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FGF8 介导的基因调控影响人类脑类器官的区域特征。

FGF8-mediated gene regulation affects regional identity in human cerebral organoids.

机构信息

Univ. Côte d'Azur (UniCA), CNRS, Inserm, Institut de Biologie Valrose (iBV), Nice, France.

GenomEast platform, Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), Illkirch, France.

出版信息

Elife. 2024 Nov 1;13:e98096. doi: 10.7554/eLife.98096.

Abstract

The morphogen FGF8 establishes graded positional cues imparting regional cellular responses modulation of early target genes. The roles of FGF signaling and its effector genes remain poorly characterized in human experimental models mimicking early fetal telencephalic development. We used hiPSC-derived cerebral organoids as an platform to investigate the effect of FGF8 signaling on neural identity and differentiation. We found that FGF8 treatment increases cellular heterogeneity, leading to distinct telencephalic and mesencephalic-like domains that co-develop in multi-regional organoids. Within telencephalic regions, FGF8 affects the anteroposterior and dorsoventral identity of neural progenitors and the balance between GABAergic and glutamatergic neurons, thus impacting spontaneous neuronal network activity. Moreover, FGF8 efficiently modulates key regulators responsible for several human neurodevelopmental disorders. Overall, our results show that FGF8 signaling is directly involved in both regional patterning and cellular diversity in human cerebral organoids and in modulating genes associated with normal and pathological neural development.

摘要

成纤维细胞生长因子 8(FGF8)作为形态发生素,建立了赋予区域细胞反应以调节早期靶基因的梯度位置线索。在模拟早期胎儿端脑发育的人类实验模型中,FGF 信号及其效应基因的作用仍未得到很好的描述。我们使用 hiPSC 衍生的大脑类器官作为研究 FGF8 信号对神经身份和分化影响的平台。我们发现 FGF8 处理增加了细胞异质性,导致多区域类器官中独特的端脑和中脑样区域共同发育。在端脑区域,FGF8 影响神经祖细胞的前后和背腹身份以及 GABA 能和谷氨酸能神经元之间的平衡,从而影响自发的神经元网络活动。此外,FGF8 能够有效地调节几个与人类神经发育障碍相关的关键调节因子。总的来说,我们的结果表明,FGF8 信号直接参与人类大脑类器官的区域模式形成和细胞多样性,并调节与正常和病理性神经发育相关的基因。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/78f6/11581432/bac7472f8b4a/elife-98096-fig1.jpg

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