4.8 Article

Guided self-organization and cortical plate formation in human brain organoids

期刊

NATURE BIOTECHNOLOGY
卷 35, 期 7, 页码 659-+

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NATURE PUBLISHING GROUP
DOI: 10.1038/nbt.3906

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资金

  1. Cambridge Wellcome Trust PhD program
  2. Marie Curie Postdoctoral fellowship
  3. Medical Research Council [MC_UP_1201/9]
  4. EMBO long-term fellowship
  5. Deutsche Forschungsgemeinschaft [DFG CO 1324/1-1]
  6. Austrian Academy of Sciences
  7. Austrian Science Fund [I_1281-B19, Z_153_B09]
  8. European Research Council
  9. MRC [MC_UP_1201/9, MR/L023784/2, MR/L023784/1] Funding Source: UKRI
  10. Medical Research Council [MC_UP_1201/9] Funding Source: researchfish

向作者/读者索取更多资源

Three-dimensional cell culture models have either relied on the self-organizing properties of mammalian cells(1-6) or used bioengineered constructs to arrange cells in an organ-like configuration(7,8). 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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