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Reduced mRNA and Protein Expression Levels of Tet Methylcytosine Dioxygenase 3 in Endothelial Progenitor Cells of Patients of Type 2 Diabetes With Peripheral Artery Disease

机译:2型糖尿病合并外周动脉疾病患者内皮祖细胞中Tet甲基胞嘧啶双加氧酶3的mRNA和蛋白质表达水平降低

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摘要

Endothelial progenitor cells (EPCs) with immunological properties repair microvasculature to prevent the complications in patients with diabetes. Epigenetic changes such as DNA methylation alter the functions of cells. Tet methylcytosine dioxygenases (TETs) are enzymes responsible for the demethylation of cytosine on genomic DNA in cells. We hypothesized that EPCs of diabetic patients with peripheral artery disease (D-PAD) might have altered expression levels of TETs. Subjects who were non-diabetic (ND, n = 22), with diabetes only (D, n = 29) and with D-PAD (n = 22) were recruited for the collection of EPCs, which were isolated and subjected to analysis. The mRNA and protein expression levels of TET1, TET2, and TET3 were determined using real-time PCR and immunoblot, respectively. The TET1 mRNA expression level in ND group was lower than that in the D and D-PAD groups. The TET3 mRNA level in the ND group was higher than that in the D group, which was higher than that in the D-PAD group. The TET1 protein level in the D-PAD group, but not the D group, was higher than that in the ND group. The TET2 protein level in the D-PAD group, but not the D group, was lower than that in the ND group. The TET3 protein level in the ND group was higher than that in the D group, which was higher than that in the D-PAD group, which is the lowest among the three groups. The changes of TETs protein levels were due to the alterations of their transcripts. These probably lead to epigenetic changes, which may be responsible for the reductions of EPCs numbers and functions in patients with the D-PAD. The expression pattern of TET3 mRNA and TET3 protein in EPCs may be a biomarker of angiopathy in diabetic patients.
机译:具有免疫特性的内皮祖细胞(EPC)可以修复微血管,以预防糖尿病患者的并发症。表观遗传学改变(例如DNA甲基化)会改变细胞的功能。 Tet甲基胞嘧啶双加氧酶(TET)是负责细胞中基因组DNA上的胞嘧啶脱甲基化的酶。我们假设患有糖尿病的外周动脉疾病(D-PAD)患者的EPC可能改变了TET的表达水平。招募非糖尿病(ND,n = 22),仅患有糖尿病(D,n = 29)和患有D-PAD(n = 22)的受试者收集EPC,将其分离并进行分析。使用实时PCR和免疫印迹分别测定TET1,TET2和TET3的mRNA和蛋白表达水平。 ND组的TET1 mRNA表达水平低于D组和D-PAD组。 ND组的TET3 mRNA水平高于D组,高于D-PAD组。 D-PAD组而非D组的TET1蛋白水平高于ND组。 D-PAD组而非D组的TET2蛋白水平低于ND组。 ND组的TET3蛋白水平高于D组,高于D-PAD组,是三组中最低的。 TETs蛋白水平的变化是由于其转录本的变化。这些可能导致表观遗传学改变,这可能是D-PAD患者EPC数量和功能下降的原因。 EPCs中TET3 mRNA和TET3蛋白的表达模式可能是糖尿病患者血管病变的生物标志物。

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