摘要
目的 研究木犀草素对人主动脉平滑肌细胞迁移的调控作用,并探讨其调控作用是否通过激活内质网应激途径实现。方法 体外培养人主动脉平滑肌细胞,分为空白对照组(不做任何处理,BC)、阴性对照组(加等量无关试剂,NC)、木犀草素组(25μmol/L处理)、木犀草素+4-苯基丁酸钠共处理组(4-苯基丁酸钠预处理后加入等量木犀草素),于12h小时后细胞划痕实验法检测人主动脉平滑肌细胞迁移情况,Western blot和RTqPCR检测BIP、CHOP蛋白及RNA表达水平。结果 (1)与空白对照组和阴性对照组相比,木犀草素组细胞迁移水平明显降低,BIP、CHOP表达水平明显增高;(2)与木犀草素组相比,木犀草素+4-苯基丁酸钠共处理组细胞迁移水平增强,同时BIP、CHOP表达水平降低。结论 木犀草素通过上调内质网应激抑制人主动脉平滑肌细胞的迁移。
Objective To investigate the regulatory effect and mechanism of luteolin on the migration of human aortic smooth muscle cells(HASMCs).Methods HASMCs were cultured in vitro and divided into the blank control group(without any treatment,BC),the negative control group(with the same amount of irrelevant reagent,NC),the luteolin group(25 μmol/L treatment,LUT) and the luteolin+4-PBA treatment group(with the same amout of luteolin added after 4-PBA pretreatment,4-PBA).Cell scratch test was used to detect the HASMCs migration after 12hs.The expression level of BIP and CHOP about endoplasmic reticulum stress were detected by RTq PCR and Western blot.Results (1) Compared to the BC and NC groups,the cell migration level in the LUT group was significantly reduced,and the expression levels of BIP and CHOP were significantly increased.(2) Compared with the LUT group,the cell migration level of the luteolin+4-PBA co-teatment group increased,while the expression levels of BIP and CHOP decreased.Conclusion Luteolin inhibits HASMCs migration by promoting the endoplasmic reticulum stress.
作者
张黎
王清岑
周罗慧
杨娟
王红
Li ZHANG;Qingcen WANG;Luohui ZHOU;Juan YANG;Hong WANG(Ward Seventeen of Cardiovascular Medicine,The Affiliated Cardiovascular Hospital of Kunming Medical University,Kunming Yunnan 650500;Dept.of Cardiology,Panzhihua Integrated Traditional Chinese and Western Medicine Hospital,Panzhihua Sichuan 617000,China)
出处
《昆明医科大学学报》
CAS
2022年第5期12-17,共6页
Journal of Kunming Medical University
基金
云南省科技厅-昆明医科大学应用基础研究联合专项基金资助项目[2019FE001(-280)],云南省阜外心血管病医院心力衰竭诊疗省创新团队基金资助项目[201905E160013]。
关键词
木犀草素
内质网应激
人主动脉平滑肌细胞
迁移
Luteolin
Endoplasmic Reticulum stress
Human aortic smooth muscle cells
Migration