Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA.
Human Brain Organogenesis Program, Stanford University, Stanford, CA, USA.
Nat Biotechnol. 2020 Dec;38(12):1421-1430. doi: 10.1038/s41587-020-00763-w. Epub 2020 Dec 3.
Cortico-striatal projections are critical components of forebrain circuitry that regulate motivated behaviors. To enable the study of the human cortico-striatal pathway and how its dysfunction leads to neuropsychiatric disease, we developed a method to convert human pluripotent stem cells into region-specific brain organoids that resemble the developing human striatum and include electrically active medium spiny neurons. We then assembled these organoids with cerebral cortical organoids in three-dimensional cultures to form cortico-striatal assembloids. Using viral tracing and functional assays in intact or sliced assembloids, we show that cortical neurons send axonal projections into striatal organoids and form synaptic connections. Medium spiny neurons mature electrophysiologically following assembly and display calcium activity after optogenetic stimulation of cortical neurons. Moreover, we derive cortico-striatal assembloids from patients with a neurodevelopmental disorder caused by a deletion on chromosome 22q13.3 and capture disease-associated defects in calcium activity, showing that this approach will allow investigation of the development and functional assembly of cortico-striatal connectivity using patient-derived cells.
皮质纹状体投射是调节动机行为的前脑回路的关键组成部分。为了能够研究人类皮质纹状体通路以及其功能障碍如何导致神经精神疾病,我们开发了一种将人类多能干细胞转化为具有类似于发育中的人类纹状体的区域特异性脑类器官的方法,其中包括电活性的中间多棘神经元。然后,我们将这些类器官与大脑皮质类器官在三维培养物中组装在一起,形成皮质纹状体联合体。使用完整或切片联合体中的病毒追踪和功能测定,我们表明皮质神经元将轴突投射到纹状体类器官中并形成突触连接。中间多棘神经元在组装后在电生理学上成熟,并在皮质神经元的光遗传学刺激后显示钙活性。此外,我们从由染色体 22q13.3 缺失引起的神经发育障碍患者中获得皮质纹状体联合体,并捕获钙活性的疾病相关缺陷,表明这种方法将允许使用患者来源的细胞研究皮质纹状体连接的发育和功能组装。