Tissue morphology influences the temporal program of human brain organoid development.

Ilaria Chiaradia, Ivan Imaz-Rosshandler, Benedikt S Nilges, Jerome Boulanger, Laura Pellegrini, Richa Das, Nachiket D Kashikar, Madeline A Lancaster
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Abstract

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.

组织形态学影响人类大脑类器官发育的时间程序。
通过命运决定的进展决定了细胞组成和组织结构,但同样的结构如何影响细胞命运尚不清楚。我们利用类器官作为一个易于处理的模型来探究这种形式和命运的相互作用。筛选方法的变化表明,常见的方案调整影响了形态学的各个方面,从宏观结构到组织结构。我们通过整合单核RNA测序(snRNA-seq)和空间转录组学研究了形态扰动对细胞命运的影响。无论具体方案如何,形态更复杂的类器官都能更好地模拟体内人类胎儿大脑的发育。组织结构紊乱的类器官表现出异常的时间进展,细胞在空间和时间上都混杂在一起。最后,封装以赋予简化的形态导致组织细胞结构紊乱和类似的异常成熟时间。这些数据表明,发育中的大脑细胞需要适当的空间坐标才能进行正确的时间进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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