4.8 Article

An in vivo model of functional and vascularized human brain organoids

期刊

NATURE BIOTECHNOLOGY
卷 36, 期 5, 页码 432-+

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nbt.4127

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资金

  1. Waitt Advanced Biophotonics Core
  2. Salk Stem Cell Core
  3. FACS Core
  4. Salk Institute
  5. NIH [U19 MH106434, U01 MH106882, R01NS083815, R01AG047669]
  6. Paul G, Allen Family Foundation
  7. The Leona M, and Harry B, Helmsley Charitable Trust [2012-PG-MED]
  8. The G, Harold and Leila Y, Mathers Foundation
  9. JPB Foundation
  10. Dolby Family Ventures
  11. CIRM Bridges to Stem Cell Research Internship Program
  12. EMBO Postdoctoral Longterm Fellowship [ALTF 1214-2014]
  13. EMBO Postdoctoral Longterm Fellowship (European Commission FP7-Marie Curie Actions, LTFCOFUND) [QGA-2013-609409]
  14. Human Frontiers Science Program (HFSP Long-Term Fellowship) [LT001074/2015]

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Differentiation of human pluripotent stem cells to small brain-like structures known as brain organoids offers an unprecedented opportunity to model human brain development and disease. To provide a vascularized and functional in vivo model of brain organoids, we established a method for transplanting human brain organoids into the adult mouse brain. Organoid grafts showed progressive neuronal differentiation and maturation, gliogenesis, integration of microglia, and growth of axons to multiple regions of the host brain. In vivo two-photon imaging demonstrated functional neuronal networks and blood vessels in the grafts. Finally, in vivo extracellular recording combined with optogenetics revealed intragraft neuronal activity and suggested graft-to-host functional synaptic connectivity. This combination of human neural organoids and an in vivo physiological environment in the animal brain may facilitate disease modeling under physiological conditions.

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