TRPV4型
兴奋剂
瞬时受体电位通道
血管生成
敌手
治疗性血管生成
血管
离子通道
药理学
TRPC1型
电压依赖性钙通道
血管舒张
血流
细胞生物学
化学
内分泌学
医学
钙
G蛋白偶联受体
血管平滑肌
硝苯地平
内科学
内皮
新生血管
癌症研究
受体拮抗剂
炎症
血管内皮生长因子
微血管
动脉发生
信号转导
TRPV公司
受体
作者
Gabriel Malka,Vanessa Salucci,Andreas Bergdahl
标识
DOI:10.1139/cjpp-2024-0383
摘要
Angiogenesis, the formation of new blood vessels, is crucial in ischemic heart disease to improve blood supply to the heart. Meanwhile, in cancer, inhibiting angiogenesis can limit tumor growth by reducing oxygen and nutrients. Calcium ions, key in cellular functions like proliferation and migration, play an important role in this process. Transient Receptor Potential Cation Channel, Vanilloid Subfamily Member 4 (TRPV4), a calcium-permeable channel, is highly expressed in endothelial cells lining blood vessels. This study explored the connection between TRPV4 and angiogenesis using an aortic ring assay. Aortic rings from 3-day-old C57Bl/6 pups were exposed to TRPV4 agonist (GSK1016790) and antagonist (HC067047) and standard growth media (control) after which maximal length and number of new sprouts were measured. The study found that the antagonist significantly reduced the number and length of new micro vessels, while the agonist increased sprout length. These findings highlight TRPV4's role in vascular remodeling, suggesting it could be a therapeutic target for treating diseases related to impaired blood flow and abnormal angiogenesis.
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