首页|LINC02695表达在糖尿病视网膜病变新生血管中的初步研究

LINC02695表达在糖尿病视网膜病变新生血管中的初步研究

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目的 探讨长链非编码RNA(lncRNA)LINC02695在高糖(HG)环境下人视网膜微血管内皮细胞(HRMECs)中的表达及其对HRMECs的增殖、迁移及新生血管形成的影响。方法 HRMECs分为4组,分别为正常糖(NG)组(5。5 mmol/L)、HG 组(30。0 mmol/L)、HG+LINC02695 沉默(HG+si-LINC02695)组、HG+沉默对照(HG+si-NC)组。实时荧光定量PCR(qPCR)检测各组HRMECs中LINC02695及VEGF mRNA的表达情况,CCK-8法测定各组细胞的增殖情况,Transwell实验检测各组细胞的迁移能力,管形成实验检测各组细胞的成管能力。结果 qPCR结果显示:与NG组比较,HG组细胞LINC02695、VEGF mRNA呈高表达(P<0。05);与 HG组比较,HG+si-LINC02695组细胞 VEGF mRNA表达水平明显下降(P<0。05)。CCK-8实验结果显示:与NG组比较,HG组细胞增殖能力明显增强(P<0。05);与HG组比较,HG+si-LINC02695组细胞增殖能力明显下降(P<0。05)。Transwell实验结果显示:与NG组比较,HG组细胞迁移能力明显增加(P<0。05);与HG组比较,HG+si-LINC02695组细胞迁移能力明显下降(P<0。05);管形成实验结果显示:与NG组比较,HG组细胞成管能力明显增加(P<0。05);与HG组比较,HG+si-LINC02695组细胞成管能力明显下降(P<0。05)。结论 LINC02695可能参与促进HG诱导下HRMECs的增殖、迁移及血管形成。
Preliminary study on expression of LINC02695 in neovascularization in diabetic retinopathy
Objective To investigate the expression of long non-coding RNA(lncRNA)LINC02695 in human retinal microvascular endothelial cells(HRMECs)in high glucose(HG)environment and its effect on the proliferation,migration and neovascularization of HRMECs.Methods HRMECs was divided into four groups:the normal glucose(NG)group(5.5 mmol/L),the HG group(30.0 mmol/L),the HG+LINC02695 silenced group(HG+si-LINC02695),and the HG+silenced control group(HG+si-NC).Real-time quantita-tive fluorescent PCR(qPCR)was used to detect the expression of LINC02695 and vascular endothelial growth factor(VEGF)mRNA in HRMECs of each group.The cell proliferation of each group was measured by Cell Counting Kit-8(CCK-8)method.The migration ability of cells in each group was detected by Transwell as-say.The tube forming ability of cells in each group was detected by tube forming experiment.Results The qPCR results showed that compared with the NG group,LINC02695 and VEGF were highly expressed in the HG group(P<0.05).Compared with the HG group,VEGF mRNA expression level in the HG+si-LINC02695 group was significantly decreased(P<0.05).The results of CCK-8 experiment showed that the proliferation ability of the HG group was significantly enhanced compared with the NG group(P<0.05).Compared with the HG group,the cell proliferation ability of the HG+si-LINC02695 group was significantly decreased(P<0.05).The results of Transwell experiment showed that the cell migration ability of the HG group was significantly increased compared with the NG group(P<0.05).Compared with the HG group,the cell migration ability of the HG+si-LINC02695 group was significantly decreased(P<0.05).The results of tube formation experiment showed that compared with the NG group,the tube formation ability of the HG group was significantly increased(P<0.05).Compared with the HG group,canalization ability of cells in the HG+si-LINC02695 group was significantly decreased(P<0.05).Conclusion LINC02695 may be involved in promoting the proliferation,migration and angiogenesis of HRMECs induced by HG.

long non-coding RNA LINC02695diabetic retinopathyhuman retinal endothelial cellsproliferationmigrationneovascularization

袁园、朱安民、曾兰、龙小凤、叶萌、唐凯、谭薇

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遵义医科大学第一临床学院,贵州遵义 563000

遵义市第一人民医院/遵义医科大学第三附属医院眼科,贵州遵义 563000

云阳县人民医院眼科,重庆 404500

遵义市第一人民医院/遵义医科大学第三附属医院中心实验室,贵州遵义 563000

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LINC02695 糖尿病视网膜病变 人视网膜内皮细胞 细胞增殖 细胞迁移 新生血管形成

2024

重庆医学
重庆市卫生信息中心,重庆市医学会

重庆医学

CSTPCD
影响因子:1.797
ISSN:1671-8348
年,卷(期):2024.53(4)
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