| Literature DB >> 32083763 |
Tae Hwan Kwak1, Ji Hyun Kang1, Sai Hali1, Jonghun Kim1, Kee-Pyo Kim2, Chanhyeok Park3, Ju-Hyun Lee4, Ha Kyun Ryu5, Ji Eun Na4, Junghyun Jo6,7, Hyunsoo Shawn Je8, Huck-Hui Ng6, Jeongwoo Kwon9, Nam-Hyung Kim9, Kwon Ho Hong3, Woong Sun4, Chi Hye Chung5, Im Joo Rhyu4, Dong Wook Han10,11.
Abstract
Recent studies have demonstrated the generation of midbrain-like organoids (MOs) from human pluripotent stem cells. However, the low efficiency of MO generation and the relatively immature and heterogeneous structures of the MOs hinder the translation of these organoids from the bench to the clinic. Here we describe the robust generation of MOs with homogeneous distribution of midbrain dopaminergic (mDA) neurons. Our MOs contain not only mDA neurons but also other neuronal subtypes as well as functional glial cells, including astrocytes and oligodendrocytes. Furthermore, our MOs exhibit mDA neuron-specific cell death upon treatment with 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine, indicating that MOs could be a proper human model system for studying the in vivo pathology of Parkinson's disease (PD). Our optimized conditions for producing homogeneous and mature MOs might provide an advanced patient-specific platform for in vitro disease modeling as well as for drug screening for PD. ©AlphaMed Press 2020.Entities:
Keywords: Parkinson's disease; differentiation; embryonic stem cells (ESCs); neural differentiation
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Year: 2020 PMID: 32083763 DOI: 10.1002/stem.3163
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277