粘附GPCR诱导的细胞外细胞分裂介导细胞间GPCR信号的传播
Guobing Huang1,2, Ni Li1,2, Yiyang Chen1,2
1Cellular Signaling Laboratory, Key Laboratory of Molecular Biophysics of Ministry of Education, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan, China.
Nature chemical biology
|February 13, 2026
概括
粘附G蛋白结合受体 (aGPCRs) 驱动新型细胞外囊泡 (EVs) 的形成,称为迁移体和回收体. 这些EV在细胞之间转移活跃的aGPCR,从而影响细胞通信和血管生成.
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:
- 细胞间的通信依赖于通过受体传输信号.
- 细胞外囊泡 (EVs) 是细胞间信号传递的关键媒介.
- G蛋白合受体 (GPCRs) 在EV介导通信中的作用基本上是未知的.
研究的目的:
- 调查GPCRs在EV介导细胞通信中的参与.
- 探索粘附GPCRs (aGPCRs) 在EV形成和信号传递中的功能.
主要方法:
- 研究了aGPCRs在迁移体和收缩体形成中的作用.
- 使用了G12/13蛋白信号通路.
- 检查了激活的aGPCRs的细胞外和细胞间转移.
- 在体外和体外评估了aGPCR转移对内皮细胞血管生成潜力的影响.
主要成果:
- aGPCRs通过其细胞外域和G12/13信号传递诱导迁移体和收缩体的形成.
- 被激活的aGPCRs通过细胞外释放到这些EV中,并被受体细胞内化.
- 癌症衍生的迁移体将aGPCRs (例如,GPR56) 转移到内皮细胞,增强血管生成.
结论:
- aGPCRs积极促进迁移体和收缩体的形成.
- 细胞间通信的一种新机制涉及活性GPCRs的EV介导的细胞间传播.
- 这一途径通过转移功能性的aGPCRs来促进癌症血管生成.
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