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通过机器学习分析剪切介导的血小板黏附运动学的体外测量。

In Vitro Measurements of Shear-Mediated Platelet Adhesion Kinematics as Analyzed through Machine Learning.

机构信息

Department of Biomedical Engineering, T08-50 Health Sciences Center, Stony Brook University, Stony Brook, NY, 11794-8084, USA.

Department of Applied Mathematics and Statistics, Stony Brook University, Stony Brook, NY, USA.

出版信息

Ann Biomed Eng. 2021 Dec;49(12):3452-3464. doi: 10.1007/s10439-021-02790-3. Epub 2021 May 10.

DOI:10.1007/s10439-021-02790-3
PMID:33973127
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8578579/
Abstract

Platelet adhesion to blood vessel walls in shear flow is essential to initiating the blood coagulation cascade and prompting clot formation in vascular disease processes and prosthetic cardiovascular devices. Validation of predictive adhesion kinematics models at the single platelet level is difficult due to gaps in high resolution, dynamic morphological data or a mismatch between simulation and experimental parameters. Gel-filtered platelets were perfused at 30 dyne/cm in von Willebrand Factor (vWF)-coated microchannels, with flipping platelets imaged at high spatial and temporal resolution. A semi-unsupervised learning system (SULS), consisting of a series of convolutional neural networks, was used to segment platelet geometry, which was compared with expert-analyzed images. Resulting time-dependent rotational angles were smoothed with wavelet-denoising and shifting techniques to characterize the rotational period and quantify flipping kinematics. We observed that flipping platelets do not follow the previously-modeled modified Jefferey orbit, but are characterized by a longer lift-off and shorter reattachment period. At the juncture of the two periods, rotational velocity approached 257.48 ± 13.31 rad/s. Our SULS approach accurately segmented large numbers of moving platelet images to identify distinct adhesive kinematic characteristics which may further validate the physical accuracy of individual platelet motion in multiscale models of shear-mediated thrombosis.

摘要

血小板在切变流中黏附于血管壁,对于启动血液凝固级联反应以及在血管疾病过程和人工心血管设备中促使血栓形成至关重要。由于高分辨率动态形态数据的差距或模拟与实验参数之间不匹配,在单个血小板水平上验证预测黏附运动学模型具有一定难度。在 von Willebrand 因子 (vWF) 涂层的微通道中,以 30 达因/厘米的剪切力使凝胶过滤后的血小板灌注,以高时空分辨率对翻转的血小板进行成像。一个由一系列卷积神经网络组成的半监督学习系统 (SULS) 用于分割血小板的几何形状,并将其与专家分析的图像进行比较。所得到的时变旋转角度通过小波去噪和移位技术进行平滑处理,以表征旋转周期并量化翻转运动学。我们观察到,翻转的血小板并不遵循之前建模的改良 Jeffrey 轨道,而是具有更长的升离和更短的重新附着周期。在两个周期的交界处,旋转速度接近 257.48 ± 13.31 rad/s。我们的 SULS 方法准确地分割了大量移动的血小板图像,以识别出独特的黏附运动学特征,这可能进一步验证了多尺度剪切介导血栓形成模型中单个血小板运动的物理准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/206cff0d8c2a/nihms-1750186-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/8a6afc7412ac/nihms-1750186-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/349d4862955f/nihms-1750186-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/b6dcb387fcd4/nihms-1750186-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/d11ab93c15d2/nihms-1750186-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/6251879e650b/nihms-1750186-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/206cff0d8c2a/nihms-1750186-f0006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/8a6afc7412ac/nihms-1750186-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/349d4862955f/nihms-1750186-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/b6dcb387fcd4/nihms-1750186-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/d11ab93c15d2/nihms-1750186-f0004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/6251879e650b/nihms-1750186-f0005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d27e/8578579/206cff0d8c2a/nihms-1750186-f0006.jpg

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