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FEBS J ; 291(13): 2811-2835, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38362803

ABSTRACT

Neuronal differentiation is regulated by nerve growth factor (NGF) and other neurotrophins. We explored the impact of NGF on mitochondrial dynamics and metabolism through time-lapse imaging, metabolomics profiling, and computer modeling studies. We show that NGF may direct differentiation by stimulating fission, thereby causing selective mitochondrial network fragmentation and mitophagy, ultimately leading to increased mitochondrial quality and respiration. Then, we reconstructed the dynamic fusion-fission-mitophagy cycling of mitochondria in a computer model, integrating these processes into a single network mechanism. Both the computational model and the simulations are able to reproduce the proposed mechanism in terms of mitochondrial dynamics, levels of reactive oxygen species (ROS), mitophagy, and mitochondrial quality, thus providing a computational tool for the interpretation of the experimental data and for future studies aiming to detail further the action of NGF on mitochondrial processes. We also show that changes in these mitochondrial processes are intertwined with a metabolic function of NGF in differentiation: NGF directs a profound metabolic rearrangement involving glycolysis, TCA cycle, and the pentose phosphate pathway, altering the redox balance. This metabolic rewiring may ensure: (a) supply of both energy and building blocks for the anabolic processes needed for morphological reorganization, as well as (b) redox homeostasis.


Subject(s)
Cell Differentiation , Mitochondria , Mitochondrial Dynamics , Mitophagy , Nerve Growth Factor , Neurons , Reactive Oxygen Species , Nerve Growth Factor/metabolism , Nerve Growth Factor/pharmacology , Nerve Growth Factor/genetics , Mitochondrial Dynamics/drug effects , Animals , Neurons/metabolism , Neurons/cytology , Neurons/drug effects , Mitochondria/metabolism , Reactive Oxygen Species/metabolism , PC12 Cells , Rats , Mitophagy/drug effects , Citric Acid Cycle/drug effects , Glycolysis , Computer Simulation , Metabolic Reprogramming
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