lncRNA MEG8 Upregulates miR-770-5p Through Methylation and Promotes Cell Apoptosis in Diabetic Nephropathy

被引:21
|
作者
Zhang, Jinmei [1 ]
Song, Liwen [2 ]
Ma, Yanjuan [3 ]
Yin, Yan [1 ]
Liu, Xinqi [1 ]
Luo, Xinyu [1 ]
Sun, Jiali [1 ]
Wang, Liqin [1 ]
机构
[1] Weifang Hosp Tradit Chinese Med, Dept Endocrinol, Weifang 261000, Shandong, Peoples R China
[2] Weifang Peoples Hosp, Dept Endocrinol, Weifang 261000, Shandong, Peoples R China
[3] Sunshine Fus Hosp, Dept Endocrinol, Sunshine 261061, Shandong, Peoples R China
来源
DIABETES METABOLIC SYNDROME AND OBESITY-TARGETS AND THERAPY | 2020年 / 13卷
关键词
diabetic nephropathy; MEG8; miR-770-5p; apoptosis;
D O I
10.2147/DMSO.S255183
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: It has been reported that lncRNA MEG8 can be induced by glucose in mice model of kidney injury, indicating its role in diabetic nephropathy (DN). This study was carried out to explore the role of MEG8 in DN. Materials and Methods: The expression of MEG8 and miR-770-5p in plasma samples from DN patients (n = 66), diabetic patients (DM patients with no complications, n = 66) and healthy controls (n = 66) was detected by RT-qPCR. The interaction between MEG8 and miR-770-5p in podocyte cells was evaluated by transient transfections. Cell apoptosis under high-glucose treatment was detected by cell apoptosis assay. Results: MEG8 and miR-770-5p were upregulated in plasma of DM patients and were further upregulated in DN patients. MEG8 was positively correlated with miR-770-5p. In podocyte cells, high-glucose treatment resulted in increased expression levels of MEG8 and miR-770-5p. In podocyte cells, overexpression of MEG8 resulted in upregulated expression of miR-770-5p and decreased methylation of the miR-770-5p gene. Cell apoptosis analysis showed that overexpression of MEG8 and miR-770-5p resulted in increased cell apoptotic rate under glucose treatment. In addition, combined overexpression of MEG8 and miR-7705-p showed stronger effects. Conclusion: MEG8 may upregulate miR-770-5p through methylation to promote DN by promoting cell apoptosis.
引用
收藏
页码:2477 / 2483
页数:7
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