首页|2型糖尿病来源外泌体转运circ_001895对高糖胁迫下内皮祖细胞功能的影响

2型糖尿病来源外泌体转运circ_001895对高糖胁迫下内皮祖细胞功能的影响

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目的:探讨 2 型糖尿病(T2DM)来源的外泌体(EXO)中转运环状 RNA_001895(circ_001895)对高糖胁迫下内皮祖细胞的增殖、凋亡、迁移及血管生成标志物的影响。方法:从 T2DM 患者中获取血清样本,分为血清组和EXO组。采用RT-qPCR 技术检测血清和 EXO 中 circ_001895 的表达水平。将T2DM患者血清来源的EXO中circ_001895 表达显著升高的 EXO 命名为 EXO-circ。使用武汉普诺赛公司提供的内皮祖细胞进行培养,并分为以下 3 组:Ctrl 组:常规培养 24h,不进行额外处理。高糖(HG)组:以30mmoL/L葡萄糖处理细胞24h。HG+EXO-circ 组:以 30mmoL/L葡萄糖联合 100μg/mL的EXO-circ处理细胞24h。采用RT-qPCR技术检测各组细胞中circ_001895 的表达。使用CCK-8法检测细胞增殖活力。通过流式细胞术检测细胞凋亡情况。利用 Western blot 技术检测血管生成标志物E-钙黏蛋白(E-cadherin)、N-钙黏蛋白(N-cadherin)和波形蛋白(Vimentin)的表达。通过 Transwell细胞迁移实验检测细胞的迁移能力。结果:与血清组相比,EXO组中circ_001895 的相对表达量显著上调(P<0。05)。与Ctrl组相比,HG组中circ_001895 和E-cadherin的相对表达量及细胞凋亡率均显著上调(均P<0。05),而细胞增殖活力、迁移能力以及N-cadherin 和Vimentin 的相对表达量均显著下调(均P<0。05)。与HG组相比,HG+EXO-circ组中circ_001895 和E-cadherin的相对表达量及细胞凋亡率均显著上调(均P<0。05),而细胞增殖活力、迁移能力以及N-cadherin和Vimentin的相对表达量均显著下调(均P<0。05)。结论:T2DM 来源的 EXO 转运 circ_001895 抑制高糖胁迫下内皮祖细胞的增殖、迁移以及血管生成,并促进细胞的凋亡。
Effect of Exosomal Transport of circ_001895 from Type 2 Diabetes Mellitus on Endothelial Progenitor Cells under High Glucose Stress
Objective:To investigate the effects of exosomal circ_001895 transportation on endothelial progenitor cells under high glucose stress derived from patients with type 2 diabetes(T2DM).Methods:Ser-um samples were obtained from T2DM patients and divided into serum group and EXO group.The expression levels of circ_001895 in serum and EXO were detected by using RT-qPCR technology.EXOs derived from T2DM patients'serum with significantly elevated circ_001895 expression were named EXO-circ.Endothelial progenitor cells provided by Wuhan Procell were cultured and divided into the following three groups.Control Group:Cultured conventionally for 24 hours without additional treatment.High Glucose(HG)Group:Trea-ted with 30 mmoL/L glucose for 24 hours.HG+EXO-circ Group:Treated with 30 mmoL/L glucose combined with 100μg/mL EXO-circ for 24 hours.The expression of circ_001895 in each group of cells was detected u-sing RT-qPCR technology.Cell proliferation vitality was detected using the CCK-8 method.Cell apoptosis was detected using flow cytometry.The expression of angiogenic markers E-cadherin,N-cadherin,and Vim-entin was detected using Western blot technology.Cell migration capacity was detected using the Transwell cell migration assay.Results:Compared to the serum group,the relative expression level of circ_001895 in the EXO group was significantly upregulated(P<0.05).Compared to the control group,the relative expres-sion levels of circ_001895 and E-cadherin and the cell apoptosis rate in the HG group were significantly up-regulated(all P<0.05),while cell proliferation vitality,migration capacity,and the relative expression levels of N-cadherin and Vimentin were significantly downregulated(all P<0.05).Compared to the HG group,the relative expression levels of circ_001895 and E-cadherin and the cell apoptosis rate in the HG+EXO-circ group were significantly upregulated(all P<0.05),while cell proliferation vitality,migration capacity,and the relative expression levels of N-cadherin and Vimentin were significantly downregulated(all P<0.05).Conclusion:Transportation of circ_001895 in exosomes from T2DM inhibits proliferation,migration,and vas-cular generation of endothelial progenitor cells under high glucose stress,while promoting apoptosis.

Type 2 diabetesExosomescirc_001895Endothelial progenitor cellsMigra-tionVascular generation

张洁、张丽、王晨菲、罗荔

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新疆医科大学第五附属医院内分泌科,新疆 乌鲁木齐 830000

2型糖尿病 外泌体 环状RNA_001895 内皮祖细胞 迁移 血管生成

新疆维吾尔自治区自然科学基金

2021D01C437

2024

河北医学
河北省医学会

河北医学

CSTPCD
影响因子:1.915
ISSN:1006-6233
年,卷(期):2024.30(10)