晚期视网膜原始体中Meis因子的过度表达会对时间模式和神经发生产生复杂的影响
bioRxiv : the preprint server for biology
|July 14, 2025
概括
在视网膜原生细胞 (RPC) 中过度表达Meis1和Meis2并没有诱导早期细胞类型. Meis1减少了增殖,而Meis2加速了神经发生,在没有完全重编程的情况下影响时间认同.
科学领域:
- 神经科学是一个神经科学.
- 发展生物学 发展生物学
- 眼科医生 眼科 眼科
背景情况:
- 脊椎动物视网膜是神经发生和细胞命运规范的关键模型.
- 视网膜原生细胞 (RPC) 通过精确的时间序列产生多种细胞类型.
- 转录因子Meis1和Meis2在晚期RPC中的作用尚不清楚.
研究的目的:
- 调查在产后小鼠RPC中过度表达Meis1和Meis2是否可以改变它们的时间身份.
- 确定Meis1和Meis2的过度表达是否可以在晚期RPC中诱导早产的视网膜细胞类型.
主要方法:
- 使用电穿孔将Meis1和Meis2输送到产后小鼠RPC中.
- 采用单细胞RNA测序来分析转录变化.
- 对增殖,神经发生和细胞命运承诺的评估影响.
主要成果:
- 梅斯1和梅斯2适度上调早期基因调节网络组件.
- 两者都没有抑制晚期转录因子,也没有诱导早产的视网膜细胞.
- Meis1的过度表达抑制了增殖和神经发生;Meis2加速了神经性进展,但没有改变命运的承诺.
结论:
- 在RPC中,Meis1和Meis2影响时间认同和神经性能力的不同方面.
- 这些因素的过度表达不足以完全重编程晚期视网膜前代.
- 这些发现为涉及视网膜细胞重编程的治疗策略提供了洞察力.
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