Structural Diversity of Mitochondria in the Neuromuscular System across Development Revealed by 3D Electron Microscopy

Abstract As an animal matures, its neural circuit undergoes alterations, yet the developmental changes in intracellular organelles to facilitate these changes is less understood. Using 3D electron microscopy and deep learning, the study develops semi‐automated methods for reconstructing mitochondria...

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Main Authors: J. Alexander Bae, Myung‐kyu Choi, Soungyub Ahn, Gwanho Ko, Daniel T. Choe, Hyunsoo Yim, Ken C. Nguyen, Jinseop S. Kim, David H. Hall, Junho Lee
Format: Article
Language:English
Published: Wiley 2025-05-01
Series:Advanced Science
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Online Access:https://doi.org/10.1002/advs.202411191
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author J. Alexander Bae
Myung‐kyu Choi
Soungyub Ahn
Gwanho Ko
Daniel T. Choe
Hyunsoo Yim
Ken C. Nguyen
Jinseop S. Kim
David H. Hall
Junho Lee
author_facet J. Alexander Bae
Myung‐kyu Choi
Soungyub Ahn
Gwanho Ko
Daniel T. Choe
Hyunsoo Yim
Ken C. Nguyen
Jinseop S. Kim
David H. Hall
Junho Lee
author_sort J. Alexander Bae
collection DOAJ
description Abstract As an animal matures, its neural circuit undergoes alterations, yet the developmental changes in intracellular organelles to facilitate these changes is less understood. Using 3D electron microscopy and deep learning, the study develops semi‐automated methods for reconstructing mitochondria in C. elegans and collected mitochondria reconstructions from normal reproductive stages and dauer, enabling comparative study on mitochondria structure within the neuromuscular system. It is found that various mitochondria structural properties in neurons correlate with synaptic connections and these properties are preserved across development in different neural circuits. To test the necessity of these universal mitochondria properties, the study examines the behavior in drp‐1 mutants with impaired mitochondria fission and discovers that it causes behavioral deficits. Moreover, it is observed that dauer neurons display distinctive mitochondrial features, and mitochondria in dauer muscles exhibit unique reticulum‐like structure. It is proposed that these specialized mitochondria structures may serve as an adaptive mechanism to support stage‐specific behavioral and physiological needs.
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spelling doaj-art-3edcd941041247fca628f0bb8fcc985f2025-08-20T03:20:10ZengWileyAdvanced Science2198-38442025-05-011220n/an/a10.1002/advs.202411191Structural Diversity of Mitochondria in the Neuromuscular System across Development Revealed by 3D Electron MicroscopyJ. Alexander Bae0Myung‐kyu Choi1Soungyub Ahn2Gwanho Ko3Daniel T. Choe4Hyunsoo Yim5Ken C. Nguyen6Jinseop S. Kim7David H. Hall8Junho Lee9Research Institute of Basic Sciences Seoul National University Seoul 08826 Republic of KoreaDepartment of Biological Sciences Seoul National University Seoul 08826 Republic of KoreaDepartment of Biological Sciences Seoul National University Seoul 08826 Republic of KoreaDepartment of Biological Sciences Seoul National University Seoul 08826 Republic of KoreaDepartment of Biological Sciences Seoul National University Seoul 08826 Republic of KoreaDepartment of Biological Sciences Seoul National University Seoul 08826 Republic of KoreaDominick P. Purpura Department of Neuroscience Albert Einstein College of Medicine Bronx NY 10461 USADepartment of Biological Sciences Sungkyunkwan University Suwon 16419 Republic of KoreaDominick P. Purpura Department of Neuroscience Albert Einstein College of Medicine Bronx NY 10461 USAResearch Institute of Basic Sciences Seoul National University Seoul 08826 Republic of KoreaAbstract As an animal matures, its neural circuit undergoes alterations, yet the developmental changes in intracellular organelles to facilitate these changes is less understood. Using 3D electron microscopy and deep learning, the study develops semi‐automated methods for reconstructing mitochondria in C. elegans and collected mitochondria reconstructions from normal reproductive stages and dauer, enabling comparative study on mitochondria structure within the neuromuscular system. It is found that various mitochondria structural properties in neurons correlate with synaptic connections and these properties are preserved across development in different neural circuits. To test the necessity of these universal mitochondria properties, the study examines the behavior in drp‐1 mutants with impaired mitochondria fission and discovers that it causes behavioral deficits. Moreover, it is observed that dauer neurons display distinctive mitochondrial features, and mitochondria in dauer muscles exhibit unique reticulum‐like structure. It is proposed that these specialized mitochondria structures may serve as an adaptive mechanism to support stage‐specific behavioral and physiological needs.https://doi.org/10.1002/advs.202411191C. elegansdeep learningdevelopmentelectron microscopyfluorescence imagingmitochondria
spellingShingle J. Alexander Bae
Myung‐kyu Choi
Soungyub Ahn
Gwanho Ko
Daniel T. Choe
Hyunsoo Yim
Ken C. Nguyen
Jinseop S. Kim
David H. Hall
Junho Lee
Structural Diversity of Mitochondria in the Neuromuscular System across Development Revealed by 3D Electron Microscopy
Advanced Science
C. elegans
deep learning
development
electron microscopy
fluorescence imaging
mitochondria
title Structural Diversity of Mitochondria in the Neuromuscular System across Development Revealed by 3D Electron Microscopy
title_full Structural Diversity of Mitochondria in the Neuromuscular System across Development Revealed by 3D Electron Microscopy
title_fullStr Structural Diversity of Mitochondria in the Neuromuscular System across Development Revealed by 3D Electron Microscopy
title_full_unstemmed Structural Diversity of Mitochondria in the Neuromuscular System across Development Revealed by 3D Electron Microscopy
title_short Structural Diversity of Mitochondria in the Neuromuscular System across Development Revealed by 3D Electron Microscopy
title_sort structural diversity of mitochondria in the neuromuscular system across development revealed by 3d electron microscopy
topic C. elegans
deep learning
development
electron microscopy
fluorescence imaging
mitochondria
url https://doi.org/10.1002/advs.202411191
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