何书英, 王慧芳, 俞丹凤, 袁静. 肝素寡糖抑制血小板衍生生长因子诱导平滑肌细胞增殖机制的研究J. 药学学报, 2015,50(8): 993-999.
引用本文: 何书英, 王慧芳, 俞丹凤, 袁静. 肝素寡糖抑制血小板衍生生长因子诱导平滑肌细胞增殖机制的研究J. 药学学报, 2015,50(8): 993-999.
HE Shu-ying, WANG Hui-fang, YU Dan-feng, YUAN Jing. The mechanisms of heparin-derived oligosaccharide on the inhibition of smooth muscle cells proliferation induced by platelet-derived growth factorJ. Acta Pharmaceutica Sinica, 2015,50(8): 993-999.
Citation: HE Shu-ying, WANG Hui-fang, YU Dan-feng, YUAN Jing. The mechanisms of heparin-derived oligosaccharide on the inhibition of smooth muscle cells proliferation induced by platelet-derived growth factorJ. Acta Pharmaceutica Sinica, 2015,50(8): 993-999.

肝素寡糖抑制血小板衍生生长因子诱导平滑肌细胞增殖机制的研究

The mechanisms of heparin-derived oligosaccharide on the inhibition of smooth muscle cells proliferation induced by platelet-derived growth factor

  • 摘要: 本实验研究了肝素寡糖 (HDO) 对血小板衍生生长因子 (PDGF) 诱导血管平滑肌细胞 (VSMCs) 增殖的影响, 并对其作用机制进行初步探讨。实验分为空白组、模型组及肝素寡糖组。采用MTT法和流式细胞仪检测HDO对VSMCs增殖活性及其细胞周期分布影响, Western blot、免疫组化和RT-PCR检测PKC、MAPK、Akt/PI3K信号通路中PKC-α、p-Akt、p-ERK1/2、p-GSK-3β和p-PDK1等关键蛋白及c-fosc-mycc-jun等原癌基因的表达水平, 结果显示, HDO (0.01、0.1和1 µmol·L-1) 可浓度依赖性抑制30 ng·mL-1 PDGF诱导的VSMCs增殖活性, 阻滞细胞周期G1/S期转换, 并下调信号通路中关键蛋白及原癌基因表达 (均为P < 0.05)。结果提示, HDO可能通过抑制信号通路中关键蛋白的表达水平从而抑制原癌基因表达和G1/S期转换, 进而抑制VSMCs增殖。

     

    Abstract: In this study, the effect of heparin-derived oligosaccharide (HDO) on platelet-derived growth factor (PDGF) induced vascular smooth muscle cells (VSMCs) proliferation and the related signal transduction mechanisms were investigated. MTT assays were used to measure VSMCs proliferation. Cell cycle distribution was analyzed by flow cytometry. The level of key regulatory proteins in PKC, MAPK and Akt/PI3K pathways were determined by RT-PCR, Western blot and immunocytochemical methods. Meanwhile, mRNA expressions of some proto-oncogenes were assayed by RT-PCR method. Our data showed that HDO (0.01, 0.1 and 1 �mol·L-1) inhibited 30 ng·mL-1 PDGF-induced VSMCs proliferation in a dose-dependent manner, blocked the G1/S transition and inhibited the level of key regulatory proteins and some proto-oncogenes (P < 0.05). The results showed that HDO may decrease the key regulatory proteins expression, hence suppress the transcription of proto-oncogene and G1/S transition, finally inhibiting VSMCs proliferation.

     

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