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结缔组织生长因子小干扰RNA对培养的人腹膜间皮细胞中血管内皮生长因子和结缔组织生长因子表达的抑制作用

Inhibition effect of small interfering RNA of connective tissue growth factor on the expression of vascular endothelial growth factor and connective tissue growth factor in cultured human peritoneal mesothelial cells.

作者信息

Liu Fu-you, Xiao Li, Peng You-ming, Duan Shao-bin, Liu Hong, Liu Ying-hong, Ling Gui-hui, Yuan Fang, Chen Jun-xiang, Fu Xiao, Zhu Jian-lian

机构信息

Division of Nephrology, Second Affiliated Xiangya Hospital, Central South University, Changsha 410002, China.

出版信息

Chin Med J (Engl). 2007 Feb 5;120(3):231-6.

Abstract

BACKGROUND

The peritoneum response to peritoneal dialysis can lead to fibrosis. The transforming growth factor beta1 (TGF-beta1) plays a key role in regulating tissue repair and remodelling after injury. Connective tissue growth factor (CTGF), a downstream mediator of TGF-beta1 inducing fibrosis, has been implicated in peritoneal fibrosis. Vascular endothelial growth factor (VEGF) plays a key role in angiogenesis that can hasten peritoneal fibrosis. In this study, we investigated the effect of small interfering RNA (siRNA) of CTGF by pRETRO-SUPER (PRS) retrovirus vector on the expression of CTGF and VEGF in human peritoneal mesothelial cells.

METHODS

Retrovirus producing CTGF siRNA were constructed from the inverted oligonucleotides and transferred into packaging cell line PT67 with lipofectamine, and the virus supernatant was used to infect human peritoneal mesothelial cell (HPMC). The cells were divided into seven groups: low glucose DMEM, low glucose DMEM + TGF-beta1 5 ng/ml, low glucose DMEM + TGF-beta1 5 ng/ml + PRS-CTGF-siRNA(1-4) and low glucose DMEM + TGF-beta1 5 ng/ml + PRS. The expression of CTGF and VEGF were measured by semiquantitative RT-PCR and Western blot.

RESULTS

Low levels of CTGF and VEGF were detected in confluent HPMCs. Following stimulation with TGF-beta1, the levels of CTGF and VEGF were significantly upregulated (P < 0.01). Introduction of PRS-CTGF-siRNA(1-4) resulted in the significant reduction of CTGF mRNA and protein, and VEGF mRNA (P < 0.01), especially in groups PRS-CTGF-siRNA1 and PRS-CTGF-siRNA4. The introduction of PRS void vector did not have these effects (P > 0.05).

CONCLUSIONS

The expression of CTGF siRNA mediated by PRS retrovirus vector can effectively reduce the level of CTGF and VEGF induced by TGF-beta1 in cultured HPMCs. This study may provide potential therapeutic strategies to prevent the peritoneal fibrosis.

摘要

背景

腹膜对腹膜透析的反应可导致纤维化。转化生长因子β1(TGF-β1)在调节损伤后的组织修复和重塑中起关键作用。结缔组织生长因子(CTGF)是TGF-β1诱导纤维化的下游介质,与腹膜纤维化有关。血管内皮生长因子(VEGF)在可加速腹膜纤维化的血管生成中起关键作用。在本研究中,我们研究了pRETRO-SUPER(PRS)逆转录病毒载体介导的CTGF小干扰RNA(siRNA)对人腹膜间皮细胞中CTGF和VEGF表达的影响。

方法

由反向寡核苷酸构建产生CTGF siRNA的逆转录病毒,并用脂质体转染包装细胞系PT67,病毒上清液用于感染人腹膜间皮细胞(HPMC)。细胞分为七组:低糖DMEM、低糖DMEM + 5 ng/ml TGF-β1、低糖DMEM + 5 ng/ml TGF-β1 + PRS-CTGF-siRNA(1-4)和低糖DMEM + 5 ng/ml TGF-β1 + PRS。通过半定量RT-PCR和Western印迹法检测CTGF和VEGF的表达。

结果

在汇合的HPMC中检测到低水平的CTGF和VEGF。用TGF-β1刺激后,CTGF和VEGF水平显著上调(P < 0.01)。引入PRS-CTGF-siRNA(1-4)导致CTGF mRNA和蛋白以及VEGF mRNA显著降低(P < 0.01),尤其是在PRS-CTGF-siRNA1和PRS-CTGF-siRNA4组。引入PRS空载体没有这些作用(P > 0.05)。

结论

PRS逆转录病毒载体介导的CTGF siRNA表达可有效降低培养的HPMC中TGF-β1诱导的CTGF和VEGF水平。本研究可能为预防腹膜纤维化提供潜在的治疗策略。

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