Article Summary
黄敬文,王 景,安丽凤,段剑飞,代 宇,高宏伟.地龙蛋白对人增生性瘢痕细胞增殖抑制作用机制研究[J].现代生物医学进展英文版,2017,17(35):6828-6832.
地龙蛋白对人增生性瘢痕细胞增殖抑制作用机制研究
Earthworm Protein of Hyperplastic Scar Cell Proliferation Inhibition Mechanism Research
Received:August 16, 2017  Revised:September 10, 2017
DOI:10.13241/j.cnki.pmb.2017.35.007
中文关键词: 地龙  HSF细胞  Cyclin D1  Caspase-3  TGF-β1  Bcl-2  Mcl-2
英文关键词: Dragon  HSF cells  Cyclin D1  Caspase-3  TGF-β1  Bcl-2  Mcl-2
基金项目:黑龙江省自然科学基金面上项目(H2015023);黑龙江省博士后管理站课题(LBH-Z13198);黑龙江中医药大学博士创新基金项目(2013bs03)
Author NameAffiliationE-mail
黄敬文 黑龙江中医药大学佳木斯学院 黑龙江 佳木斯 154000 1148739983@qq.com 
王 景 黑龙江中医药大学附属第二医院 黑龙江 哈尔滨 150009  
安丽凤 黑龙江中医药大学佳木斯学院 黑龙江 佳木斯 154000  
段剑飞 黑龙江中医药大学佳木斯学院 黑龙江 佳木斯 154000  
代 宇 黑龙江中医药大学附属第一医院 黑龙江 哈尔滨 150040  
高宏伟 黑龙江中医药大学附属第一医院 黑龙江 哈尔滨 150040  
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中文摘要:
      摘要 目的:研究地龙蛋白对人增生性瘢痕细胞增殖抑制作用机制。方法:培养人增生性瘢痕成纤维细胞(HSF),将传代好的HSF细胞分为四组,分别加入地龙样品浓度为0 mg/mL(对照组)、0.3125 mg/mL(低剂量组)、0.625 mg/mL(中剂量组)、1.25 mg/mL(高剂量组)。应用MTS法检测细胞活力,流式细胞仪检测细胞凋亡率,RT-PCR法和Western -blot法测定Cyclin D1、Caspase-3、TGF-β1的表达,Western -blot法测定Bcl-2、Mcl-2的表达。结果:地龙蛋白对HSF细胞的增殖活力有抑制作用。浓度0.625 mg/mL、1.25 mg/mL样品组作用细胞48 h后凋亡率为分别为31.5 %和69.2 %,(P<0.01);RT-PCR显示,浓度0.625 mg/mL、1.25 mg/mL样品组能够增加Caspase-3的基因表达,降低CyclinD1的基因表达,降低TGF-β1的基因表达,(P<0.01);浓度0.3125 mg/mL样品组与空白对照组比较有显著性差异(P<0.05)。W-B方法显示,各样品组能够增加Caspase-3的蛋白表达量,降低Cy- clinD 1的蛋白表达量,降低TGF-β1的蛋白表达量,(P<0.01);浓度0.625 mg/mL、1.25 mg/mL样品组能够降低Bcl-2蛋白表达量,(P<0.01);浓度0.3125 mg/mL样品组Bcl-2的蛋白表达量与空白对照组比较有显著性差异(P<0.05)。结论:地龙蛋白诱导细胞死亡,作用机制与下调Cyclin D1的基因和蛋白表达,上调Caspase-3的基因和蛋白表达,下调TGF-β1的基因和蛋白表达,下调Bcl-2蛋白表达量有关。
英文摘要:
      ABSTRACT Objective: The mechanism of the proliferation inhibition of hypertrophic scar cells was studied. Methods: Cultured hy- perplastic scar fibroblasts(HSF), HSF cells were divided into four groups after generation, add earthworm sample separately, the concen- tration is 0 mg/mL(The control group), 0.3125 mg/mL(Low dose group), 0.625 mg/mL (Middle dose group), 1.25 mg/mL (High dose group). Cell vitality was detected by MTS method. Cell apoptosis rate was detected by flow cytometry. The expression of Cyclin D1, Caspase - 3 and TGF-β1 was determined by Rt-pcr methodand Western blot method. The expression of bcl-2 and McL-2 was deter- mined by Western - blot method. Results: Earthworm proteinhas inhibitory effect on the proliferation activity of HSF cells. Concentration of 0.625 mg/mL, 1.25 mg/mL sample group effect on the cellseparately after 48 hours, the apoptosis rate of the cell was 31.5% and 69.2%. method showed that concentration of 0.625 mg/mL, 1.25 mg/mL sample group was able to increase gene expression of Cas- pase-3, reduce gene expression of CyclinD1 and TGF -β1(P<0.01). There was a significant difference between the 0.3125 mg/mL sample group and the blank control group (P<0.05). Western - blot method showed that Each sample group could increase the protein expression of Caspase-3, reduce the protein expression of CyclinD1, and reduce the protein expression of TGF-beta 1 (P<0.01). The concentration of 0.625 mg/mL and 1.25 mg/mL samples was able to reduce the expression of bcl-2 protein (P<0.01). The protein expression of bcl-2 in the concentration of 0.3125 mg/mL sample group was significantly different than that in the blank control group (P<0.05). Conclusion: The mechanism of earthworm protein inducing cell death was related to that earthworm protein can cut Cyclin D1 gene and protein expres- sion, raise Caspase 3 gene and protein expression, cut TGF-β1 gene and protein expression, cut the Bcl-2 protein expression quantity.
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