Generating human neural diversity with a multiplexed morphogen screen in organoids

IF 19.8 1区 医学 Q1 CELL & TISSUE ENGINEERING
Neal D. Amin, Kevin W. Kelley, Konstantin Kaganovsky, Massimo Onesto, Jin Hao, Yuki Miura, James P. McQueen, Noah Reis, Genta Narazaki, Tommy Li, Shravanti Kulkarni, Sergey Pavlov, Sergiu P. Pașca
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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.

Abstract Image

在类器官中使用多路形态原筛选产生人类神经多样性
在发育中的神经系统中,形态原编排了显著的细胞多样性的产生。干细胞在体外的分化往往依赖于这些信号通路的组合调节。然而,缺乏系统的方法来理解形态导向的分化已经排除了许多神经细胞群体的产生,区域规范和成熟的一般原则仍然不完整。在这里,我们在培养超过70天的人类神经类器官中开发了14种形态因子的阵列筛选。单细胞多路RNA测序数据的反褶积揭示了脑区规范的设计原则。我们调整神经亚型多样性,在组装体中产生一种表达速激肽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,我们使用新生大鼠移植策略,使人类浦肯野神经元发展出其标志性的复杂树突分支。这个综合的平台可以深入了解影响干细胞来源的神经多样化和成熟的因素。
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来源期刊
Cell stem cell
Cell stem cell 生物-细胞生物学
CiteScore
37.10
自引率
2.50%
发文量
151
审稿时长
42 days
期刊介绍: Cell Stem Cell is a comprehensive journal covering the entire spectrum of stem cell biology. It encompasses various topics, including embryonic stem cells, pluripotency, germline stem cells, tissue-specific stem cells, differentiation, epigenetics, genomics, cancer stem cells, stem cell niches, disease models, nuclear transfer technology, bioengineering, drug discovery, in vivo imaging, therapeutic applications, regenerative medicine, clinical insights, research policies, ethical considerations, and technical innovations. The journal welcomes studies from any model system providing insights into stem cell biology, with a focus on human stem cells. It publishes research reports of significant importance, along with review and analysis articles covering diverse aspects of stem cell research.
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