Live Cell Imaging of ATP Levels Reveals Metabolic Compartmentalization within Motoneurons and Early Metabolic Changes in FUS ALS Motoneurons

• Published in: Cells (Basel, Switzerland) Vol. 12; no. 10; p. 1352
• Main Authors: Zimyanin, Vitaly L, Pielka, Anna-Maria, Glaß, Hannes, Japtok, Julia, Großmann, Dajana, Martin, Melanie, Deussen, Andreas, Szewczyk, Barbara, Deppmann, Chris, Zunder, Eli, Andersen, Peter M, Boeckers, Tobias M, Sterneckert, Jared, Redemann, Stefanie, Storch, Alexander, Hermann, Andreas
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 09-05-2023; MDPI
• Subjects: Adenosine Triphosphate - metabolism; Amyotrophic lateral sclerosis; Amyotrophic Lateral Sclerosis - metabolism; Cell differentiation; Cytoplasm; Fibroblasts; FUS gene; FUS protein; Homeostasis; Humans; Localization; Metabolic rate; Metabolism; Mitochondria; Mitochondria - metabolism; Motor neurons; Motor Neurons - metabolism; Mutation; Neurodegenerative diseases; Neurons; Phenotypes; Proteins; RNA-Binding Protein FUS - genetics; RNA-Binding Protein FUS - metabolism; RNA-Binding Protein FUS - pharmacology; Sarcoma; Stem cells; Ultrastructure; United States > US; amyotrophic lateral sclerosis; mitochondria; metabolism
• ISSN: 2073-4409; 2073-4409
• DOI: 10.3390/cells12101352

Motoneurons are one of the most energy-demanding cell types and a primary target in Amyotrophic lateral sclerosis (ALS), a debilitating and lethal neurodegenerative disorder without currently available effective treatments. Disruption of mitochondrial ultrastructure, transport, and metabolism is a commonly reported phenotype in ALS models and can critically affect survival and the proper function of motor neurons. However, how changes in metabolic rates contribute to ALS progression is not fully understood yet. Here, we utilize hiPCS-derived motoneuron cultures and live imaging quantitative techniques to evaluate metabolic rates in fused in sarcoma (FUS)-ALS model cells. We show that differentiation and maturation of motoneurons are accompanied by an overall upregulation of mitochondrial components and a significant increase in metabolic rates that correspond to their high energy-demanding state. Detailed compartment-specific live measurements using a fluorescent ATP sensor and FLIM imaging show significantly lower levels of ATP in the somas of cells carrying FUS-ALS mutations. These changes lead to the increased vulnerability of diseased motoneurons to further metabolic challenges with mitochondrial inhibitors and could be due to the disruption of mitochondrial inner membrane integrity and an increase in its proton leakage. Furthermore, our measurements demonstrate heterogeneity between axonal and somatic compartments, with lower relative levels of ATP in axons. Our observations strongly support the hypothesis that mutated FUS impacts the metabolic states of motoneurons and makes them more susceptible to further neurodegenerative mechanisms.