钙化
细胞周期蛋白依赖激酶1
内皮干细胞
成骨细胞
细胞生物学
血管平滑肌
CDK抑制剂
化学
内科学
内分泌学
细胞周期蛋白依赖激酶
生物
癌症研究
医学
细胞周期
细胞
生物化学
体外
平滑肌
作者
Yan Zhao,Yang Yang,Xiuju Wu,Li Zhang,Xinjiang Cai,Jaden Ji,Sydney Chen,Abigail Vera,Kristina I. Boström,Yucheng Yao
出处
期刊:PubMed
[National Institutes of Health]
日期:2024-03-08
卷期号:9 (5)
被引量:5
标识
DOI:10.1172/jci.insight.176065
摘要
Vascular calcification is a severe complication of cardiovascular diseases. Previous studies demonstrated that endothelial lineage cells transitioned into osteoblast-like cells and contributed to vascular calcification. Here, we found that inhibition of cyclin-dependent kinase (CDK) prevented endothelial lineage cells from transitioning to osteoblast-like cells and reduced vascular calcification. We identified a robust induction of CDK1 in endothelial cells (ECs) in calcified arteries and showed that EC-specific gene deletion of CDK1 decreased the calcification. We found that limiting CDK1 induced E-twenty-six specific sequence variant 2 (ETV2), which was responsible for blocking endothelial lineage cells from undergoing osteoblast differentiation. We also found that inhibition of CDK1 reduced vascular calcification in a diabetic mouse model. Together, the results highlight the importance of CDK1 suppression and suggest CDK1 inhibition as a potential option for treating vascular calcification.
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