TY - JOUR
T1 - Single Mitochondrion Morphology-Function Relationship Analysis Using Fluorescent Probes and Artificial Intelligence
AU - Ding, Yang
AU - Fang, Bin
AU - Li, Qingzhe
AU - Zhang, Biying
AU - Li, Jintao
AU - Bai, Hua
AU - Voelcker, Nicolas H.
AU - Peng, Bo
AU - Yang, Xuekang
AU - Li, Lin
N1 - Publisher Copyright:
© 2025 The Author(s). Advanced Science published by Wiley-VCH GmbH.
PY - 2025/11/20
Y1 - 2025/11/20
N2 - The ability to decode the relationship between mitochondrial morphology and function at the level of individual organelles is central to understanding cellular responses to stress, such as hypoxia. Herein, a comprehensive strategy is presented that integrates tailored fluorescent probes with artificial intelligence (AI) for single mitochondrion analysis. Focus is on three interrelated biomarkers, reactive oxygen species (ROS), viscosity, and mitochondrial membrane potential (MMP), that together form a pathophysiological axis indicative of mitochondrial state under hypoxic stress. A functional probe set is used to image these features simultaneously, including a newly developed dual-cationic probe, MitoVP, which enhances mitochondrial targeting and resolution for viscosity sensing. Mitochondrial morphological features are then extracted using a deep learning-based algorithm, which further classified individual mitochondria into dot, rod, and network morphotypes. This analysis enabled quantitative mapping between mitochondrial morphology and functional states, revealing significant heterogeneity across diverse physiological conditions. Based on this characterization, a random forest classifier trained on over 10,000 mitochondria accurately distinguished normoxic from hypoxic states and identified viscosity as a primary contributor to mitochondrial status under hypoxia. This integrated approach provides a powerful platform for single organelle investigations and advances the understanding of mitochondrial dysfunction in complex biological systems.
AB - The ability to decode the relationship between mitochondrial morphology and function at the level of individual organelles is central to understanding cellular responses to stress, such as hypoxia. Herein, a comprehensive strategy is presented that integrates tailored fluorescent probes with artificial intelligence (AI) for single mitochondrion analysis. Focus is on three interrelated biomarkers, reactive oxygen species (ROS), viscosity, and mitochondrial membrane potential (MMP), that together form a pathophysiological axis indicative of mitochondrial state under hypoxic stress. A functional probe set is used to image these features simultaneously, including a newly developed dual-cationic probe, MitoVP, which enhances mitochondrial targeting and resolution for viscosity sensing. Mitochondrial morphological features are then extracted using a deep learning-based algorithm, which further classified individual mitochondria into dot, rod, and network morphotypes. This analysis enabled quantitative mapping between mitochondrial morphology and functional states, revealing significant heterogeneity across diverse physiological conditions. Based on this characterization, a random forest classifier trained on over 10,000 mitochondria accurately distinguished normoxic from hypoxic states and identified viscosity as a primary contributor to mitochondrial status under hypoxia. This integrated approach provides a powerful platform for single organelle investigations and advances the understanding of mitochondrial dysfunction in complex biological systems.
KW - artificial intelligence
KW - fluorescent probes
KW - image segmentation
KW - mitochondria
KW - single mitochondrion analysis
UR - https://www.scopus.com/pages/publications/105013786510
U2 - 10.1002/advs.202509140
DO - 10.1002/advs.202509140
M3 - 文章
AN - SCOPUS:105013786510
SN - 2198-3844
VL - 12
JO - Advanced Science
JF - Advanced Science
IS - 43
M1 - e09140
ER -