Xiang Min, Yang Runlin, Zhang Yaqin, Wu Pingping, Wang Lizhen, Gao Zhenyu, Wang Jianmei
Department of Pharmacy, Suzhou Health College, Suzhou, Jiangsu 215009, China.
Key Laboratory of Nuclear Medicine, Ministry of Health, Jiangsu Key Laboratory of Molecular Nuclear Medicine, Jiangsu Institute of Nuclear Medicine, Wuxi, Jiangsu 214063, China.
Microvasc Res. 2017 Jul;112:30-36. doi: 10.1016/j.mvr.2017.02.004. Epub 2017 Feb 13.
Crocetin is a major active constituent of Gardenia jasminoides J. Ellis, and can aid in the prevention of cardiovascular disease. The effect and possible mechanism of crocetin on the migration of vascular smooth muscle cells (VSMCs) induced by advanced glycosylation end products (AGEs) were investigated. VSMCs were pre-incubated with or without crocetin and exposed to AGEs subsequently. The invasion of the cells was investigated using a 24-well Cell Invasion Chamber. The anti-proliferative activity of crocetin was evaluated by MTT assay and VSMCs cell-cycle distribution was examined by flow cytometry. Cytokine TNF-α and IL-6 secreted by VSMCs and the amount of matrix metalloproteinase MMP-2 and MMP-9 in the culture supernatant were detected by ELISA. The expression level of RAGE (AGEs receptor), in cells was analyzed by western blot. The results demonstrated that AGEs increased about two-fold migration of VSMCs compared with control (OD=0.778±0.191 vs OD=0.413±0.214, P<0.01), and the proliferation increased by about 20% (OD=0.335±0.043 vs OD=0.281±0.037, P<0.01). Pre-treatment with crocetin (1.0μM) or RAGE antibody (10μg/ml) could inhibit the AGEs triggered migration of VSMCs obviously. Furthermore, both crocetin and RAGE antibody inhibited the increase of RAGE protein in VSMCs stimulated by AGEs. The levels of TNF-α and IL-6 decreased in the crocetin (1.0μM) pre-treated group compared to the AGEs (without pre-treated) group (37.60±3.08pg/ml vs 46.59±1.92pg/ml, 32.11±4.69pg/ml vs 49.99±8.84pg/ml, respectively). Crocetin (1.0μM) also reduced the value of MMP-2 and MMP-9 compared with the AGEs group (2.81±0.35ng/ml vs 6.40±0.85ng/ml, 2.69±0.25ng/ml vs 4.32±0.57ng/ml, respectively). In summary, crocetin inhibits the migration of VSMCs induced by AGEs through RAGE-dependent signaling pathway. And it is meaningful to diabetic vascular complications.
西红花酸是栀子的主要活性成分,有助于预防心血管疾病。研究了西红花酸对晚期糖基化终产物(AGEs)诱导的血管平滑肌细胞(VSMCs)迁移的影响及可能机制。将VSMCs在有或没有西红花酸的情况下预孵育,随后暴露于AGEs。使用24孔细胞侵袭小室研究细胞的侵袭情况。通过MTT法评估西红花酸的抗增殖活性,并通过流式细胞术检测VSMCs细胞周期分布。通过ELISA检测VSMCs分泌的细胞因子TNF-α和IL-6以及培养上清液中基质金属蛋白酶MMP-2和MMP-9的量。通过蛋白质印迹分析细胞中RAGE(AGEs受体)的表达水平。结果表明,与对照组相比,AGEs使VSMCs的迁移增加了约两倍(OD = 0.778±0.191对OD = 0.413±0.214,P<0.01),增殖增加了约20%(OD = 0.335±0.043对OD = 0.281±0.037,P<0.01)。用西红花酸(1.0μM)或RAGE抗体(10μg/ml)预处理可明显抑制AGEs触发的VSMCs迁移。此外,西红花酸和RAGE抗体均抑制AGEs刺激的VSMCs中RAGE蛋白的增加。与AGEs(未预处理)组相比,西红花酸(1.0μM)预处理组中TNF-α和IL-6的水平降低(分别为37.60±3.08pg/ml对46.59±1.92pg/ml,32.11±4.69pg/ml对49.99±8.84pg/ml)。与AGEs组相比,西红花酸(1.0μM)也降低了MMP-2和MMP-9的值(分别为2.81±0.35ng/ml对6.40±0.85ng/ml,2.69±0.25ng/ml对4.32±0.57ng/ml)。总之,西红花酸通过RAGE依赖性信号通路抑制AGEs诱导的VSMCs迁移。这对糖尿病血管并发症具有重要意义。