Tian Qiyuan, Ngamsombat Chanon, Lee Hong-Hsi, Berger Daniel R, Wu Yuelong, Fan Qiuyun, Bilgic Berkin, Li Ziyu, Novikov Dmitry S, Fieremans Els, Rosen Bruce R, Lichtman Jeff W, Huang Susie Y
School of Biomedical Engineering, Tsinghua University, Beijing, PR China; Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Charlestown, MA, USA; Harvard Medical School, Boston, MA, USA.
Athinoula A. Martinos Center for Biomedical Imaging, Department of Radiology, Massachusetts General Hospital, Charlestown, MA, USA; Department of Radiology, Faculty of Medicine, Siriraj Hospital, Mahidol University, Thailand.
Neuroimage. 2025 Jun;313:121212. doi: 10.1016/j.neuroimage.2025.121212. Epub 2025 Apr 11.
Short-range association fibers located in the superficial white matter play an important role in mediating higher-order cognitive function in humans. Detailed morphological characterization of short-range association fibers at the microscopic level promises to yield important insights into the axonal features driving cortico-cortical connectivity in the human brain yet has been difficult to achieve to date due to the challenges of imaging at nanometer-scale resolution over large tissue volumes. This work presents results from multi-beam scanning electron microscopy (EM) data acquired at 4 × 4 × 33 nm resolution in a volume of human superficial white matter measuring 200 × 200 × 112 μm, leveraging automated analysis methods. Myelin and myelinated axons were automatically segmented using deep convolutional neural networks (CNNs), assisted by transfer learning and dropout regularization techniques. A total of 128,285 myelinated axons were segmented, of which 70,321 and 2102 were longer than 10 and 100 μm, respectively. Marked local variations in diameter (i.e., beading) and direction (i.e., undulation) were observed along the length of individual axons. Myelinated axons longer than 10 μm had inner diameters around 0.5 µm, outer diameters around 1 µm, and g-ratios around 0.5. This work fills a gap in knowledge of axonal morphometry in the superficial white matter and provides a large 3D human EM dataset and accurate segmentation results for a variety of future studies in different fields.
位于浅表白质的短程联合纤维在介导人类高级认知功能中发挥着重要作用。在微观层面上对短程联合纤维进行详细的形态学表征,有望深入了解驱动人类大脑皮质-皮质连接的轴突特征,但由于在大组织体积上以纳米级分辨率成像存在挑战,迄今为止这一目标一直难以实现。这项工作展示了利用自动分析方法,在体积为200×200×112μm的人类浅表白质中以4×4×33nm分辨率获取的多束扫描电子显微镜(EM)数据的结果。利用深度卷积神经网络(CNN),并借助迁移学习和随机失活正则化技术,对髓磷脂和有髓轴突进行了自动分割。总共分割出128,285条有髓轴突,其中分别有70,321条和2102条轴突长度超过10μm和100μm。沿着单个轴突的长度观察到明显的局部直径变化(即串珠状)和方向变化(即波动)。长度超过10μm的有髓轴突内径约为0.5μm,外径约为1μm,g比值约为0.5。这项工作填补了浅表白质轴突形态测量学知识的空白,并为不同领域的各种未来研究提供了一个大型的三维人类EM数据集和准确的分割结果。
J Appl Clin Med Phys. 2025-8
2025-1
Commun Biol. 2021-2-10
Proc Natl Acad Sci U S A. 2020-12-29
Neuroimage. 2021-2-15
Commun Biol. 2020-7-7