School of Pharmaceutical Science & Yunnan Key Laboratory of Pharmacology for Natural Products, Kunming Medical University, Kunming 650500, China ; Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
Department of Periodontology and Implant Dentistry, The First People's Hospital of Yun-Nan Province, Kunhua Hospital, Kunming University of Science and Technology, Kunming 650032, China.
Evid Based Complement Alternat Med. 2015;2015:278014. doi: 10.1155/2015/278014. Epub 2015 Oct 18.
Scutellarin (SCU) is one of the main components of traditional Chinese medicine plant Erigeron breviscapus (Vant.) Hand.-Mazz. In this paper, we studied the protective effects of SCU on human cardiac microvascular endothelial cells (HCMECs) against hypoxia-reoxygenation (HR) injury and its possible target-related proteins. Results of MTT assay showed that pretreatment of SCU at doses of 1, 5, and 10 μM for 2 h could significantly inhibit the decrease in cell viability of HCMECs induced by HR injury. Subcellular fractions of cells treated with vehicle control, 1 μM SCU, HR injury, or 1 μM SCU + HR injury were separated by ultracentrifugation. The protein expression profiles of cytoplasm and membrane/nuclei fractions were checked using protein two-dimensional electrophoresis (2-DE). Proteins differentially expressed between control and SCU-treated group, control and HR group, or HR and SCU + HR group were identified using mass spectrometry (MS/MS). Possible interaction network of these target-related proteins was predicted using bioinformatic analysis. The influence of SCU on the expression levels of these proteins was confirmed using Western blotting assay. The results indicated that proteins such as p27BBP protein (EIF6), heat shock 60 kDa protein 1 (HSPD1), and chaperonin containing TCP1 subunit 6A isoform (CCT6A) might play important roles in the effects of SCU.
野黄芩苷(SCU)是传统中药植物灯盏花(Vant.)Hand.-Mazz 的主要成分之一。在本文中,我们研究了 SCU 对人心脏微血管内皮细胞(HCMEC)对缺氧复氧(HR)损伤的保护作用及其可能的靶相关蛋白。MTT 检测结果表明,1、5 和 10 μM 的 SCU 预处理 2 h 可显著抑制 HR 损伤诱导的 HCMEC 活力下降。用载体对照、1 μM SCU、HR 损伤或 1 μM SCU+HR 损伤处理的细胞的亚细胞部分通过超速离心分离。使用蛋白质二维电泳(2-DE)检查细胞质和膜/核部分的蛋白质表达谱。使用质谱(MS/MS)鉴定对照和 SCU 处理组、对照和 HR 组或 HR 和 SCU+HR 组之间差异表达的蛋白质。使用生物信息学分析预测这些靶相关蛋白的可能相互作用网络。使用 Western blot 检测法证实了 SCU 对这些蛋白质表达水平的影响。结果表明,p27BBP 蛋白(EIF6)、热休克 60 kDa 蛋白 1(HSPD1)和包含 TCP1 亚基 6A 同工型的伴侣蛋白(CCT6A)等蛋白可能在 SCU 的作用中发挥重要作用。