Luo Xueying, Zhong Binlong, Hong Xian, Cui Yurong, Gao Ying, Yin Mengmeng, Tang Ming, Hescheler Jürgen, Xi Jiaoya
Cell Physiol Biochem. 2016;38(4):1333-42. doi: 10.1159/000443077. Epub 2016 Mar 24.
Puerarin, which shows beneficial and protective effects on cardiovascular diseases, is the main isoflavone extracted from Pueraria lobata (kudzu) root. The aim of this study was to investigate the effects of puerarin on in vitro myocardial proliferation and its underlying mechanism.
Myocardial differentiation of transgenic embryonic stem (ES) cells was performed by embryoid body-based differentiation method. The proliferation assay of cardiomyocytes (CMs) derived from ES cells (ES-CMs) was performed by EdU (5-Ethynyl-2'-deoxyuridine) staining. Flow cytometry was employed to determine the cell cycle distribution and apoptosis of purified ES-CMs. Quantitative real-time PCR was utilized to study the transcription of genes related to cell cycle progression. Signaling pathways relating to proliferation were studied by western blot analysis and application of specific inhibitors.
Puerarin exerted a delayed inhibitory effect on the proliferation of ES-CMs at the early-stage differentiation. Meanwhile, puerarin slowed progression through G2/M phase without inducing apoptosis of ES-CMs. Further assays showed that puerarin up-regulated the transcription of Cyclin A2, Cyclin B1 and Cdk1 in ES-CMs. The ERK1/2 specific inhibitor PD0325901 and the PI3K specific inhibitor Wortmannin successfully reversed puerarin-induced up-regulation of Cdk1 but not Cyclin A2 and B1.
These findings suggest that puerarin inhibits CM proliferation via slowing progression through G2/M phase during early-stage differentiation.
葛根素是从葛根中提取的主要异黄酮,对心血管疾病具有有益和保护作用。本研究旨在探讨葛根素对体外心肌增殖的影响及其潜在机制。
采用基于胚状体的分化方法对转基因胚胎干细胞(ES细胞)进行心肌分化。通过EdU(5-乙炔基-2'-脱氧尿苷)染色对ES细胞来源的心肌细胞(ES-CMs)进行增殖检测。运用流式细胞术测定纯化的ES-CMs的细胞周期分布和凋亡情况。利用定量实时PCR研究与细胞周期进程相关基因的转录。通过蛋白质印迹分析和应用特异性抑制剂研究与增殖相关的信号通路。
葛根素在早期分化阶段对ES-CMs的增殖具有延迟抑制作用。同时,葛根素减缓了ES-CMs通过G2/M期的进程,且未诱导其凋亡。进一步检测表明,葛根素上调了ES-CMs中细胞周期蛋白A2、细胞周期蛋白B1和细胞周期蛋白依赖性激酶1(Cdk1)的转录。ERK1/2特异性抑制剂PD0325901和PI3K特异性抑制剂渥曼青霉素成功逆转了葛根素诱导的Cdk1上调,但未逆转细胞周期蛋白A2和B1的上调。
这些发现表明,葛根素通过在早期分化阶段减缓ES-CMs通过G2/M期的进程来抑制心肌细胞增殖。