Answers are grounded in this paper and cite their sources.
Cellular morphology, a critical manifestation of biological characteristics, is linked to functions. In traditional cell detection, invasive labeling and detection methods not only compromise cellular viability but also entail labor-intensive workflows. Here we presented a non-invasive artificial intelligence framework that integrated deep learning (DL) and machine learning (ML) to predict the immunomodulatory capacity of mesenchymal stem cells (MSCs) through morphological profiling. The improved PreAct-ResNet50 encoder-decoder architecture was used to achieve high-accuracy instance segmentation of cells and nuclei, enabling quantification of morphological features. A LightGBM-based predictive model was subsequently employed to predict MSCs immunomodulatory biomarkers through morphological features. This dual-model system demonstrated satisfactory cell segmentation and biological characteristics prediction capabilities through performance testing. Our method provided an efficient, non- invasive tool for real-time MSCs potency assessment, which could enhance quality controls in cell therapy manufacturing.
No takes yet. Share an insight, caveat, or question.
Liu et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: