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CDK1 inhibition reduces osteogenesis in endothelial cells in vascular calcification
Yan Zhao, … , Kristina I. Boström, Yucheng Yao
Yan Zhao, … , Kristina I. Boström, Yucheng Yao
Published January 23, 2024
Citation Information: JCI Insight. 2024;9(5):e176065. https://doi.org/10.1172/jci.insight.176065.
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Research Article Cell biology Vascular biology

CDK1 inhibition reduces osteogenesis in endothelial cells in vascular calcification

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Abstract

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.

Authors

Yan Zhao, Yang Yang, Xiuju Wu, Li Zhang, Xinjiang Cai, Jaden Ji, Sydney Chen, Abigail Vera, Kristina I. Boström, Yucheng Yao

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Figure 2

AT7519 prevents endothelial lineage cells from acquiring osteogenic capacity.

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AT7519 prevents endothelial lineage cells from acquiring osteogenic capa...
(A) Von Kossa staining and total calcium quantitation in osteogenesis assays using tdTomato+ aortic cells isolated from VE-cadherinCreERT2 RosatdTomato Mgp–/– mice treated with AT7519 (n = 9). VE-cadherinCreERT2 RosatdTomato mice were used as controls. Scale bars: 50 μm. (B) Tube formation assays using tdTomato+ aortic cells isolated from VE-cadherinCreERT2 RosatdTomato Mgp–/– mice treated with AT7519 (n = 9). VE-cadherinCreERT2 RosatdTomato mice were used as controls. Red, tdTomato. Scale bars: 50 μm. (C) Micro-CT images of ectopic bone formation with analysis of relative volume of bone formation and H&E staining after transplantation of tdTomato+ aortic cells isolated from VE-cadherinCreERT2 RosatdTomato Mgp–/– mice treated with AT7519 (n = 7). Saline was used as control. Scale bars: 5 mm (top) and 50 μm (bottom). (D) Laser Doppler perfusion images and immunostaining using anti-CD31 antibodies at ischemic sites after the transplantation of tdTomato+ aortic cells isolated from VE-cadherinCreERT2 RosatdTomato Mgp–/– mice treated with AT7519 (n = 8). Saline was used as control. Scale bars: 10 mm (top) and 50 μm (bottom). Data were analyzed for statistical significance by 1-way ANOVA with Tukey’s multiple-comparison test (A, B, and D) or unpaired, 2-tailed Student’s t test (C). In A–C, the bounds of the boxes are upper and lower quartiles with data points, the line in the box is the median, and whiskers are maximal and minimal values. Data in D are presented as mean ± SD. ***P < 0.0001.

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