类有机物
生物
神经科学
诱导多能干细胞
细胞生物学
祖细胞
祖细胞
细胞外基质
人脑
干细胞
胚胎干细胞
遗传学
基因
作者
Delilah Hendriks,Anna Pagliaro,Francesco Andreatta,Ziliang Ma,Joey van Giessen,Simone Massalini,Carmen López‐Iglesias,Gijs J.F. van Son,Jeff DeMartino,J Damen,Iris Zoutendijk,Nadzeya Staliarova,Annelien L. Bredenoord,Frank C. P. Holstege,Peter J. Peters,Thanasis Margaritis,Susana M. Chuva de Sousa Lopes,Wei Wu,Hans Clevers,Benedetta Artegiani
出处
期刊:Cell
[Elsevier]
日期:2024-01-08
卷期号:187 (3): 712-732.e38
被引量:18
标识
DOI:10.1016/j.cell.2023.12.012
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI