Longitudinal transformation of mitochondrial metabolism during neurogenesis

Neural stem cells (NSCs) are valuable in the quest to conquer neurodegenerative diseases due to their capability to reconstruct the damaged neuronal networks. However, deep understanding of the intercellular signaling mechanism controlling the lineage and fate of the stem cells is required before potential clinical applications. Here, we applied nondestructive and label-free electrochemical methods for the longitudinal tracking of NSC respiratory metabolism. Sharp change in the oxygen utilization pattern was observed concomitant to stemness loss and onset of differentiation, suggesting metabolic reprogramming in the transition. Intra- and extracellular profiling of mitochondrial metabolites revealed molecular preference in the extracellular transport rates. Electrochemical emulation of the metabolite release pattern induced acceleration of neurite growth in nearby cells, suggesting paracrine signaling system mediated by mitochondrial metabolites.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-11-21
DOI
https://doi.org/10.1073/pnas.2517961122
Citations
1
Primary Topic
Neurogenesis and neuroplasticity mechanisms
Type
article
Field-Weighted Citation Impact
1.32
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article

Longitudinal transformation of mitochondrial metabolism during neurogenesis

Geonwoo Park, Yeonsu Kim, Suhyuk Choi, Seung‐Woo Cho et al.
1 citations
Proceedings of the National Academy of Sciences
Neurogenesis and neuroplasticity mechanisms
1.32
article

Longitudinal transformation of mitochondrial metabolism during neurogenesis

Geonwoo Park, Yeonsu Kim, Suhyuk Choi, Seung‐Woo Cho, Woo Yang Pyun, Hyun S. Ahn, Hyun Woo Park, Hyo Jin Gwon, Donghoon Lim, JongWon Kim, Sewon Park, Yunwoo Nam, Jong Seung Lee
article en
1 citations

Abstract

Neural stem cells (NSCs) are valuable in the quest to conquer neurodegenerative diseases due to their capability to reconstruct the damaged neuronal networks. However, deep understanding of the intercellular signaling mechanism controlling the lineage and fate of the stem cells is required before potential clinical applications. Here, we applied nondestructive and label-free electrochemical methods for the longitudinal tracking of NSC respiratory metabolism. Sharp change in the oxygen utilization pattern was observed concomitant to stemness loss and onset of differentiation, suggesting metabolic reprogramming in the transition. Intra- and extracellular profiling of mitochondrial metabolites revealed molecular preference in the extracellular transport rates. Electrochemical emulation of the metabolite release pattern induced acceleration of neurite growth in nearby cells, suggesting paracrine signaling system mediated by mitochondrial metabolites.

Proceedings of the National Academy of SciencesVol. 122(47)
Yonsei University (KR), Institute for Basic Science (KR)
Openalex Percentile: Top 14%
Neurogenesis and neuroplasticity mechanisms
1.32
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Longitudinal transformation of mitochondrial metabolism during neurogenesis — Geonwoo Park, Yeonsu Kim, et al. · Proceedings of the National Academy of Sciences (2025) | TGRS Research Map | TGRS