Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA, USA.
Program in Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA, USA.
Nat Neurosci. 2019 Mar;22(3):484-491. doi: 10.1038/s41593-018-0316-9. Epub 2019 Jan 28.
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.
研究人类少突胶质细胞以及少突胶质细胞与神经元和星形胶质细胞的相互作用,将有助于我们理解脑白质疾病的发病机制。然而,由于功能性人脑组织的获取有限,这一研究极具挑战性。在此,我们开发了一种新的人类诱导多能干细胞分化方法,生成包含少突胶质细胞、神经元和星形胶质细胞的三维脑类器官,即人类少突胶质细胞球体。我们发现,人类少突胶质细胞球体中衍生的少突胶质细胞谱系细胞经历了类似于原代人类少突胶质细胞的发育阶段,并且可以通过活细胞成像来捕获少突胶质细胞谱系细胞的迁移及其对溶血卵磷脂暴露的敏感性。此外,它们的形态会随着在体外时间的延长而成熟并开始包裹神经元。我们预计,这种方法可用于研究少突胶质细胞的发育、髓鞘形成以及与中枢神经系统中其他主要细胞类型的相互作用。