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细胞外包被基质对人诱导多能干细胞向皮质神经元分化的系统评价

Systematic Evaluation of Extracellular Coating Matrix on the Differentiation of Human-Induced Pluripotent Stem Cells to Cortical Neurons.

作者信息

Li Siyao, Liu Yan, Luo Xianyang, Hong Wei

机构信息

Shenzhen Key Laboratory of Neuroimmunomodulation for Neurological Diseases, Shenzhen-Hong Kong Institute of Brain Science, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen 518055, China.

出版信息

Int J Mol Sci. 2024 Dec 30;26(1):230. doi: 10.3390/ijms26010230.

Abstract

Induced pluripotent stem cell (iPSC)-derived neurons (iNs) have been widely used as models of neurodevelopment and neurodegenerative diseases. Coating cell culture vessels with extracellular matrixes (ECMs) gives structural support and facilitates cell communication and differentiation, ultimately enhances neuronal functions. However, the relevance of different ECMs to the natural environment and their impact on neuronal differentiation have not been fully characterized. In this study, we report the use of four commonly used extracellular matrixes, poly-D-lysine (PDL), poly-L-ornithine (PLO), Laminin and Matrigel, which we applied to compare the single-coating and double-coating conditions on iNs differentiation and maturation. Using the IncuCyte live-cell imaging system, we found that iNs cultured on single Matrigel- and Laminin-coated vessels have significantly higher density of neurite outgrowth and branch points than PLO or PDL but produce abnormal highly straight neurite outgrowth and larger cell body clumps. All the four double-coating conditions significantly reduced the clumping of neurons, in which the combination of PDL+Matrigel also enhanced neuronal purity. Double coating with PDL+Matrigel also tended to improve dendritic and axonal development and the distribution of pre and postsynaptic markers. These results demonstrate that the extracellular matrix contributes to the differentiation of cultured neurons and that double coating with PDL+Matrigel gives the best outcomes. Our study indicates that neuronal differentiation and maturation can be manipulated, to a certain extent, by adjusting the ECM recipe, and provides important technical guidance for the use of the ECM in neurological studies.

摘要

诱导多能干细胞(iPSC)衍生的神经元(iNs)已被广泛用作神经发育和神经退行性疾病的模型。用细胞外基质(ECM)包被细胞培养容器可提供结构支持,促进细胞通讯和分化,最终增强神经元功能。然而,不同ECM与自然环境的相关性及其对神经元分化的影响尚未完全明确。在本研究中,我们报告了使用四种常用的细胞外基质:聚-D-赖氨酸(PDL)、聚-L-鸟氨酸(PLO)、层粘连蛋白和基质胶,我们将其用于比较单包被和双包被条件对iNs分化和成熟的影响。使用IncuCyte活细胞成像系统,我们发现,在单基质胶和层粘连蛋白包被的容器上培养的iNs,其神经突生长密度和分支点明显高于PLO或PDL,但会产生异常的高度笔直的神经突生长和更大的细胞体团块。所有四种双包被条件均显著减少了神经元的聚集,其中PDL+基质胶的组合还提高了神经元纯度。PDL+基质胶双包被也倾向于改善树突和轴突发育以及突触前和突触后标记物的分布。这些结果表明,细胞外基质有助于培养神经元的分化,并且PDL+基质胶双包被产生的效果最佳。我们的研究表明,通过调整ECM配方,可在一定程度上操控神经元的分化和成熟,并为神经学研究中ECM的使用提供了重要的技术指导。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ddbe/11720352/38ab955612d1/ijms-26-00230-g001.jpg

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