Chemical & Biomolecular Engineering Department, North Carolina State University, Campus Box 7905, Raleigh, NC 27695, USA.
Cells. 2022 Apr 21;11(9):1411. doi: 10.3390/cells11091411.
Gene desensitization in response to a repeated stimulus is a complex phenotype important across homeostatic and disease processes, including addiction, learning, and memory. These complex phenotypes are being characterized and connected to important physiologically relevant functions in rodent systems but are difficult to capture in human models where even acute responses to important neurotransmitters are understudied. Here through transcriptomic analysis, we map the dynamic responses of human stem cell-derived medium spiny neuron-like cells (hMSN-like cells) to dopamine. Furthermore, we show that these human neurons can reflect and capture cellular desensitization to chronic versus acute administration of dopamine. These human cells are further able to capture complex receptor crosstalk in response to the pharmacological perturbations of distinct dopamine receptor subtypes. This study demonstrates the potential utility and remaining challenges of using human stem cell-derived neurons to capture and study the complex dynamic mechanisms of the brain.
基因对重复刺激的脱敏反应是一种复杂的表型,在稳态和疾病过程中都很重要,包括成瘾、学习和记忆。这些复杂的表型正在被描述,并与啮齿动物系统中重要的生理相关功能相关联,但在人类模型中很难捕捉到,因为即使是对重要神经递质的急性反应也研究不足。在这里,我们通过转录组分析,绘制了人类干细胞衍生的中脑多巴胺能神经元样细胞(hMSN-like cells)对多巴胺的动态反应图谱。此外,我们还表明,这些人类神经元可以反映和捕捉多巴胺慢性与急性给药后细胞的脱敏现象。这些人类细胞还能够捕捉到对不同多巴胺受体亚型的药理学干扰的复杂受体串扰。这项研究表明,使用人类干细胞衍生的神经元来捕捉和研究大脑复杂的动态机制具有潜在的应用价值和仍然存在的挑战。