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A circRNA-miRNA-mRNA network plays a role in the protective effect of diosgenin on alveolar bone loss in ovariectomized rats

机译:Circrna-miRNA-mRNA网络在Diosgenin对卵巢切除大鼠肺泡骨质损失的保护作用起作用

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The present study aimed to assess the perturbation in circular RNA (circRNA)/mRNA expression profiles and a circRNA-miRNA-mRNA coexpression network involved in the potential protective effect of diosgenin (DIO) on alveolar bone loss in rats subjected to ovariectomy (OVX). The Wistar rats (female) manipulated with sham operation were classified as the SHAM group and the grouping of OVX rats administered with DIO, estradiol valerate or vehicle for 12?weeks was DIO group, EV group and OVX group respectively. Following treatments, the plasmatic levels of osteocalcin and tumor necrosis factor-alpha and the microstructure of alveolar bone were assayed. Based on microarray analyses, we identified differentially expressed (DE) circRNAs and mRNAs in alveolar bone of rats in both OVX and DIO group. The DE circRNAs and DE mRNAs involved in the bone metabolism pathway validated by RT-qPCR were considered key circRNAs/mRNAs. On the basis of these key circRNAs/mRNAs, we predicted the overlapping relative miRNAs of key circRNAs/mRNAs, and a circRNA-miRNA-mRNA network was built. DIO showed an anti-osteopenic effect on the rat alveolar bone loss induced by OVX. In total, we found 10 DE circRNAs (6 downregulated and 4 upregulated) and 614 DE mRNAs (314 downregulated and 300 upregulated) in samples of the DIO group compared with those of the OVX group. However, only one circRNA (rno_circRNA_016717) and seven mRNAs (Sfrp1, Csf1, Il1rl1, Nfatc4, Tnfrsf1a, Pik3c2g, and Wnt9b) were validated by qRT-PCR and therefore considered key circRNA/mRNAs. According to these key circRNA/mRNAs and overlapping predicted miRNAs, a coexpression network was constructed. After network analysis, one circRNA-miRNA-mRNA axis (circRNA_016717/miR-501-5p/Sfrp1) was identified. The mechanism of DIO inhibiting alveolar bone loss after OVX is possibly relevant to the simultaneous inhibition of osteogenesis and osteoclastogenesis by mediating the expression of important molecules in the Wnt, PI3K, RANK/RANKL or osteoclastogenic cytokine pathways. The circRNA_016717/miR-501-5p/Sfrp1 axis may play important roles in these processes.
机译:本研究旨在评估循环RNA(CircrNA)/ mRNA表达谱的扰动和CircrNA-miRNA-mRNA共表达网络,涉及Diosgenin(DIO)潜在保护作用的潜在保护作用(DIO)对受卵巢切除术(OVX)的大鼠肺泡骨质损失。用假手术操纵的Wistar大鼠(雌性)被归类为假组,分别使用DIO,雌二醇戊二醇或载体施用的OVX大鼠12?周为DIO组,EV组和OVX组。治疗后,测定骨钙蛋白和肿瘤坏死因子-α的血浆水平和肺泡骨的微观结构。基于微阵列分析,我们在OVX和DIO组的大鼠的肺泡骨中鉴定了差异表达(de)Circrnas和MRNA。涉及通过RT-QPCR验证的骨代谢途径的DE Circrnas和DE MRNA被认为是关键的Circrnas / MRNA。在这些关键的CircRNA / mRNA的基础上,我们预测了关键Circrnas / mRNA的重叠相对miRNA,并且建立了Circrna-miRNA-mRNA网络。 DIO对OVX诱导的大鼠肺泡骨质损失表现出抗骨质作用。与OVX组相比,我们共发现10 de Circrnas(6个下调和4个上调和4个上调的414个上调和300上调的300个)。然而,通过QRT-PCR验证只有一个CircrNA(RNO_CircrNA_016717)和七个MRNA(SFRP1,CSF1,IL1,NFATC4,TNFRSF1,PIK3C2G和WNT9B),因此认为键CircRNA / MRNA。根据这些关键的CircRNA / MRNA和重叠预测的MIRNA,构建了共同表达网络。网络分析后,鉴定了一种CircRNA-miRNA-mRNA轴(CircRNA_016717 / miR-501-5P / SFRP1)。 DIO抑制OVX后抑制肺泡骨质损失的机制可能与同时抑制骨肉发生和骨细胞发生,通过介导WNT,PI3K,RANKL或疏松骨细胞源细胞因子途径的重要分子的表达。 CircRNA_016717 / MIR-501-5P / SFRP1轴可能在这些过程中发挥重要作用。

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