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利用类器官中的多重形态发生素筛选生成人类神经多样性。

Generating human neural diversity with a multiplexed morphogen screen in organoids.

作者信息

Amin Neal D, Kelley Kevin W, Kaganovsky Konstantin, Onesto Massimo, Hao Jin, Miura Yuki, McQueen James P, Reis Noah, Narazaki Genta, Li Tommy, Kulkarni Shravanti, Pavlov Sergey, Pașca Sergiu P

机构信息

Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA; Stanford Brain Organogenesis Program, Wu Tsai Neuroscience Institute & Bio-X, Stanford, CA, USA.

Department of Psychiatry and Behavioral Sciences, Stanford University, Stanford, CA, USA; Stanford Brain Organogenesis Program, Wu Tsai Neuroscience Institute & Bio-X, Stanford, CA, USA.

出版信息

Cell Stem Cell. 2024 Dec 5;31(12):1831-1846.e9. doi: 10.1016/j.stem.2024.10.016.

Abstract

Morphogens choreograph the generation of remarkable cellular diversity in the developing nervous system. Differentiation of stem cells in vitro often relies upon the combinatorial modulation of these signaling pathways. However, the lack of a systematic approach to understand morphogen-directed differentiation has precluded the generation of many neural cell populations, and the general principles of regional specification and maturation remain incomplete. Here, we developed an arrayed screen of 14 morphogen modulators in human neural organoids cultured for over 70 days. Deconvolution of single-cell-multiplexed RNA sequencing data revealed design principles of brain region specification. We tuned neural subtype diversity to generate a tachykinin 3 (TAC3)-expressing striatal interneuron type within assembloids. To circumvent limitations of in vitro neuronal maturation, we used a neonatal rat transplantation strategy that enabled human Purkinje neurons to develop their hallmark complex dendritic branching. This comprehensive platform yields insights into the factors influencing stem cell-derived neural diversification and maturation.

摘要

形态发生素在发育中的神经系统中编排了显著的细胞多样性的产生。体外干细胞的分化通常依赖于这些信号通路的组合调控。然而,缺乏一种系统的方法来理解形态发生素导向的分化,阻碍了许多神经细胞群体的产生,并且区域特化和成熟的一般原则仍不完整。在这里,我们在培养超过70天的人类神经类器官中开发了一个包含14种形态发生素调节剂的阵列筛选。单细胞多重RNA测序数据的反卷积揭示了脑区特化的设计原则。我们调整神经亚型多样性,以在类组装体中产生表达速激肽3(TAC3)的纹状体中间神经元类型。为了规避体外神经元成熟的局限性,我们采用了新生大鼠移植策略,使人类浦肯野神经元能够发育出其标志性的复杂树突分支。这个综合平台深入了解了影响干细胞衍生神经多样化和成熟的因素。

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