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作 者:邹彤[1] 宋怡[2] 吴伟[3] 李树德[4] 张彦[4]
机构地区:[1]北京医院,北京100730 [2]昆明医学院第一附属医院 [3]卫生部老年病研究所 [4]昆明医学院基础医学院
出 处:《内科急危重症杂志》2008年第3期136-138,共3页Journal of Critical Care In Internal Medicine
基 金:国家自然科学基金资助(No:30560036)
摘 要:目的:研究血管内皮生长因子(VEGF)对同型半胱氨酸所致血管内皮细胞生长停滞的作用及其分子机制。方法:用[3H]-胸腺嘧啶脱氧核苷掺入法测定细胞DNA合成率,基因表达测定采用RT-PCR。结果:①同型半胱氨酸诱导血管内皮细胞生长停滞、CHOP基因表达升高。VEGF能显著地抑制同型半胱氨酸诱导血管内皮细胞生长停滞,但不影响CHOP表达;②VEGF诱导核糖体蛋白RPS3a表达升高;③瞬时转染RPS3a基因抑制诱导血管内皮细胞生长停滞;④PI3K抑制剂wortmannin显著拮抗VEGF的作用,MEK抑制剂PD98059没有影响。结论:VEGF可通过PI3K信号途径上调RPS3a表达,抑制同型半胱氨酸诱导血管内皮细胞生长停滞,提示VEGF是一个潜在的抑制同型半胱氨酸所致动脉粥样硬化的药物。Objective:To investigate the effect of vascular endothelial growth factor (VEGF) on cell growth arrest induced by homocysteine. Methods: DNA synthesis in cells was measured by using [^3 H]-thymidine incorporation. The expression of CHOP and ribosomal protein S3a (RPS3a) were detected by RT-PCR. Results: ① Homocysteine promoted cell growth arrest as well as expression of CHOP in endothelial cells. VEGF significantly inhibited homocysteine-induced endothelial cell growth arrest. However, VEGF did not affect homocysteine-induced CHOP expression. ② VEGF up-regulated the expression of RPS3a. ③ Transient transfection of RPS3a markedly suppressed homocysteine induced endothelial cell growth arrest. ④ PI3K inhibitor wortmannin,rather than MEK inhibitor PD98059, blocked the action of VEGF. Conclusion: The inhibitory effect of VEGF on homocysteine-induced endothelial cell growth arrest was due to its ability to elicit the expression of RPS3a through the PI3K pathway.
关 键 词:同型半胱氨酸 血管内皮细胞 血管内皮生长因子 细胞生长停滞 核糖体蛋白S3a
分 类 号:R541.4[医药卫生—心血管疾病]
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