Key Laboratory of Arrhythmias of the Ministry of Education of China Research Center for Translational Medicine Shanghai East Hospital Tongji University School of Medicine Shanghai China.
Department of Cardiology Shanghai East Hospital Tongji University School of Medicine Shanghai China.
J Am Heart Assoc. 2022 Aug 2;11(15):e026378. doi: 10.1161/JAHA.122.026378. Epub 2022 Jul 29.
Background The endothelium is essential for maintaining vascular physiological homeostasis and the endothelial injury leads to the neointimal hyperplasia because of the excessive proliferation of vascular smooth muscle cells. Endothelial Foxp1 (forkhead box P1) has been shown to control endothelial cell (EC) proliferation and migration in vitro. However, whether EC-Foxp1 participates in neointimal formation in vivo is not clear. Our study aimed to investigate the roles and mechanisms of EC-Foxp1 in neointimal hyperplasia. Methods and Results The wire injury femoral artery neointimal hyperplasia model was performed in Foxp1 EC-specific loss-of-function and gain-of-function mice. EC-Foxp1 deletion mice displayed the increased neointimal formation through elevation of vascular smooth muscle cell proliferation and migration, and the reduction of EC proliferation hence reendothelialization after injury. In contrast, EC-Foxp1 overexpression inhibited the neointimal formation. EC-Foxp1 paracrine regulated vascular smooth muscle cell proliferation and migration via targeting matrix metalloproteinase-9. Also, EC-Foxp1 deletion impaired EC repair through reduction of EC proliferation via increasing cyclin dependent kinase inhibitor 1B expression. Delivery of cyclin dependent kinase inhibitor 1B-siRNA to ECs using RGD (Arg-Gly-Asp)-peptide magnetic nanoparticle normalized the EC-Foxp1 deletion-mediated impaired EC repair and attenuated the neointimal formation. EC-Foxp1 regulates matrix metalloproteinase-9/cyclin dependent kinase inhibitor 1B signaling pathway to control injury induced neointimal formation. Conclusions Our study reveals that targeting EC-Foxp1-matrix metalloproteinase-9/cyclin dependent kinase inhibitor 1B pathway might provide future novel therapeutic interventions for restenosis.
内皮细胞对于维持血管生理稳态至关重要,内皮损伤会导致血管平滑肌细胞过度增殖,从而引起新生内膜增生。体外研究表明,叉头框蛋白 P1(Foxp1)可控制内皮细胞(EC)的增殖和迁移。然而,EC-Foxp1 是否参与体内新生内膜形成尚不清楚。本研究旨在探讨 EC-Foxp1 在新生内膜增生中的作用和机制。
在 Foxp1 内皮细胞特异性功能丧失和功能获得的小鼠中进行了线损伤股动脉新生内膜增生模型实验。EC-Foxp1 缺失小鼠通过增加血管平滑肌细胞增殖和迁移,降低内皮细胞增殖和损伤后再内皮化,导致新生内膜形成增加。相反,EC-Foxp1 过表达抑制了新生内膜形成。EC-Foxp1 旁分泌通过靶向基质金属蛋白酶-9 调节血管平滑肌细胞增殖和迁移。此外,EC-Foxp1 缺失通过增加周期蛋白依赖性激酶抑制剂 1B 的表达减少内皮细胞增殖,从而损害内皮修复。使用 RGD(精氨酸-甘氨酸-天冬氨酸)-肽磁纳米颗粒将周期蛋白依赖性激酶抑制剂 1B-siRNA 递送至 ECs,可使 EC-Foxp1 缺失介导的内皮修复受损正常化,并减弱新生内膜形成。
EC-Foxp1 调节基质金属蛋白酶-9/周期蛋白依赖性激酶抑制剂 1B 信号通路,控制损伤诱导的新生内膜形成。
本研究揭示了靶向 EC-Foxp1-基质金属蛋白酶-9/周期蛋白依赖性激酶抑制剂 1B 通路可能为再狭窄提供未来新的治疗干预措施。