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微小RNA-205通过靶向趋化素样因子超家族成员4抑制肾细胞凋亡。

MicroRNA-205 inhibits renal cells apoptosis via targeting CMTM4.

作者信息

Zhang Hongxia, Zhang Xiaoning, Yuan Xiaoying, Wang Linna, Xiao Ying

机构信息

Department of Internal Medicine, Shengli Oilfield Central Hospital, Dongying City, Shandong Province, 257034, P. R. China.

出版信息

Iran J Basic Med Sci. 2015 Oct;18(10):1020-6.

Abstract

OBJECTIVES

MicroRNAs (miRNAs) are small non-coding RNA molecules that regulate gene expression. They have important roles in kidney development, homeostasis and disease, and participate in the onset and progression of tubulointerstitial sclerosis and end-stage glomerular lesions that occur in various forms of chronic kidney disease (CKD). In the present study, we elucidated the role of microRNA 205 (miR-205) in cisplatin-induced renal cell apoptosis and explored the molecular mechanisms.

MATERIALS AND METHODS

The chronic interstitial nephropathy rat model was induced, and the miRNA expression profile in the kidney cells from rats with CKD was screened. Cisplatin-induced apoptosis in normal renal HK-2 cells was evaluated using flow cytometry, and regulation of miR-205 on target gene was validated using luciferase assay, western blot and real time PCR assays.

RESULTS

We found that miR-205 expression was significantly decreased in the cells from kidney of CKD rat (P<0.01). Our data showed that when miR-205 was overexpressed or silenced using the mimic or inhibitor, the percentages of apoptotic cells were suppressed or increased significantly (P<0.05), respectively. Moreover, we have identified CMTM4 gene, which is involved in cell proliferation and apoptosis, as a novel target for miR-205. In addition, miR-205 could inhibit apoptosis by binding to the 3'UTR of CMTM4 mRNA and inhibiting its transcriptional activity.

CONCLUSION

This study elucidated that miR-205 plays an important role in the regulation of apoptosis in renal cells, suggesting a potential therapeutic target to hinder CKD development.

摘要

目的

微小RNA(miRNA)是一类调节基因表达的小型非编码RNA分子。它们在肾脏发育、内环境稳定和疾病中发挥重要作用,并参与各种形式的慢性肾脏病(CKD)中发生的肾小管间质纤维化和终末期肾小球病变的发生与发展。在本研究中,我们阐明了微小RNA 205(miR-205)在顺铂诱导的肾细胞凋亡中的作用,并探讨了其分子机制。

材料与方法

建立慢性间质性肾病大鼠模型,筛选CKD大鼠肾细胞中的miRNA表达谱。采用流式细胞术评估顺铂诱导的正常肾HK-2细胞凋亡情况,并通过荧光素酶报告基因检测、蛋白质免疫印迹和实时定量PCR检测验证miR-205对靶基因的调控作用。

结果

我们发现CKD大鼠肾脏细胞中miR-205表达显著降低(P<0.01)。我们的数据表明,当使用模拟物或抑制剂使miR-205过表达或沉默时,凋亡细胞百分比分别显著受到抑制或增加(P<0.05)。此外,我们确定了参与细胞增殖和凋亡的CMTM4基因是miR-205的一个新靶标。此外,miR-205可通过与CMTM4 mRNA的3'非翻译区结合并抑制其转录活性来抑制凋亡。

结论

本研究阐明了miR-205在肾细胞凋亡调控中起重要作用,提示其可能是阻碍CKD发展的潜在治疗靶点。

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