代谢,细胞表面组织,以及疾病
James W Dennis1, Ivan R Nabi, Michael Demetriou
1Samuel Lunenfeld Research Institute, Mount Sinai Hospital, Toronto, Ontario M5G 1X5, Canada. dennis@mshri.on.ca
Cell
|January 13, 2010
概括
代谢物可用性控制细胞表面的宏分子组合,影响信号传递和基因表达. 这一过程涉及N-糖化,影响了诸如衰老和代谢综合征等疾病.
科学领域:
- 分子生物学分子生物学
- 细胞生物学 细胞生物学
- 生物化学 生物化学
背景情况:
- 遗传信息流 (DNA到蛋白质) 传统上主导着分子组织.
- 新出现的证据强调了代谢物可用性作为一个关键的调节者.
- 对于这种调节,赫索胺和N-糖基化途径至关重要.
研究的目的:
- 调查代谢物可用性在宏分子复合组合中的作用.
- 了解N-糖化如何影响细胞表面糖蛋白的分布.
- 探索糖化缺陷与慢性疾病之间的联系.
主要方法:
- 对赫索胺和戈尔吉N-甘化途径的分析.
- 研究代谢物可用性对宏分子复合组件的影响.
- 调查N-甘氨酸结构和数量对莱克结合的影响.
主要成果:
- 代谢物的可用性到N-糖基化途径控制细胞表面复合组合.
- 这种控制作用于信号传递和基因表达的上游.
- N-甘氨酸的结构和数量通过莱克结合来调节糖蛋白的分布.
结论:
- 代谢物控制的N-糖化是细胞组织的一个基本机制.
- 糖化中的缺陷,从严重的障碍到轻微的缺陷,都与慢性疾病有关.
- 了解这些途径可以了解衰老,自身免疫和代谢综合征.
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