SOX2 and BRN2 as Key Transcription Factors in Neural Rosette Formation In Vitro

Zuzana Hudáčová
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Abstract

Although neurogenesis has been well studied, its molecular mechanisms remain largely unknown due to the challenges posed by the complexity of the underlying processes. Whilst in vivo studies can be used to study neurogenesis, the inability to control confounding variables complicate findings. Therefore, the purpose of this study was to identify the markers of in vitro neural rosette formation and describe the formation of neural rosettes from pluripotent stem cells using immunofluorescence analysis. The protocol of stem cell cultivation and induction of neural rosette formation was tested. Following, two transcription factors, BRN2 and SOX2, were fluorescently labelled and cells were imaged over a period of eight days. It was identified that SOX2 and BRN2 are expressed during in vitro neural rosette formation. These results are concurrent with in vivo neurogenesis, which suggests that neural rosettes could be a suitable in vitro model for researching neural development. Given that mistakes can arise during neurogenesis, such as neural tube defects, developing robust models to understand the formation of the nervous system is important. Moving forward, a detailed molecular understanding of neural rosette formation has the potential to be used for targeting specific transcription factors to treat or prevent problematic neurogenesis.
SOX2和BRN2是体外神经花环形成的关键转录因子
尽管神经发生已经得到了很好的研究,但由于潜在过程的复杂性所带来的挑战,其分子机制在很大程度上仍然未知。虽然体内研究可用于研究神经发生,但无法控制混杂变量使研究结果复杂化。因此,本研究的目的是鉴定体外神经莲座形成的标记物,并利用免疫荧光分析描述多能干细胞形成神经莲座的过程。试验了干细胞培养和诱导神经花环形成的方案。随后,对两种转录因子BRN2和SOX2进行荧光标记,并在8天内对细胞进行成像。SOX2和BRN2在体外神经花环形成过程中表达。这些结果与体内神经发生一致,表明神经玫瑰花可能是研究神经发育的合适体外模型。鉴于在神经发生过程中可能出现错误,例如神经管缺陷,开发健壮的模型来理解神经系统的形成是很重要的。展望未来,对神经花环形成的详细分子理解有可能用于靶向特定转录因子来治疗或预防有问题的神经发生。
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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