ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025
Single Mitochondrion Morphology-Function Relationship Analysis Using Fluorescent Probes and Artificial Intelligence.
Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
3 citing papers in PubMed.
- Research on the Application of Fluorescent Probes in Revealing the Mechanism of Cerebral Ischemia-Reperfusion Injury.Chemical & biomedical imaging · 2026Review
- Investigating Mitochondrial Viscosity in Ferroptosis-Mediated Drug-Induced Liver Injury using a Double-Targeted Strategy.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
- Single Mitochondrion Morphology-Function Relationship Analysis Using Fluorescent Probes and Artificial Intelligence.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
10 authors.
Funding
Abstract
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.
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What Socratic holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.