自的丧失破坏了在衰老过程中芽细胞系细胞的干细胞
H Ida-Yonemochi1, K Otsu2, T Irié3
1Division of Anatomy and Cell Biology of the Hard Tissue, Department of Tissue Regeneration and Reconstruction, Niigata University Graduate School of Medical and Dental Sciences, Chuo-ku, Niigata, Japan.
Journal of dental research
|December 7, 2023
概括
自对于牙干细胞的维护和牙形成至关重要. 在小鼠中,它的缺乏导致细胞死亡,异常的切肢发育和潜在的瘤形成,特别是在压力和衰老下.
科学领域:
- 细胞生物学 细胞生物学
- 发育生物学 发展生物学
- 干细胞生物学 干细胞生物学
背景情况:
- 自是一种关键的细胞内降解途径,对细胞平衡至关重要.
- 它在牙上皮干细胞和牙形成中的作用在很大程度上仍未被探索.
- 了解自的功能对于口腔健康和疾病研究至关重要.
研究的目的:
- 调查自在维护牙上皮干细胞中的作用.
- 分析自性缺陷在衰老和压力期间对质形成的影响.
- 探索自功能障碍在诱导牙上皮细胞瘤发生方面的潜力.
主要方法:
- 在正常,老化和高血糖压力条件下对自缺陷小鼠 (Atg7f/f;KRT14-Cre) 的分析.
- 在体外细胞和器官培养实验中使用自抑制剂.
- 牙组织和细胞的形态学,组织学和分子分析.
主要成果:
- 自性缺陷导致年轻小鼠中介层中显著的细胞死亡.
- 过高血糖诱导了自性缺陷小鼠的切口的白色变色.
- 年龄较大的自性缺陷小鼠表现出不规则的顶角芽形态和牙瘤形成.
- 实验室培养物显示不典型的细胞扩大和表观遗传变化,表明瘤发生.
- 自抑制诱导了表观遗传变化和p21上调 in vivo 和 in vitro.
结论:
- 自对于调节牙上皮干细胞的维护,增殖和分化至关重要.
- 自性障碍与瘤发生有关的质上皮细胞瘤发生有关.
- 向自可能为牙发育障碍和口腔癌提供治疗策略.
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