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.

Goglia, I., Węglarz‐tomczak, E., Gioia, C., Liu, Y., Virtuoso, A., Bonanomi, M., et al. (2024). Fusion–fission–mitophagy cycling and metabolic reprogramming coordinate nerve growth factor (NGF)‐dependent neuronal differentiation. THE FEBS JOURNAL [10.1111/febs.17083].

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

Goglia, Ilaria
Co-primo
;
Gioia, Claudio
Co-primo
;
Virtuoso, Assunta;Bonanomi, Marcella;Gaglio, Daniela;Salmistraro, Noemi;Alberghina, Lilia;Colangelo, Anna Maria
Ultimo
2024

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.
Articolo in rivista - Articolo scientifico
computational modeling; metabolism; mitochondrial dynamics; mitophagy; NGF differentiation;
English
16-feb-2024
2024
open
Goglia, I., Węglarz‐tomczak, E., Gioia, C., Liu, Y., Virtuoso, A., Bonanomi, M., et al. (2024). Fusion–fission–mitophagy cycling and metabolic reprogramming coordinate nerve growth factor (NGF)‐dependent neuronal differentiation. THE FEBS JOURNAL [10.1111/febs.17083].
File in questo prodotto:
File Dimensione Formato  
Goglia-2024- FEBS J-VoR.pdf

accesso aperto

Tipologia di allegato: Publisher’s Version (Version of Record, VoR)
Licenza: Creative Commons
Dimensione 12.43 MB
Formato Adobe PDF
12.43 MB Adobe PDF Visualizza/Apri

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/460858
Citazioni
  • Scopus 0
  • ???jsp.display-item.citation.isi??? 0
Social impact