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槲皮素通过环状RNA调节雌激素受体α介导的骨髓间充质干细胞分化。

Quercetin regulates ERα mediated differentiation of BMSCs through circular RNA.

作者信息

Li Xiaoyun, Chen Rumeng, Lei Xiaotong, Wang Panpan, Zhu Xiaofeng, Zhang Ronghua, Yang Li

机构信息

College of Traditional Chinese Medicine, Jinan University, 601 Huangpu Avenue West, Guangzhou, Guangdong 510632, PR China.

College of Pharmacy, Jinan University, 601 Huangpu Avenue West, Guangzhou, Guangdong 510632, PR China.

出版信息

Gene. 2021 Feb 15;769:145172. doi: 10.1016/j.gene.2020.145172. Epub 2020 Oct 13.

Abstract

Circular RNA (circRNA) participates in regulation of gene transcription, while estrogen receptor alpha (ERα) and quercetin (QUE) positively regulate bone formation, but little is known about the correlation among circRNA, ERα and QUE. In this experiment, we created an ERα-deficient rBMSC model treated with QUE and evaluated the effects of ERα or QUE on rBMSCs, then analyzed differentially-expressed circRNAs by RNA-Seq and bioinformatics. The results showed that ERα deficiency constrained osteogenic differentiation and stimulated adipocytic differentiation of rBMSCs, while QUE abrogated those effects. We identified 136 differentially-expressed circRNAs in the Lv-shERα group and 120 differentially-expressed circRNAs in the Lv-shERα + QUE group. Thirty-two circRNAs retroregulated by ERα and QUE were involved in Rap1 and Wnt signaling, and four of them together sponged miR-326-5p, the target genes of which are osteogenic and adipogenic differentiation factors. Further study showed that over-expressed miR-326-5p could stimulate osteogenic differentiation, while attenuating adipogenic differentiation of rBMSCs. Therefore, we concluded that ERα and QUE might regulate the differentiation of rBMSCs through the circRNA-miR-326-5p-mRNA axis.

摘要

环状RNA(circRNA)参与基因转录调控,而雌激素受体α(ERα)和槲皮素(QUE)对骨形成起正向调节作用,但circRNA、ERα和QUE之间的相关性尚不清楚。在本实验中,我们构建了用QUE处理的ERα缺陷型大鼠骨髓间充质干细胞(rBMSC)模型,评估ERα或QUE对rBMSCs的影响,然后通过RNA测序和生物信息学分析差异表达的circRNA。结果表明,ERα缺陷抑制了rBMSCs的成骨分化并促进了其脂肪细胞分化,而QUE消除了这些影响。我们在Lv-shERα组中鉴定出136个差异表达的circRNA,在Lv-shERα + QUE组中鉴定出120个差异表达的circRNA。由ERα和QUE反向调控的32个circRNA参与Rap1和Wnt信号通路,其中4个共同吸附miR-326-5p,其靶基因是成骨和成脂分化因子。进一步研究表明,过表达miR-326-5p可促进rBMSCs的成骨分化,同时减弱其脂肪生成分化。因此,我们得出结论,ERα和QUE可能通过circRNA-miR-326-5p-mRNA轴调节rBMSCs的分化。

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