Human fetal brain self-organizes into long-term expanding organoids

Delilah Hendriks, Anna Pagliaro, Francesco Andreatta, Ziliang Ma, Joey van Giessen, Simone Massalini, Carmen López-Iglesias, Gijs J F van Son, Jeff DeMartino, J Mirjam A Damen, Iris Zoutendijk, Nadzeya Staliarova, Annelien L Bredenoord, Frank C P Holstege, Peter J Peters, Thanasis Margaritis, Susana Chuva de Sousa Lopes, Wei Wu, Hans Clevers, Benedetta Artegiani

Onderzoeksoutput: Bijdrage aan tijdschriftArtikelpeer review

Samenvatting

Human brain development involves an orchestrated, massive neural progenitor expansion while a multi-cellular tissue architecture is established. Continuously expanding organoids can be grown directly from multiple somatic tissues, yet to date, brain organoids can solely be established from pluripotent stem cells. Here, we show that healthy human fetal brain in vitro self-organizes into organoids (FeBOs), phenocopying aspects of in vivo cellular heterogeneity and complex organization. FeBOs can be expanded over long time periods. FeBO growth requires maintenance of tissue integrity, which ensures production of a tissue-like extracellular matrix (ECM) niche, ultimately endowing FeBO expansion. FeBO lines derived from different areas of the central nervous system (CNS), including dorsal and ventral forebrain, preserve their regional identity and allow to probe aspects of positional identity. Using CRISPR-Cas9, we showcase the generation of syngeneic mutant FeBO lines for the study of brain cancer. Taken together, FeBOs constitute a complementary CNS organoid platform.

Originele taal-2Engels
Pagina's (van-tot)712-732.e38
TijdschriftCell
Volume187
Nummer van het tijdschrift3
Vroegere onlinedatum8 jan. 2024
DOI's
StatusGepubliceerd - jan. 2024

Trefwoorden

  • CRISPR-Cas9
  • ECM
  • brain cancer
  • brain development
  • human fetal brain
  • morphogens
  • organoids
  • regional identity
  • tissue culture
  • tumor modeling

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