A novel mechanism of inhibiting in-stent restenosis with arsenic trioxide drug-eluting stent: Enhancing contractile phenotype of vascular smooth muscle cells via YAP pathway
作者机构:Laboratory of Tissue and Cell BiologyLab Teaching&Management CenterChongqing Medical UniversityChongqing400016China Key Laboratory for Biorheological Science and Technology of Ministry of EducationState and Local Joint Engineering Laboratory for Vascular ImplantsBioengineering College of Chongqing UniversityChongqing400030China Beijing Amsinomed Medical Co.LtdBeijing100021China Medical SchoolNewcastle UniversityNewcastle Upon TyneNE24AXUK National Engineering Research Center for BiomaterialsSichuan UniversityChengdu610065China
出 版 物:《Bioactive Materials》 (生物活性材料(英文))
年 卷 期:2021年第6卷第2期
页 面:375-385页
核心收录:
学科分类:0831[工学-生物医学工程(可授工学、理学、医学学位)] 0710[理学-生物学] 08[工学] 0805[工学-材料科学与工程(可授工学、理学学位)] 0836[工学-生物工程]
基 金:This study was supported in part by grants from the National Natural Science Foundation of China,China(31971242,31701275) the National Science Foundation of Chongqing,China(cstc2020jcjymsxmX0189) the Chongqing Research Program of Basic Research and Frontier Technology,China(CSTC2019JCYJ-ZDXM0033) Open Fund for Key Laboratory of Biorheological Science and Technology,Ministry of Education,China(CQKLBST-2019-010) Innovation Talent Project of 2020 for Chongqing Primary and secondary School,China(CY200405) the National Key R&D Program,China(2016YFC1102305) The support from the Chongqing Engineering Laboratory in Vascular Implants,China,the Public Experiment Centre of State Bioindustrial Base(Chongqing)and the National“111 Plan”,China(B06023)are gratefully acknowledged
主 题:Arsenic trioxide(ATO) Bioactive Yes-associated protein(YAP) In-stent restenosis(ISR)
摘 要:Objective:Arsenic trioxide(ATO or As2O3)has beneficial effects on suppressing neointimal hyperplasia and restenosis,but the mechanism is still *** goal of this study is to further understand the mechanism of ATO s inhibitory effect on vascular smooth muscle cells(VSMCs).Methods and results:Through in vitro cell culture and in vivo stent implanting into the carotid arteries of rabbit,a synthetic-to-contractile phenotypic transition was induced and the proliferation of VSMCs was inhibited by ATO.F-actin filaments were clustered and the elasticity modulus was increased within the phenotypic modulation of VSMCs induced by ATO in ***,Yes-associated protein(YAP)nuclear translocation was inhibited by ATO both in vivo and in *** was found that ROCK inhibitor or YAP inactivator could partially mask the phenotype modulation of ATO on ***:The interaction of YAP with the ROCK pathway through ATO seems to mediate the contractile phenotype of *** provides an indication of the clinical therapeutic mechanism for the beneficial bioactive effect of ATO-drug eluting stent(AES)on in-stent restenosis(ISR).