Picower Institute of Learning and Memory, Massachusetts Institute of Technology, Cambridge, United States.
Department of Neuroscience, Cleveland Clinic Lerner Research Institute, Cleveland, United States.
Elife. 2022 Jul 29;11:e78079. doi: 10.7554/eLife.78079.
Human cerebral organoids are unique in their development of progenitor-rich zones akin to ventricular zones from which neuronal progenitors differentiate and migrate radially. Analyses of cerebral organoids thus far have been performed in sectioned tissue or in superficial layers due to their high scattering properties. Here, we demonstrate label-free three-photon imaging of whole, uncleared intact organoids (~2 mm depth) to assess early events of early human brain development. Optimizing a custom-made three-photon microscope to image intact cerebral organoids generated from Rett Syndrome patients, we show defects in the ventricular zone volumetric structure of mutant organoids compared to isogenic control organoids. Long-term imaging live organoids reveals that shorter migration distances and slower migration speeds of mutant radially migrating neurons are associated with more tortuous trajectories. Our label-free imaging system constitutes a particularly useful platform for tracking normal and abnormal development in individual organoids, as well as for screening therapeutic molecules via intact organoid imaging.
人类大脑类器官在其祖细胞丰富区的发育方面具有独特性,类似于从中分化和径向迁移神经元祖细胞的脑室区。由于其高散射特性,迄今为止对大脑类器官的分析都是在切片组织或浅层进行的。在这里,我们展示了未经处理的完整未切片类器官(~2 毫米深)的无标记三光子成像,以评估早期人类大脑发育的早期事件。通过优化定制的三光子显微镜对源自雷特综合征患者的未处理完整大脑类器官进行成像,我们发现与同基因对照类器官相比,突变体类器官的脑室区体积结构存在缺陷。对活类器官的长期成像显示,突变体径向迁移神经元的较短迁移距离和较慢的迁移速度与更曲折的轨迹相关。我们的无标记成像系统构成了一个特别有用的平台,可用于跟踪单个类器官的正常和异常发育,以及通过完整类器官成像筛选治疗分子。