小窝蛋白1
细胞外
细胞生物学
钙化
表皮生长因子
表皮生长因子受体
内科学
医学
生物发生
胞外囊泡
生长因子
小泡
小窝
化学
生物
癌症研究
受体
微泡
信号转导
生物化学
膜
基因
小RNA
作者
Amirala Bakhshian Nik,Hooi Hooi Ng,Sophie K. Ashbrook,Patrick Sun,Francesco Iacoviello,Paul R. Shearing,Sérgio Bertazzo,Deniel Mero,Bohdan B. Khomtchouk,Joshua D. Hutcheson
出处
期刊:American Journal of Physiology-heart and Circulatory Physiology
[American Physiological Society]
日期:2023-04-01
卷期号:324 (4): H553-H570
被引量:5
标识
DOI:10.1152/ajpheart.00280.2022
摘要
Here, we investigate the potential of epidermal growth factor receptor (EGFR) inhibition to prevent vascular calcification, a leading indicator of and contributor to cardiovascular morbidity and mortality. EGFR interacts and affects the trafficking of the plasma membrane scaffolding protein caveolin-1. Previous studies reported a key role for caveolin-1 in the development of specialized extracellular vesicles that mediate vascular calcification; however, no role of EGFR has been reported. We demonstrated that EGFR inhibition modulates caveolin-1 trafficking and hinders calcifying extracellular vesicle formation, which prevents vascular calcification. Given that EGFR inhibitors are clinically approved for other indications, this may represent a novel therapeutic strategy for vascular calcification.
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