人ipsc衍生的神经元和少突胶质细胞共培养作为髓鞘形成的小分子筛选试验。

IF 1 Q3 BIOLOGY
Stefanie Elke Chie, Zsofia Szentpetery, Melanie Generali, Tanja Kuhlmann, Giancarlo Natalucci, Maria Consolata Miletta
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引用次数: 0

摘要

神经元和少突胶质细胞是大脑的组成部分。神经元形成突触连接并传递信号,而少突胶质细胞,包括少突胶质前体细胞(OPCs)及其衍生物,对中枢神经系统的维持和髓鞘形成至关重要。对人类特异性神经元-少突胶质细胞模型系统来研究这些相互作用的需求已经增长,但共培养方案仍然有限。该领域的最新进展提供了从人类诱导多能干细胞(hiPSC)中获得神经元和OPCs共培养的方法,每种方法都有其独特的优点和挑战。本研究提出了一种高效、可重复的方法来获得神经元和表达o4的少突胶质细胞,然后是一个简单的共培养系统,最大限度地减少星形胶质细胞分化,并确保稳健的神经元和少突胶质细胞群体。主要特点•可靠,稳定的一代神经元和o4表达少突胶质细胞在实际的时间框架内。•利用hipsc衍生的神经元和表达o4的少突胶质细胞共培养系统。•神经元和少突胶质细胞在共培养10天内成熟。图形概述图形概述。该图概述了准备、区分和分析阶段所涉及的顺序步骤。关键阶段包括神经祖细胞(npc)分别分化为表达o4的少突胶质细胞和神经元,然后将它们组合成共培养物,然后用于进一步的实验。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human iPSC-Derived Neuron and Oligodendrocyte Co-culture as a Small-Molecule Screening Assay for Myelination.

Neurons and oligodendrocytes are the building blocks of the brain. Neurons form synaptic connections and transmit signals, while oligodendrocytes, including oligodendrocyte precursor cells (OPCs) and their derivatives, are vital for central nervous system maintenance and myelination. The demand for human-specific neuron-oligodendrocyte model systems to study these interactions has grown, yet co-culture protocols remain limited. Recent advancements in the field provide methods for deriving co-cultures of neurons and OPCs from human induced pluripotent stem cells (hiPSC), each with distinct benefits and challenges. This study presents a time-efficient, reproducible method to derive neurons and O4-expressing oligodendrocytes, followed by a straightforward co-culture system that minimizes astrocyte differentiation and ensures robust neuron and oligodendrocyte populations. Key features • Reliable, stable generation of neurons and O4-expressing oligodendrocytes within a practical timeframe. • Co-culture system utilizing hIPSC-derived neurons and O4-expressing oligodendrocytes. • Maturation of neurons and oligodendrocytes achieved within 10 days of co-culturing. Graphical overview Graphical overview. The diagram outlines the sequential steps involved in the preparation, differentiation, and analysis phases. Key stages include the differentiation of neural progenitor cells (NPCs) into O4-expressing oligodendrocytes and neurons separately and then combining them into a co-culture, which can then be used for further experiments.

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CiteScore
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