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通过无创体积成像对大规模人类大脑类器官中神经和少突胶质细胞发育进行长期追踪。

Long-term tracking of neural and oligodendroglial development in large-scale human cerebral organoids by noninvasive volumetric imaging.

作者信息

Park Sangjun, Min Cheol Hong, Choi Eunjin, Choi Jeong-Sun, Park Kyungjin, Han Seokyoung, Choi Wonjun, Jang Hyun-Jong, Cho Kyung-Ok, Kim Moonseok

机构信息

Department of Medical Life Sciences, College of Medicine, The Catholic University of Korea, Seoul, 06591, Korea.

Department of Medical Sciences, College of Medicine, The Catholic University of Korea, Seoul, 06591, Korea.

出版信息

Sci Rep. 2025 Jan 20;15(1):2536. doi: 10.1038/s41598-025-85455-8.

DOI:10.1038/s41598-025-85455-8
PMID:39833280
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11747076/
Abstract

Human cerebral organoids serve as a quintessential model for deciphering the complexities of brain development in a three-dimensional milieu. However, imaging these organoids, particularly when they exceed several millimeters in size, has been curtailed by the technical impediments such as phototoxicity, slow imaging speeds, and inadequate resolution and imaging depth. Addressing these pivotal challenges, our study has pioneered a high-speed scanning microscope, synergistically coupled with advanced computational image processing. This ensemble has empowered us to monitor the intricate dynamics of neuron and oligodendrocyte development within cerebral organoids across a trajectory of approximately two months. Line-shaped illumination mitigates photodamage and, alongside refined spatial gating, maximizes signal collection through integrating with computational processing. The integration of deconvolution and compressive sensing has improved image contrast by 6-fold, elucidating fine features of the neurites. Thus, noninvasive imaging enabled us to perform long-term tracking of neural and oligodendroglial development in the large-scale human cerebral organoid. Furthermore, our sophisticated volumetric segmentation algorithm has yielded a robust four-dimensional quantitative analysis, encapsulating both neuronal and oligodendroglial maturation. Collectively, these advances mark a significant advancement in the field of neurodevelopment, providing a powerful tool for in-depth study of complex brain organoid systems.

摘要

人类大脑类器官是在三维环境中解读大脑发育复杂性的典型模型。然而,对这些类器官进行成像,尤其是当它们的大小超过几毫米时,受到了诸如光毒性、成像速度慢、分辨率和成像深度不足等技术障碍的限制。为应对这些关键挑战,我们的研究开创了一种高速扫描显微镜,并与先进的计算图像处理技术协同结合。这一组合使我们能够在大约两个月的时间内监测大脑类器官内神经元和少突胶质细胞发育的复杂动态。线形照明减轻了光损伤,并且与精细的空间门控一起,通过与计算处理相结合最大化了信号收集。去卷积和压缩感知的整合将图像对比度提高了6倍,阐明了神经突的精细特征。因此,无创成像使我们能够对大规模人类大脑类器官中的神经和少突胶质细胞发育进行长期跟踪。此外,我们复杂的体积分割算法产生了强大的四维定量分析,涵盖了神经元和少突胶质细胞的成熟过程。总的来说,这些进展标志着神经发育领域的重大进步,为深入研究复杂的脑类器官系统提供了一个强大的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/e845eb3dd7ac/41598_2025_85455_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/96ca9b8ba151/41598_2025_85455_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/33cd5e509047/41598_2025_85455_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/f642d58dbd78/41598_2025_85455_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/8f7d6df452da/41598_2025_85455_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/70557a37e0a2/41598_2025_85455_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/e845eb3dd7ac/41598_2025_85455_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/96ca9b8ba151/41598_2025_85455_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/33cd5e509047/41598_2025_85455_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/f642d58dbd78/41598_2025_85455_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/8f7d6df452da/41598_2025_85455_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/70557a37e0a2/41598_2025_85455_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8315/11747076/e845eb3dd7ac/41598_2025_85455_Fig6_HTML.jpg

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