Department of Computer Science and Engineering, Michigan State University, East Lansing, Michigan, USA.
Vascular Medicine Institute, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Magn Reson Med. 2017 Nov;78(5):1991-2002. doi: 10.1002/mrm.26571. Epub 2016 Dec 26.
Magnetic resonance imaging (MRI)-based cell tracking has emerged as a useful tool for identifying the location of transplanted cells, and even their migration. Magnetically labeled cells appear as dark contrast in T2*-weighted MRI, with sensitivities of individual cells. One key hurdle to the widespread use of MRI-based cell tracking is the inability to determine the number of transplanted cells based on this contrast feature. In the case of single cell detection, manual enumeration of spots in three-dimensional (3D) MRI in principle is possible; however, it is a tedious and time-consuming task that is prone to subjectivity and inaccuracy on a large scale. This research presents the first comprehensive study on how a computer-based intelligent, automatic, and accurate cell quantification approach can be designed for spot detection in MRI scans.
Magnetically labeled mesenchymal stem cells (MSCs) were transplanted into rats using an intracardiac injection, accomplishing single cell seeding in the brain. T2*-weighted MRI of these rat brains were performed where labeled MSCs appeared as spots. Using machine learning and computer vision paradigms, approaches were designed to systematically explore the possibility of automatic detection of these spots in MRI. Experiments were validated against known in vitro scenarios.
Using the proposed deep convolutional neural network (CNN) architecture, an in vivo accuracy up to 97.3% and in vitro accuracy of up to 99.8% was achieved for automated spot detection in MRI data.
The proposed approach for automatic quantification of MRI-based cell tracking will facilitate the use of MRI in large-scale cell therapy studies. Magn Reson Med 78:1991-2002, 2017. © 2016 International Society for Magnetic Resonance in Medicine.
基于磁共振成像(MRI)的细胞示踪已成为一种有用的工具,可以识别移植细胞的位置,甚至可以识别其迁移情况。经磁标记的细胞在 T2*-加权 MRI 中呈现为暗对比,具有单个细胞的灵敏度。基于 MRI 的细胞示踪广泛应用的一个关键障碍是无法根据这种对比特征确定移植细胞的数量。在单细胞检测的情况下,原则上可以对三维(3D)MRI 中的斑点进行手动计数;然而,这是一项繁琐且耗时的任务,在大规模情况下容易出现主观性和不准确性。本研究首次全面研究了如何设计基于计算机的智能、自动和准确的细胞定量方法,用于 MRI 扫描中的斑点检测。
使用心脏内注射将磁性标记的间充质干细胞(MSCs)移植到大鼠体内,在大脑中完成单细胞播种。对这些大鼠大脑进行 T2*-加权 MRI,标记的 MSCs 呈现为斑点。使用机器学习和计算机视觉范例,设计了方法来系统地探索在 MRI 中自动检测这些斑点的可能性。实验通过已知的体外情况进行了验证。
使用所提出的深度卷积神经网络(CNN)架构,在体内自动检测 MRI 数据中的斑点的准确率高达 97.3%,在体外的准确率高达 99.8%。
用于基于 MRI 的细胞示踪自动定量的方法将促进 MRI 在大规模细胞治疗研究中的应用。磁共振医学杂志 78:1991-2002, 2017。© 2016 国际磁共振学会。