Interspecies chimerism with human embryonic stem cells generates functional human dopamine neurons at low efficiency.

Interspecies chimeras offer great potential for regenerative medicine and the creation of human disease models. Whether human pluripotent stem cell-derived neurons in an interspecies chimera can differentiate into functional neurons and integrate into host neural circuity is not known. Here, we show, using Engrailed 1 (En1) as a development niche, that human naive-like embryonic stem cells (ESCs) can incorporate into embryonic and adult mouse brains. Human-derived neurons including tyrosine hydroxylase (TH)+ neurons integrate into the mouse brain at low efficiency. These TH+ neurons have electrophysiologic properties consistent with their human origin. In addition, these human-derived neurons in the mouse brain accumulate pathologic phosphorylated α-synuclein in response to α-synuclein preformed fibrils. Optimization of human/mouse chimeras could be used to study human neuronal differentiation and human brain disorders. Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.

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Hu Wang, Xiling Yin, Jinchong Xu, Li Chen, Senthilkumar S Karuppagounder, Enquan Xu, Xiaobo Mao, Valina L Dawson, Ted M Dawson. Interspecies chimerism with human embryonic stem cells generates functional human dopamine neurons at low efficiency. Stem cell reports. 2024 Jan 09;19(1):54-67

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PMID: 38134925

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