芍药苷对增殖性瘢痕成纤维细胞增殖抑制作用及机制研究
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河南省省部共建课题项目:自体细胞培养复合型人工真皮的构建及临床应用研究(编号:201401014)。


Inhibitory effect and mechanism of paeoniflorin on proliferation of hypertrophic scar fibroblasts
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    目的 探索芍药苷对增殖性瘢痕(HS)成纤维细胞增殖抑制作用及机制研究。方法 0(对照组),200,400,800 μmol/L的芍药苷作用HS成纤维细胞24、48、72 h后,MTT法检测细胞活力,Hoechst染色法检测细胞凋亡,流式细胞术检测细胞周期,酶联免疫吸附试验(ELISA)检测细胞Ⅰ型胶原(COL Ⅰ)和Ⅲ型胶原(COL Ⅲ)含量,Western blot检测转化生长因子-β(TGF-β)/Smad信号通路相关蛋白及基质金属蛋白酶1(MMP1)、MMP13表达。结果 200,400,800 μmol/L芍药苷能显著降低HS成纤维细胞活力(P< 0.01),使细胞核发白,皱染,使细胞周期阻滞在G1期(P< 0.01),能显著降低细胞中COLⅠ、COLⅢ含量(P< 0.01),下调MMP1、MMP13、TGF-β1、p-Smad2及p-Smad3表达(P< 0.01)。结论 芍药苷能明显抑制HS成纤维细胞增殖及胶原合成,可能是通过抑制TGF-β1/Smad信号通路实现的。

    Abstract:

    Objective To explore the inhibitory effect and related mechanism of paeoniflorin on proliferation of hypertrophic scar (HS) fibroblasts. Methods HS fibroblasts were cultured with 0 (control), 200, 400, 800 μmol/L of paeoniflorin for 24, 48, and 72 h. Cell viability was detected by MTT assay. Cell apoptosis was detected using Hoechst staining. Cell cycle was measured by flow cytometry. The levels of type I collagen (COL I) and type Ⅲ collagen (COL Ⅲ) were detected by enzyme linked immunosorbent assay (ELISA). The expressions of transforming growth factor-β (TGF-β)/Smad signaling pathway related proteins, as well as matrix metalloproteinase 1 (MMP1) and MMP13 were detected by Western blot. Results 200, 400, 800 μmol/L of paeoniflorin reduced the cell viability of HS fibroblasts significantly (P< 0.01), with the nuclei turning pale and shrunken, and caused cell cycle arrest at G1 phase (P< 0.01). Moreover, the levels of COL I and COL Ⅲ in the cells were decreased significantly (P< 0.01), and the expressions of MMP1, MMP13, TGF-β1, p-Smad2 and p-Smad3 were down-regulated significantly (P< 0.01). Conclusions Paeoniflorin can obviously inhibit the proliferation and collagen synthesis of hypertrophic scar fibroblasts, probably through inhibition of the TGF-β1/Smad signaling pathway.

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王雷,马园园,李亚玲,周粤闽.芍药苷对增殖性瘢痕成纤维细胞增殖抑制作用及机制研究[J].中国比较医学杂志,2017,27(11):38~43.

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  • 收稿日期:2017-05-26
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  • 在线发布日期: 2017-11-28
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