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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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. |
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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. 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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.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>38362803</pmid><doi>10.1111/febs.17083</doi><tpages>25</tpages><orcidid>https://orcid.org/0000-0001-8080-2801</orcidid><orcidid>https://orcid.org/0000-0003-4834-7970</orcidid><orcidid>https://orcid.org/0000-0002-0443-6114</orcidid><orcidid>https://orcid.org/0000-0002-3702-6429</orcidid><orcidid>https://orcid.org/0000-0003-1694-931X</orcidid><orcidid>https://orcid.org/0000-0002-7971-4289</orcidid><oa>free_for_read</oa></addata></record> |
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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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