类有机物
神经外胚层
组织工程
胚状体
生物
细胞生物学
三维细胞培养
大脑皮层
解剖
神经科学
生物医学工程
胚胎干细胞
细胞
中胚层
成体干细胞
医学
生物化学
遗传学
基因
作者
Madeline A. Lancaster,Nina S. Corsini,Simone Wolfinger,E. Hilary Gustafson,Alexander William Phillips,Thomas R. Burkard,Tomoki Otani,Frederick J. Livesey,Juergen A. Knoblich
摘要
Engineering human brain organoids with floating scaffolds enhances the maturity and reproducibility of cortical tissue structure. Three-dimensional cell culture models have either relied on the self-organizing properties of mammalian cells1,2,3,4,5,6 or used bioengineered constructs to arrange cells in an organ-like configuration7,8. While self-organizing organoids excel at recapitulating early developmental events, bioengineered constructs reproducibly generate desired tissue architectures. Here, we combine these two approaches to reproducibly generate human forebrain tissue while maintaining its self-organizing capacity. We use poly(lactide-co-glycolide) copolymer (PLGA) fiber microfilaments as a floating scaffold to generate elongated embryoid bodies. Microfilament-engineered cerebral organoids (enCORs) display enhanced neuroectoderm formation and improved cortical development. Furthermore, reconstitution of the basement membrane leads to characteristic cortical tissue architecture, including formation of a polarized cortical plate and radial units. Thus, enCORs model the distinctive radial organization of the cerebral cortex and allow for the study of neuronal migration. Our data demonstrate that combining 3D cell culture with bioengineering can increase reproducibility and improve tissue architecture.
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