA) is an inborn error of metabolism resulting in loss of function of the enzyme methylmalonyl-CoA mutase (MMUT). Despite acute and persistent neurological symptoms, the pathogenesis of MMA in the central nervous system is poorly understood, which has contributed to a dearth of effective brain specific treatments. Here we utilised patient-derived induced pluripotent stem cells and in vitro differentiation to generate a human neuronal model of MMA. We reveal strong evidence of mitochondrial dysfunction caused by deficiency of MMUT in patient neurons. By employing patch-clamp electrophysiology, targeted metabolomics, and bulk transcriptomics, we expose an altered state of excitability, which is exacerbated by application of dimethyl-2-oxoglutarate, and we suggest may be connected to metabolic rewiring. Our work provides first evidence of mitochondrial driven neuronal dysfunction in MMA, which through our comprehensive characterisation of this paradigmatic model, enables first steps to identifying effective therapies.

Communications BiologyVol. 8(1)
Radboud University Nijmegen (NL), University of Zurich (CH), University Medical Center (US), Radboud University Medical Center (NL), ETH Zurich (CH), University Children's Hospital Zurich (CH)
National Science Foundation, Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung, Universität Zürich
Good health and well-being
Openalex Percentile: Top 3%
Metabolism and Genetic Disorders
7.91
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