李婷婷 陈明云 李梅芳 陆俊茜 李连喜△.H3K9me3 参与调节高糖诱导大鼠胸主动脉平滑肌细胞增殖[J].现代生物医学进展英文版,2016,16(25):4801-4804. |
H3K9me3 参与调节高糖诱导大鼠胸主动脉平滑肌细胞增殖 |
H3K9me3 is involved in Proliferation of Rat Thoracic Aortic Smooth MuscleCells induced by High Glucose* |
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DOI: |
中文关键词: 组蛋白修饰 大鼠胸主动脉平滑肌A7r5 细胞 细胞增殖 p53 |
英文关键词: Histone modification Rat thoracic aortic muscle A7r5 cells Cell proliferation P53 |
基金项目:国家自然科学基金面上项目(81170759) |
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中文摘要: |
目的:研究H3K9me3 在高糖诱导大鼠胸主动脉平滑肌A7r5 细胞增殖中的作用,并初步探讨其可能的作用机制。方法:应用
MTT 法检测高糖刺激下不同浓度的H3K9 甲基转移酶SUV39H1 特异性抑制剂Chaetocin (0、10、25、50、75、100 nmol/L) 和50
nmol/LH3K9甲基转移酶SUV39H1特异性抑制剂Chaetocin在不同时间点(24、48、72 h和5 d) 对细胞增殖的影响。应用Western
bolt 法观察50 nmol/L H3K9甲基转移酶SUV39H1特异性抑制剂Chaetocin在高糖浓度下干预A7r5 细胞72 h 后,对H3K9me3
和p53 表达的影响。结果:Chaetocin 可显著抑制高糖诱导下A7r5 细胞的增殖,且抑制作用呈浓度和时间依赖性。与正常糖相比,
Chaetocin 可显著下调A7r5 细胞在高糖诱导下表达增多的H3K9me3,同时显著上调在高糖诱导下表达减少的p53(P<0.05)。结
论:高糖可通过H3K9me3 下调p53的表达促进大鼠胸主动脉平滑肌A7r5 细胞的增殖,H3K9 甲基转移酶SUV39H1 特异性抑制
剂Chaetocin 可抑制上述过程,为减少糖尿病大血管并发症提供了治疗的新思路。 |
英文摘要: |
Objective:To explore the effects of H3K9me3 on rat thoracic aortic smooth muscle A7r5 cell proliferation induced by
high glucose, and to study its underlying mechanism.Methods:Under the high glucose condition, MTT assays were applied to observe
the effects of different concentrations of H3K9 methyltransferase SUV39H1 specific inhibitor Chaetocin (0, 10, 25, 50, 75, 100 nmol/L)
and 50 nmol/L Chaetocin at different time points (24, 48, 72 h, 5 d)on rat thoracic aortic muscle A7r5 cell proliferation, respectively.
Western bolt was used to explore the protein expression of H3K9me3 and p53 after 50 nmol/L Chaetocin incubating A7r5 cells for 72 h.Results:Chaetocin can significantly suppressed A7r5 cell proliferation induced by high glucose in a concentration- and time- dependent
manner. Compared with normal concentration of glucose, Chaetocin significantly inhibited the up-regulated expression of H3K9me3 and
increased the down-regulated expression of p53 induced by high glucose in A7r5 cells (P<0.05).Conclusion:Down-regulated p53 can
enhance the proliferation of rat thoracic aortic muscle cell induced by high glucose via H3K9me3, while H3K9 methyltransferase inhibitor
Chaetocin can suppressed this process, which provides a new insight for the treatment of diabetic macroangiopathy. |
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