SPI1抑制了血管内皮细胞中的YAP酸化,以防止内动脉瘤的进展
Yikui Liu1, Danyi Zheng2, Lanlan Zhao3
1Department of Neurosurgery, Ruijin Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Neurochemistry international
|December 11, 2025
概括
在内动脉瘤 (IAs) 中的流减少了YAP的表达,促进了内皮细胞衰老. SPI1过度表达可以抵消这种作用,为IA治疗提供了潜在的治疗点.
科学领域:
- 血管生物学 血管生物学
- 细胞机制 细胞机制
- 动脉瘤病变的发生因子
背景情况:
- 内动脉瘤 (IAs) 涉及复杂的内皮细胞 (EC) 功能障碍.
- 在IA开发的背景下,YAP在ECs中的作用尚未完全被理解.
研究的目的:
- 调查YAP在IA形成期间调解EC活动的机制.
- 确定非侵入性IA治疗的新型治疗点.
主要方法:
- 动脉瘤细胞的单核RNA测序.
- 人体IA组织和动脉壁的免疫染.
- 在人类大脑微血管内皮细胞 (HBMECs) 中YAP的淘汰.
- SPI1 (PU.1) 过度表达的研究.
主要成果:
- 在IA中EC显示中间的动脉/静脉/毛细血管身份.
- 流降低了YAP的调节,并在EC中增加了化YAP (p-YAP).
- 在HBMEC中YAP的淘汰会增加衰老标志物 (p21,p16) 并减少扩散/迁移.
- 通过YAP酸化抑制,SPI1过度表达减轻了由流引起的EC退化.
结论:
- 流通过减少YAP表达和增加其酸化来加速内皮老化.
- SPI1过度表达是一种潜在的治疗策略,通过减轻EC衰老来预防IA的进展.
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