Machine learning multiscale collective cell dynamics: From single-cell characterization to multicellular monolayer modeling

• 成果类型: Article
• 署名作者: Xu, Kun; Bai, Jianbo; Zhang, Hao-Shun; Lv, Cheng-Lin; Li, Yue; Shao, Yue; Feng, Xi-Qiao; Li, Bo
• 署名单位: Tsinghua University; Tsinghua University; Tsinghua University
• 刊物名称: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
• ISSN/ISSBN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.2522744123
• 发表日期: 2026-04-28
• 页码: e2522744123
• 关键词: Machine learning; collective cell dynamics; physics-guided ML; multiscale dynamics; AI for science; migration; mechanics; forces; cancer; hidden; FLOW

摘要

Collective cell dynamics are fundamental to numerous physiological processes, including embryo development, tissue morphogenesis, immune response, and disease progression. Accurately modeling these dynamics across scales remains challenging, as traditional physics-based models usually rely on many unmeasurable parameters and unclear active physics, limiting their ability to capture both single-cell features and emergent multicellular behaviors. Here, we introduce a scale-adaptive hybrid machine learning (ML) framework, in which complementary physics-guided and physics-agnostic method each resolves an above key issue at single-cell and multicellular scales, respectively. The physics-guided ML method integrates physical models with experimental data to infer previously unmeasurable parameters, enabling more accurate characterization of single-cell shape and velocity features, but unknown active forces and inherent physical assumptions still constrain its ability to predict multicellular scale dynamics. In contrast, the physics-agnostic ML method bypasses explicit physical assumptions to directly model multicellular behaviors from historical state sequences. This method provides robust long-term predictions of coarse-grained density oscillations and waves observed experimentally, yet it suffers from high stochasticity when applied to single-cell scale modeling. By assigning each approach to the scale where it is most effective, our framework leverages their respective strengths while mitigating their limitations. This complementary strategy bridges the gap between theoretical modeling and experimental observations, offering a versatile computational paradigm for multiscale collective cell dynamics with broad potential in diverse physiological and pathological contexts.