通过Src-TEM4-YAP通路对VEGF信号的动态解码和多种表型的协调控制
Sung Hoon Lee1, Tae-Yun Kang1, Xingbo Shang1
1Yale Systems Biology Institute, Yale University, West Haven, CT 06516, USA; Department of Biomedical Engineering, Yale University, New Haven, CT 06520, USA.
Cell systems
|June 20, 2025
概括
血管内皮生长因子 (VEGF) 通过一个连续的途径协调复杂的内皮细胞反应,如血管生成. 这一途径涉及Src,TEM4,YAP和Notch信号,使用反和振荡来控制随着时间的推移不同的细胞行为.
科学领域:
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
- 生理学 生理学 生理学
背景情况:
- 内皮细胞对血管内皮生长因子 (VEGF) 反应,细胞接触,重塑和血管生成发生变化,特别是在低氧条件下.
- 这些不同的VEGF驱动的细胞反应背后的协调和信号通路仍然不完全理解.
研究的目的:
- 阐明控制内皮细胞对VEGF反应的分子途径和信号动态.
- 了解细胞反应的不同时间尺度是如何通过VEGF信号协调的.
主要方法:
- 研究了信号分子的顺序激活,包括Src,瘤内皮标记物4 (TEM4),YAP和Notch信号组件.
- 分析了信号通路内的反调节和振荡的作用.
主要成果:
- 由VEGF诱导的内皮细胞反应通过一个顺序的途径得到控制:Src → TEM4 → YAP → Notch信号传递.
- 不同路径级别的反调节和振荡决定了功能结果.
- 更深层的路径层集成快速上游信号来控制较慢的表型变化.
结论:
- 已识别的途径为了解VEGF信号如何解码复杂的细胞反应提供了一个框架.
- 有着不同的时间尺度的途径组织确保了血管生成等重要生理过程的复杂性.
- 这种机制突显了内皮细胞生物学中复杂的信号处理.
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