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构建人脑类器官的协同工程方法。

A Synergistic Engineering Approach to Build Human Brain Spheroids.

作者信息

von Maydell Djuna, Jorfi Mehdi

机构信息

Center for Engineering in Medicine, Massachusetts General Hospital, Harvard Medical School, Charlestown, MA, USA.

出版信息

Methods Mol Biol. 2021;2258:151-169. doi: 10.1007/978-1-0716-1174-6_11.

Abstract

Self-assembling brain spheroids derived from human stem cells closely emulate the tangled connectivity of the human brain, recapitulate aspects of organized tissue structure, and are relatively easy to manipulate compared to other existing three-dimensional (3D) cellular models. However, current platforms generate heterogeneously sized and short-lived spheroids, which do not robustly and reproducibly model human brain development and diseases. Here, we present a method to generate large-scale arrays of homogeneously sized 3D brain spheroids derived from human-induced pluripotent stem cells (hiPSCs) or immortalized neural progenitor cells to recapitulate Alzheimer's disease (AD) pathology in vitro. When embedded in extracellular matrix, these brain spheroids develop extensive outward projection of neurites and form networks, which are mediated by thick bundles of dendrites. This array facilitates cost-effective, high-throughput drug screening and mechanistic studies to better understand human brain development and neurodegenerative conditions, such as AD .

摘要

源自人类干细胞的自组装脑球体紧密模拟人类大脑的复杂连接,概括组织结构的各个方面,并且与其他现有的三维(3D)细胞模型相比相对易于操作。然而,当前的平台会生成大小不均且寿命短暂的球体,无法可靠且可重复地模拟人类大脑发育和疾病。在此,我们提出一种方法,可从人诱导多能干细胞(hiPSC)或永生化神经祖细胞生成大规模、大小均匀的3D脑球体阵列,以在体外概括阿尔茨海默病(AD)病理。当嵌入细胞外基质时,这些脑球体发展出广泛的神经突向外投射并形成网络,这由厚束状树突介导。该阵列有助于进行经济高效的高通量药物筛选和机制研究,以更好地理解人类大脑发育和神经退行性疾病,如AD。

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