Cullen D Kacy, Gordián-Vélez Wisberty J, Struzyna Laura A, Jgamadze Dennis, Lim James, Wofford Kathryn L, Browne Kevin D, Chen H Isaac
Center for Brain Injury & Repair, Department of Neurosurgery, Perelman School of Medicine, University of Pennsylvania, 105E Hayden Hall/3320 Smith Walk, 3rd Floor, Silverstein Pavilion/3400 Spruce Street, Philadelphia, PA 19104, USA; Center for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA 19104, USA; Department of Bioengineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA 19104, USA.
Center for Brain Injury & Repair, Department of Neurosurgery, Perelman School of Medicine, University of Pennsylvania, 105E Hayden Hall/3320 Smith Walk, 3rd Floor, Silverstein Pavilion/3400 Spruce Street, Philadelphia, PA 19104, USA; Center for Neurotrauma, Neurodegeneration & Restoration, Corporal Michael J. Crescenz Veterans Affairs Medical Center, Philadelphia, PA 19104, USA; Department of Bioengineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA 19104, USA.
iScience. 2019 Nov 22;21:57-67. doi: 10.1016/j.isci.2019.10.004. Epub 2019 Oct 3.
Reestablishing cerebral connectivity is a critical part of restoring neuronal network integrity and brain function after trauma, stroke, and neurodegenerative diseases. Creating transplantable axon tracts in the laboratory is an unexplored strategy for overcoming the common barriers limiting axon regeneration in vivo, including growth-inhibiting factors and the limited outgrowth capacity of mature neurons in the brain. We describe the generation, phenotype, and connectivity of constrained three-dimensional human axon tracts derived from brain organoids. These centimeter-long constructs are encased in an agarose shell that permits physical manipulation and are composed of discrete cellular regions spanned by axon tracts, mirroring the separation of cerebral gray and white matter. Features of cerebral cortex also are emulated, as evidenced by the presence of neurons with different cortical layer phenotypes. This engineered neural tissue represents a first step toward potentially reconstructing brain circuits by physically replacing neuronal populations and long-range axon tracts in the brain.
重建大脑连通性是创伤、中风和神经退行性疾病后恢复神经网络完整性和脑功能的关键部分。在实验室中创建可移植的轴突束是一种尚未探索的策略,用于克服限制体内轴突再生的常见障碍,包括生长抑制因子和大脑中成熟神经元有限的生长能力。我们描述了源自脑类器官的受限三维人类轴突束的生成、表型和连通性。这些厘米长的结构包裹在琼脂糖外壳中,便于物理操作,由轴突束跨越的离散细胞区域组成,反映了脑灰质和白质的分离。大脑皮层的特征也得到了模拟,不同皮层层表型的神经元的存在证明了这一点。这种工程化神经组织代表了通过物理替换大脑中的神经元群体和长距离轴突束来潜在重建脑回路的第一步。