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Foxg1 拮抗新皮层干细胞向星形胶质细胞的分化。

Foxg1 Antagonizes Neocortical Stem Cell Progression to Astrogenesis.

机构信息

Laboratory of Cerebral Cortex Development, Neuroscience Area, SISSA, Trieste, Italy.

Department of Diagnostics, Institute for Maternal and Child Health, IRCCS Burlo Garofolo, Trieste, Italy.

出版信息

Cereb Cortex. 2019 Dec 17;29(12):4903-4918. doi: 10.1093/cercor/bhz031.

Abstract

Neocortical astrogenesis follows neuronogenesis and precedes oligogenesis. Among key factors dictating its temporal articulation, there are progression rates of pallial stem cells (SCs) towards astroglial lineages as well as activation rates of astrocyte differentiation programs in response to extrinsic gliogenic cues. In this study, we showed that high Foxg1 SC expression antagonizes astrocyte generation, while stimulating SC self-renewal and committing SCs to neuronogenesis. We found that mechanisms underlying this activity are mainly cell autonomous and highly pleiotropic. They include a concerted downregulation of 4 key effectors channeling neural SCs to astroglial fates, as well as defective activation of core molecular machineries implementing astroglial differentiation programs. Next, we found that SC Foxg1 levels specifically decline during the neuronogenic-to-gliogenic transition, pointing to a pivotal Foxg1 role in temporal modulation of astrogenesis. Finally, we showed that Foxg1 inhibits astrogenesis from human neocortical precursors, suggesting that this is an evolutionarily ancient trait.

摘要

新皮层神经发生先于少突胶质细胞发生,而后者又先于星形胶质细胞发生。在决定其时间表达的关键因素中,有神经上皮干细胞(SCs)向星形胶质细胞谱系的进展速度,以及对外源性神经胶质发生信号的反应中星形胶质细胞分化程序的激活速度。在这项研究中,我们表明高表达 Foxg1 的 SC 会拮抗星形胶质细胞的产生,同时刺激 SC 的自我更新并促使 SC 向神经元发生。我们发现,这种活性的机制主要是细胞自主的,而且具有高度的多效性。它们包括协调下调 4 个关键效应因子,将神经 SC 引导至星形胶质细胞命运,以及核心分子机制的缺陷激活,执行星形胶质细胞分化程序。接下来,我们发现 SC Foxg1 水平在神经元发生向神经胶质发生的转变过程中特异性下降,这表明 Foxg1 在星形胶质细胞发生的时间调节中起着关键作用。最后,我们发现 Foxg1 抑制了人类新皮层前体细胞的星形胶质细胞发生,这表明这是一个古老的特征。

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