类有机物
生物
细胞结构
细胞命运测定
转录组
神经科学
发育生物学
细胞生物学
计算生物学
进化生物学
遗传学
转录因子
基因表达
基因
作者
Ilaria Chiaradia,Iván Imaz-Rosshandler,Benedikt S. Nilges,Jérôme Boulanger,Laura Pellegrini,Richa Das,Nachiket D. Kashikar,Madeline A. Lancaster
出处
期刊:Cell Stem Cell
[Elsevier]
日期:2023-10-01
卷期号:30 (10): 1351-1367.e10
被引量:19
标识
DOI:10.1016/j.stem.2023.09.003
摘要
Progression through fate decisions determines cellular composition and tissue architecture, but how that same architecture may impact cell fate is less clear. We took advantage of organoids as a tractable model to interrogate this interaction of form and fate. Screening methodological variations revealed that common protocol adjustments impacted various aspects of morphology, from macrostructure to tissue architecture. We examined the impact of morphological perturbations on cell fate through integrated single nuclear RNA sequencing (snRNA-seq) and spatial transcriptomics. Regardless of the specific protocol, organoids with more complex morphology better mimicked in vivo human fetal brain development. Organoids with perturbed tissue architecture displayed aberrant temporal progression, with cells being intermingled in both space and time. Finally, encapsulation to impart a simplified morphology led to disrupted tissue cytoarchitecture and a similar abnormal maturational timing. These data demonstrate that cells of the developing brain require proper spatial coordinates to undergo correct temporal progression.
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