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作 者:朱丽华[1] 关红菁[1] 王朗[1] 田松[1] 杨妲[1] 付明月[1] 江洪[1]
出 处:《国际脑血管病杂志》2012年第3期189-192,共4页International Journal of Cerebrovascular Diseases
基 金:项目基金:国家自然科学基金青年科学基金(8100342);湖北省自然科学基金(2010CDB06203);武汉大学自主科研项目(3082017)
摘 要:目的探讨天麻素对血小板衍生生长因子一BB(platelet—derivedgrowthfactor—BB,PDGF—BB)诱导血管平滑肌细胞(vascularsmoothmusclecell,VSMC)迁移的影响及其可能机制。方法酶消化法获取大鼠主动脉VSMC并传代纯化。免疫荧光染色法对VSMC标记蛋白进行鉴定。建立PDGF—BB诱导细胞迁移模型。Transwell小室法评价天麻素对PDGF—BB诱导VSMC迁移的影响。蛋白质印迹法检测c—JunN末端激酶(c-junN—terminalkinase,JNK)磷酸化水平。结果原代培养的VSMC纯度达99%以上。PDGF—BB组VSMC迁移数量为(85.2±3.486)个觎野,显著多于对照组的(42.5±1.927)个/视野(t=9.981,P〈0.001),而天麻素能使PDGF—BB诱导VSMC迁移数量显著减少为(71.3±1.783)个觎野(t=3.550,P=0.002)。蛋白质印迹分析显示,天麻素能抑制PDGF—BB诱导的YNK磷酸化(0.190±0.015对0.190±0.015;t=14.548,P=0.000)。结论天麻素可抑制PDGF—BB诱导VSMC迁移,其机制可能与抑制JNK信号通路激活有关。Objective To investigate the effect of gastrodin on rat vascular smooth muscle cell (VSMC) migration induced by platelet-derived growth factor-BB (PDGF-BB) and its possible mechanisms. Methods Enzyme digestion method was used to obtain rat aortic VSMCs and be purified by passage. Immunofluorescence staining was used to identify VSMC marker proteins. A PDGF-BB induced cell migration model was established. Transwell chamber assay was used to evaluate the effect of gastrodin on PDGF-BB induced VSMC migration. Western blots were performed to detect the phosphorylation levels of c-jun N-termi- nal kinase (JNK). Results The purity of primary cultured VSMC was more than 99%. The VSMC migrated number in the PDGF-BB group was 85.2 ± 3. 486 per field. It was significantly more than 42. 5± 1. 927 per field in the control group (t=9. 981, P〈0. 001), and gastrodin was enable to make PDGF-BB induced the number of VSMC migration significantly reduce to 71.3 ±1. 783 per filed (t = 3. 550, P = 0. 002). Western blots analysis showed that gastrodin inhibited PDGF-BB induced JNK phosphorylation (0. 190 ± 0. 015 vs. 0. 190± 0. 015; t = 14. 548, P =0. 000). Conclusions Gastrodin inhibits PDGF-BB induced VSMC migration, its mechanisms may be associated with the inhibition of the JNK signaling pathway activation.
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