Fusion-fission-mitophagy cycling and metabolic reprogramming coordinate nerve growth factor (NGF)-dependent neuronal differentiation

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 stimula...

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Veröffentlicht in:The FEBS journal 2024-07, Vol.291 (13), p.2811-2835
Hauptverfasser: Goglia, Ilaria, Węglarz-Tomczak, Ewelina, Gioia, Claudio, Liu, Yanhua, Virtuoso, Assunta, Bonanomi, Marcella, Gaglio, Daniela, Salmistraro, Noemi, De Luca, Ciro, Papa, Michele, Alberghina, Lilia, Westerhoff, Hans V, Colangelo, Anna Maria
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container_end_page 2835
container_issue 13
container_start_page 2811
container_title The FEBS journal
container_volume 291
creator Goglia, Ilaria
Węglarz-Tomczak, Ewelina
Gioia, Claudio
Liu, Yanhua
Virtuoso, Assunta
Bonanomi, Marcella
Gaglio, Daniela
Salmistraro, Noemi
De Luca, Ciro
Papa, Michele
Alberghina, Lilia
Westerhoff, Hans V
Colangelo, Anna Maria
description 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.
doi_str_mv 10.1111/febs.17083
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subjects Computational neuroscience
Cycles
Differentiation
Fission
Glycolysis
Growth factors
Homeostasis
Metabolism
Metabolomics
Mitochondria
Mitophagy
Nerve growth factor
Nerves
Neurotrophic factors
Pentose
Pentose phosphate pathway
Reactive oxygen species
Software
Tricarboxylic acid cycle
title Fusion-fission-mitophagy cycling and metabolic reprogramming coordinate nerve growth factor (NGF)-dependent neuronal differentiation
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