从人类iPSC中导向神经元的差异化,用于模拟神经系统疾病
Cheng Wang1, Jonas Cerneckis1,2, Yanhong Shi3,4
1Department of Neurodegenerative Diseases, Beckman Research Institute of City of Hope, Duarte, CA, USA.
Methods in molecular biology (Clifton, N.J.)
|April 17, 2024
概括
人类诱导的多能干细胞 (hiPSCs) 现在可以使用特定的转录因子可靠地分化为神经元. 这种方法提高了体外人类疾病建模的可复制性.
科学领域:
- 干细胞生物学 干细胞生物学
- 神经科学是一个神经科学.
- 生物技术是生物技术.
背景情况:
- 人类诱导的多能干细胞 (hiPSCs) 对于体外疾病建模至关重要.
- 人类初级神经元很难进入,动物模型显示了特定物种的差异.
- 由hiPSC衍生的神经元为研究人类神经元生物学提供了有价值的替代方案.
研究的目的:
- 提供一种可复制的方法,用于从hiPSCs中导向神经元分化.
- 为了利用转录因子驱动的差异化来控制人类神经元的产生.
- 为了提高hiPSC衍生的神经元用于疾病建模的实用性.
主要方法:
- 导向地将hiPSCs分化为神经前代细胞 (NPC).
- 神经原蛋白2 (NGN2) 和achaete-acute同源1 (ASCL1) 的多西环素诱导表达.
- 在NPC分化和lentiviral转导中最大限度地减少批量对批量的变化.
主要成果:
- 人类神经元与hiPSCs的快速和可控的分化.
- 通过NPC中间体成功生成神经元.
- 在人类神经元分化协议中提高可重现性.
结论:
- 描述的方法使得高效和可重复生成的hiPSC衍生的神经元.
- 这种方法促进了基于人类细胞的强大疾病建模.
- 转录因子驱动的差异化为神经科学研究提供了一个可扩展的解决方案.
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