细胞分裂角度调节组织机制,调整小脑折叠的数量
Amber G Cook1, Taylor V Bishop1, Hannah R Crowe1
1Mississippi State University, United States.
bioRxiv : the preprint server for biology
|July 28, 2023
概括
神经组织折叠,就像小脑一样,由差异扩张和层厚度来调节. 在外部颗粒层 (EGL) 中的细胞分裂角度调整这些因素以控制折叠量和波长.
科学领域:
- 发育生物学是发展生物学.
- 神经科学是一个神经科学.
- 生物物理学的生物物理.
背景情况:
- 神经组织折叠,特别是在小脑,是一个由机械力量影响的复杂过程.
- 以前的建模研究表明,组织层之间的差异扩张和外层厚度分别决定了折叠量和波长.
研究的目的:
- 研究神经组织折叠的拟议机制,使用具有不同小脑折叠的遗传特异性小鼠菌株.
- 确定关键的发育时期和调节大脑小脑折叠量和波长的细胞机制.
主要方法:
- 使用了表现出明显大脑小脑折叠模式的内生小鼠菌株.
- 在关键发育时期,分析了外部颗粒层 (EGL) 和小脑核之间的差异扩张的区域变化.
- 测量了EGL厚度,并将其与折叠波长相关联.
- 研究了SHH表达的Purkinje细胞和EGL增殖率.
- 检查了EGL内部的细胞分裂角度及其与触角扩张和EGL厚度的关系.
主要成果:
- 确定了一个关键时期,在此期间,小脑折叠量在小鼠菌株之间有所不同.
- 在EGL和小脑核之间的区域差异扩张与折叠量相关.
- 在此期间,EGL厚度在区域调整,与折叠波长的变化相关.
- 虽然SHH表达的Purkinje细胞数量预测了折叠数量,但EGL增殖率在各种菌株中是相似的.
- 在EGL细胞分裂角度的区域变化预测了接触式扩张和EGL厚度.
结论:
- 在EGL内部的细胞分裂角度作为一个可调的机制.
- 根据细胞分裂角度对差异扩张和EGL厚度的区域调整决定了小脑折叠量和波长.
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