Deep Learning of Position-Aligned Dynamic Cell Deformation Trajectories for Ovarian Cell Phenotyping in Hyperbolic Microchannels

变形(气象学) 生物系统 运动学 机械 流量(数学) 弹道 人工智能 化学 卷积神经网络 职位(财务) 微流控 深度学习 频道(广播) 微通道 计算机科学 宏 流速 动力学(音乐) 几何学 物理 图像处理 算法 计算机视觉 流体力学 入口
作者
Yi-Bo Hu,Xi-Lin Gao,Hong-Fei LI,Zhuo Yang,Shu-Song Huang,Yong-Jiang Li,Xu-Qu Hu
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:98 (42): 29863-29879
标识
DOI:10.1021/acs.analchem.6c05067
摘要

Cell deformation during microfluidic transport evolves continuously, whereas cell phenotyping commonly relies on geometric descriptors measured at one or a few predefined channel positions. Such fixed-position measurements capture selected deformation states but overlook how the cellular response progresses along the flow path. Combined with high-speed imaging, hyperbolic microchannels capture this progression as a continuous trajectory, enabling the shift from static morphological measurements to a dynamic response analysis. However, cell-to-cell differences in transit velocity cause equivalent image frames to represent different channel positions and hydrodynamic conditions, preventing a direct comparison of frame-indexed deformation trajectories. Here, we develop a trajectory-resolved framework that converts high-speed microfluidic image sequences into position-aligned dynamic cell deformation trajectories and uses deep learning to model their cell line-specific evolution for label-free ovarian cell phenotyping. Geometric and kinematic trajectories were extracted from three ovarian cancer cell lines (A2780, OVCAR-3, and SKOV-3) and one nonmalignant ovarian epithelial cell line (IOSE-80) at three flow rates. The trajectories were reparameterized by the axial position and resampled on a common spatial grid. Class-specific one-dimensional convolutional neural networks predicted downstream trajectories from the inlet state and flow conditions. An unknown cell was classified by comparing its measured trajectory with class-specific predictions, and prediction errors in the width, area, perimeter, and axial velocity were integrated by soft voting. The framework achieved 93.26% accuracy, 94.07% macro precision, 90.25% macro recall, and a 91.85% macro-F1 score on the held-out test data. These results support extending microfluidic cell phenotyping from isolated geometric states to the position-aligned analysis of dynamic deformation trajectories.
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