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Abstract

Investigating human oligodendrogenesis and the interaction of oligodendrocytes with neurons and astrocytes would accelerate our understanding of the mechanisms underlying white matter disorders. However, this is challenging because of the limited accessibility of functional human brain tissue. Here, we developed a new differentiation method of human induced pluripotent stem cells to generate three-dimensional brain organoids that contain oligodendrocytes as well as neurons and astrocytes, called human oligodendrocyte spheroids. We found that oligodendrocyte lineage cells derived in human oligodendrocyte spheroids transitioned through developmental stages similar to primary human oligodendrocytes and that the migration of oligodendrocyte lineage cells and their susceptibility to lysolecithin exposure could be captured by live imaging. Moreover, their morphology changed as they matured over time in vitro and started myelinating neurons. We anticipate that this method can be used to study oligodendrocyte development, myelination, and interactions with other major cell types in the CNS.

The authors generate 3D brain organoids containing oligodendrocytes, astrocytes, and neurons derived from human pluripotent stem cells. These human oligodendrocytes are transcriptionally similar to primary cells and mature to myelinate axons.

Details

Title
Differentiation and maturation of oligodendrocytes in human three-dimensional neural cultures
Author
Marton, Rebecca M 1   VIAFID ORCID Logo  ; Miura Yuki 2   VIAFID ORCID Logo  ; Sloan, Steven A 2 ; Li, Qingyun 3   VIAFID ORCID Logo  ; Revah Omer 2 ; Levy, Rebecca J 4 ; Huguenard, John R 4   VIAFID ORCID Logo  ; Pașca, Sergiu P 5   VIAFID ORCID Logo 

 Stanford University School of Medicine, Department of Psychiatry and Behavioral Sciences, Stanford, USA (GRID:grid.168010.e) (ISNI:0000000419368956); Stanford University School of Medicine, Program in Stem Cell Biology and Regenerative Medicine, Stanford, USA (GRID:grid.168010.e) (ISNI:0000000419368956) 
 Stanford University School of Medicine, Department of Psychiatry and Behavioral Sciences, Stanford, USA (GRID:grid.168010.e) (ISNI:0000000419368956) 
 Stanford University School of Medicine, Department of Neurobiology, Stanford, USA (GRID:grid.168010.e) (ISNI:0000000419368956) 
 Stanford University School of Medicine, Department of Neurology and Neurological Sciences, Stanford, USA (GRID:grid.168010.e) (ISNI:0000000419368956) 
 Stanford University School of Medicine, Department of Psychiatry and Behavioral Sciences, Stanford, USA (GRID:grid.168010.e) (ISNI:0000000419368956); Stanford University, Human Brain Organogenesis Program, Stanford, USA (GRID:grid.168010.e) (ISNI:0000000419368956) 
Pages
484-491
Publication year
2019
Publication date
Mar 2019
Publisher
Nature Publishing Group
ISSN
10976256
e-ISSN
15461726
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2185064360
Copyright
2019© The Author(s), under exclusive licence to Springer Nature America, Inc. 2019