Generation of functional human serotonergic neurons from fibroblasts

被引:100
作者
Vadodaria, K. C. [1 ]
Mertens, J. [1 ]
Paquola, A. [1 ]
Bardy, C. [1 ]
Li, X. [1 ,2 ]
Jappelli, R. [1 ]
Fung, L. [1 ,2 ]
Marchetto, M. C. [1 ]
Hamm, M. [3 ]
Gorris, M. [1 ]
Koch, P. [4 ]
Gage, F. H. [1 ]
机构
[1] Salk Inst Biol Studies, Genet Lab, La Jolla, CA 92037 USA
[2] Univ Calif San Diego, San Diego UCSD, La Jolla, CA 92093 USA
[3] Salk Inst Biol Studies, La Jolla, CA 92037 USA
[4] Univ Bonn, Inst Reconstruct Neurobiol, Bonn, Germany
基金
瑞士国家科学基金会;
关键词
MOUSE EMBRYONIC STEM; DOPAMINERGIC-NEURONS; DIRECT CONVERSION; RAPHE NEURONS; HUMAN ES; CELLS; DIFFERENTIATION; SPECIFICATION; TRANSCRIPTION; INTERNEURONS;
D O I
10.1038/mp.2015.161
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The brain's serotonergic system centrally regulates several physiological processes and its dysfunction has been implicated in the pathophysiology of several neuropsychiatric disorders. While in the past our understanding of serotonergic neurotransmission has come mainly from mouse models, the development of pluripotent stem cell and induced fibroblast-to-neuron (iN) transdifferentiation technologies has revolutionized our ability to generate human neurons in vitro. Utilizing these techniques and a novel lentiviral reporter for serotonergic neurons, we identified and overexpressed key transcription factors to successfully generate human serotonergic neurons. We found that overexpressing the transcription factors NKX2.2, FEV, GATA2 and LMX1B in combination with ASCL1 and NGN2 directly and efficiently generated serotonergic neurons from human fibroblasts. Induced serotonergic neurons (iSNs) showed increased expression of specific serotonergic genes that are known to be expressed in raphe nuclei. iSNs displayed spontaneous action potentials, released serotonin in vitro and functionally responded to selective serotonin reuptake inhibitors (SSRIs). Here, we demonstrate the efficient generation of functional human serotonergic neurons from human fibroblasts as a novel tool for studying human serotonergic neurotransmission in health and disease.
引用
收藏
页码:49 / 61
页数:13
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