TY - JOUR
T1 - Human fetal brain self-organizes into long-term expanding organoids
AU - Hendriks, Delilah
AU - Pagliaro, Anna
AU - Andreatta, Francesco
AU - Ma, Ziliang
AU - van Giessen, Joey
AU - Massalini, Simone
AU - López-Iglesias, Carmen
AU - van Son, Gijs J F
AU - DeMartino, Jeff
AU - Damen, J Mirjam A
AU - Zoutendijk, Iris
AU - Staliarova, Nadzeya
AU - Bredenoord, Annelien L
AU - Holstege, Frank C P
AU - Peters, Peter J
AU - Margaritis, Thanasis
AU - Chuva de Sousa Lopes, Susana
AU - Wu, Wei
AU - Clevers, Hans
AU - Artegiani, Benedetta
N1 - Copyright © 2023 The Author(s). Published by Elsevier Inc. All rights reserved.
PY - 2024/1
Y1 - 2024/1
N2 - 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.
AB - 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.
KW - Brain/cytology
KW - Central Nervous System/metabolism
KW - Extracellular Matrix/metabolism
KW - Humans
KW - Morphogenesis
KW - Organoids
KW - Pluripotent Stem Cells/metabolism
KW - Prosencephalon/cytology
KW - Stem Cells/metabolism
KW - Tissue Culture Techniques
KW - CRISPR-Cas9
KW - ECM
KW - brain cancer
KW - brain development
KW - human fetal brain
KW - morphogens
KW - organoids
KW - regional identity
KW - tissue culture
KW - tumor modeling
UR - https://www.mendeley.com/catalogue/fd8d3ab9-17d0-36a8-9e03-0835f14795a7/
U2 - 10.1016/j.cell.2023.12.012
DO - 10.1016/j.cell.2023.12.012
M3 - Article
C2 - 38194967
SN - 0092-8674
VL - 187
SP - 712-732.e38
JO - Cell
JF - Cell
IS - 3
ER -