内分泌素标记和控制一个克拉素独立的内分泌细胞通路
Emmanuel Boucrot1, Antonio P A Ferreira2, Leonardo Almeida-Souza3
11] MRC Laboratory of Molecular Biology, Francis Crick Avenue, Cambridge CB2 0QH, UK [2] Institute of Structural and Molecular Biology, University College London &Birkbeck College, London WC1E 6BT, UK.
Nature
|December 18, 2014
概括
已经确定了一种新的内细胞路径,即快速内啡林介导内细胞分裂 (FEME). 这种不依赖于克拉的途径利用内啡来内化各种受体,特别是在细胞前端.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 内细胞分裂对于细胞过程至关重要,包括营养吸收和膜循环.
- 内分泌素传统上与克拉林介导的内分泌细胞形成有关.
- 一个独特的内细胞通路由内素调解尚未完全表征.
研究的目的:
- 识别和描述一种涉及内蛋白的新型内细胞路径.
- 为了阐明这个途径的分子机制和货物特异性.
- 调查内啡林在受体内化中的作用.
主要方法:
- 哺乳动物细胞培养和活细胞成像.
- 药理上抑制关键信号分子和细胞过程 (dynamin,Rac,PI3K,PAK1,actin聚合,Cdc42) 的作用.
- 在连接体刺激后对受体内部化的分析.
主要成果:
- 内啡林调解了一个快速的,管状细胞内细胞通路,独立于克拉斯林和AP2.
- 这一途径通过对各种G蛋白结合受体和受体氨酸激酶的连接体结合来激活.
- 该途径由脂氨醇-3,4-双酸盐,拉梅利波丁和特定的信号抑制剂调节.
结论:
- 快速内啡林介导内细胞分裂 (FEME) 是一个明显的克拉林独立的内细胞路径.
- FEME在许多重要的细胞表面受体的吸收中发挥着重要作用.
- 内分泌素是这种新型内细胞通路的关键调节剂,特别是在细胞的前沿.
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