4.8 Article

Self-organized developmental patterning and differentiation in cerebral organoids

期刊

EMBO JOURNAL
卷 36, 期 10, 页码 1316-1329

出版社

WILEY
DOI: 10.15252/embj.201694700

关键词

development; human brain development; neurogenesis; organoid; patterning; signaling

资金

  1. Marie Curie Postdoctoral Fellowship
  2. Medical Research Council [MC_UP_1201/9]
  3. Austrian Academy of Sciences
  4. Austrian Science Fund [I_1281-B19, Z_153_B09]
  5. European Research Council (ERC)
  6. Burroughs Wellcome Fund Career Awards at the Scientific Interface
  7. Searle Scholars Program
  8. Packard award in Science and Engineering
  9. NARSAD Young Investigator Award
  10. JPB Foundation (PIIF)
  11. JPB Foundation (PNDRF)
  12. NCSOFT Cultural Foundation
  13. NIH [1-U01-NS090473-01]
  14. Austrian Science Fund (FWF) [Z153] Funding Source: Austrian Science Fund (FWF)
  15. Austrian Science Fund (FWF) [Z 153] Funding Source: researchfish
  16. Medical Research Council [MC_UP_1201/9] Funding Source: researchfish
  17. MRC [MC_UP_1201/9] Funding Source: UKRI

向作者/读者索取更多资源

Cerebral organoids recapitulate human brain development at a considerable level of detail, even in the absence of externally added signaling factors. The patterning events driving this self-organization are currently unknown. Here, we examine the developmental and differentiative capacity of cerebral organoids. Focusing on forebrain regions, we demonstrate the presence of a variety of discrete ventral and dorsal regions. Clearing and subsequent 3D reconstruction of entire organoids reveal that many of these regions are interconnected, suggesting that the entire range of dorso-ventral identities can be generated within continuous neuroepithelia. Consistent with this, we demonstrate the presence of forebrain organizing centers that express secreted growth factors, which may be involved in dorso-ventral patterning within organoids. Furthermore, we demonstrate the timed generation of neurons with mature morphologies, as well as the subsequent generation of astrocytes and oligodendrocytes. Our work provides the methodology and quality criteria for phenotypic analysis of brain organoids and shows that the spatial and temporal patterning events governing human brain development can be recapitulated in vitro.

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