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联合小分子处理加速人多能干细胞源性神经元的成熟。

Combined small-molecule treatment accelerates maturation of human pluripotent stem cell-derived neurons.

机构信息

The Center for Stem Cell Biology, Sloan-Kettering Institute for Cancer Research, New York, NY, USA.

Developmental Biology Program, Sloan-Kettering Institute for Cancer Research, New York, NY, USA.

出版信息

Nat Biotechnol. 2024 Oct;42(10):1515-1525. doi: 10.1038/s41587-023-02031-z. Epub 2024 Jan 2.

Abstract

The maturation of human pluripotent stem cell (hPSC)-derived neurons mimics the protracted timing of human brain development, extending over months to years for reaching adult-like function. Prolonged in vitro maturation presents a major challenge to stem cell-based applications in modeling and treating neurological disease. Therefore, we designed a high-content imaging assay based on morphological and functional readouts in hPSC-derived cortical neurons which identified multiple compounds that drive neuronal maturation including inhibitors of lysine-specific demethylase 1 and disruptor of telomerase-like 1 and activators of calcium-dependent transcription. A cocktail of four factors, GSK2879552, EPZ-5676, N-methyl-D-aspartate and Bay K 8644, collectively termed GENtoniK, triggered maturation across all parameters tested, including synaptic density, electrophysiology and transcriptomics. Maturation effects were further validated in cortical organoids, spinal motoneurons and non-neural lineages including melanocytes and pancreatic β-cells. The effects on maturation observed across a broad range of hPSC-derived cell types indicate that some of the mechanisms controlling the timing of human maturation might be shared across lineages.

摘要

人类多能干细胞(hPSC)衍生神经元的成熟过程模拟了人类大脑发育的漫长时间,需要数月至数年才能达到成人样功能。体外长时间成熟是基于干细胞的神经疾病建模和治疗应用的主要挑战。因此,我们设计了一种基于 hPSC 衍生皮质神经元形态和功能读数的高内涵成像测定法,该方法确定了多种化合物可促进神经元成熟,包括赖氨酸特异性去甲基酶 1 的抑制剂、端粒酶样 1 的破坏剂和钙依赖性转录的激活剂。四种因子(GSK2879552、EPZ-5676、N-甲基-D-天冬氨酸和 Bay K 8644)的混合物,统称为 GENtoniK,可触发所有测试参数的成熟,包括突触密度、电生理学和转录组学。在皮质类器官、脊髓运动神经元和非神经谱系(包括黑素细胞和胰岛β细胞)中进一步验证了成熟效应。在广泛的 hPSC 衍生细胞类型中观察到的成熟效应表明,控制人类成熟时间的一些机制可能在谱系间共享。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b063/11471552/a3ac9059d079/41587_2023_2031_Fig1_HTML.jpg

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