arXiv:2504.08096physics.bio-phcs.AI2025-04被引 2

用最小作用量原理解析细胞发育的熵与信息规律

Cellular Development Follows the Path of Minimum Action

  • 将最小作用量与最大熵结合,用Transformer建模细胞发育路径
  • 量化熵产生、信息曲率和局部不可逆性,揭示发育不对称性
  • 提供可解释指标,适合研究细胞命运决定的生物物理学者

细胞发育遵循随机但有规则的轨迹,其内在原理仍不明确。本文提出细胞发育沿最小作用量路径进行,符合自然界动态系统的基本物理规律。我们构建了一种计算框架,利用最小作用量与最大熵之间的深层联系,采用Transformer架构对单细胞RNA序列数据中的发育过程进行建模。该方法可精确量化熵产生、信息流曲率及局部不可逆性,揭示发育不对称性。在统一框架下,我们提出可解释的度量:熵用于捕捉探索-利用权衡,曲率用于评估可塑性-弹性动态,熵产生用于表征去分化与转分化。我们在单细胞和胚胎发育数据集上验证了该方法,证明其能揭示隐藏的热力学与信息约束,塑造细胞命运决策。

原文摘要 · Abstract (English)

Cellular development follows a stochastic yet rule-governed trajectory, though the underlying principles remain elusive. Here, we propose that cellular development follows paths of least action, aligning with foundational physical laws that govern dynamic systems across nature. We introduce a computational framework that takes advantage of the deep connection between the principle of least action and maximum entropy to model developmental processes using Transformers architecture. This approach enables precise quantification of entropy production, information flow curvature, and local irreversibility for developmental asymmetry in single-cell RNA sequence data. Within this unified framework, we provide interpretable metrics: entropy to capture exploration-exploitation trade-offs, curvature to assess plasticity-elasticity dynamics, and entropy production to characterize dedifferentiation and transdifferentiation. We validate our method across both single-cell and embryonic development datasets, demonstrating its ability to reveal hidden thermodynamic and informational constraints shaping cellular fate decisions.

细胞发育最小作用量Transformer熵分析

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