细胞死亡和控制细胞存活在寡头细胞谱系中的细胞死亡和控制
B A Barres1, I K Hart, H S Coles
1Medical Research Council Developmental Neurobiology Programme, University College, London, England.
Cell
|July 10, 1992
概括
发育中的动物的正常细胞死亡,如老鼠视神经中的寡细胞,通常是由于生存因素的竞争. 增加血小板衍生生长因子显著减少细胞死亡和增加细胞数量.
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
- 细胞生物学 细胞生物学
背景情况:
- 正常细胞死亡在发育中的动物组织中很普遍,但其原因在很大程度上仍然未知.
- 氧基细胞是中枢神经系统中关键的质细胞,负责髓膜的形成.
研究的目的:
- 为了研究在成长中的老鼠视神经中正常的寡类细胞死亡的原因.
- 为了确定涉及到寡头细胞发育和存活的特定生存因素.
主要方法:
- 在发育中的老鼠视神经中量化寡细胞死亡.
- 评估血小板衍生生长因子 (PDGF) 和胰岛素类生长因子 (IGFs) 对体内寡细胞存活率的影响.
- 在体内操纵PDGF水平,观察对寡细胞数量和死亡率的影响.
主要成果:
- 大约50%的寡细胞通常会在成长中的老鼠视神经中经历细胞死亡.
- 血小板衍生生长因子和类似胰岛素的生长因子作为寡细胞及其前体的生存因子.
- 在正在发育的视神经中增加PDGF水平,可将寡头细胞死亡率降低高达90%,并在4天内使寡头细胞数量翻一番.
结论:
- 在成长中的老鼠视神经中,正常的寡细胞死亡主要是由对有限的生存信号的竞争驱动的.
- 生存因子,如PDGF,在发育过程中在调节寡细胞数量方面发挥着关键作用.
- 对生存因素的竞争原则可以扩展到非神经组织中的正常细胞死亡.
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