小 RNA 测序揭示了在 hMSCs 成脂肪分化过程中发挥重要作用的新型 tsRNA-06018。

IF 5.3 2区 医学 Q1 Biochemistry, Genetics and Molecular Biology
Journal of Cellular and Molecular Medicine Pub Date : 2020-11-01 Epub Date: 2020-09-16 DOI:10.1111/jcmm.15858
Tao Wang, Lingling Cao, Shan He, Kai Long, Xinping Wang, Hui Yu, Baicheng Ma, Xiaoyuan Xu, Weidong Li
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引用次数: 0

摘要

转运核糖核酸衍生小核糖核酸(tsRNA)是一种新型的非编码核糖核酸衍生物,能够调控多种生物过程。这些 tsRNAs 在调控人骨髓间充质干细胞(hMSCs)成脂肪分化过程中发挥什么作用仍不确定。我们诱导了人骨髓间充质干细胞(hMSCs)的致脂肪分化,然后进行了小 RNA 转录组测序,结果根据 tsRNA 的表达谱确定了 tsRNA-06018 作为感兴趣的靶标。当tsRNA-06018被敲除后,脂肪生成受到抑制,脂肪生成标志物表达减少。当过量表达 STC2 时,会影响这些细胞的成脂分化。我们进一步使用荧光素酶报告实验证实,tsRNA-06018 可直接结合 STC2 的 3'- 非翻译区(3'-UTR)。此外,我们还确定,敲除 tsRNA-06018 和过表达 STC2 都会增加细胞内细胞外信号调节激酶 1/2(ERK1/2)的磷酸化。我们还评估了与单独敲除 tsRNA-06018 相比,加入 ERK1/2 抑制剂 U0126 后,敲除 tsRNA-06018 的 hMSCs 成脂肪分化进一步增强。综上所述,我们利用小 RNA 测序分析了脂肪生成过程中 hMSCs 中的 tsRNA,从而发现 tsRNA-06018 是这一分化过程的新型调控因子。该tsRNA能够通过ERK1/2信号通路靶向STC2,从而调控成脂分化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Small RNA sequencing reveals a novel tsRNA-06018 playing an important role during adipogenic differentiation of hMSCs.

Small RNA sequencing reveals a novel tsRNA-06018 playing an important role during adipogenic differentiation of hMSCs.

Small RNA sequencing reveals a novel tsRNA-06018 playing an important role during adipogenic differentiation of hMSCs.

Small RNA sequencing reveals a novel tsRNA-06018 playing an important role during adipogenic differentiation of hMSCs.

Transfer RNA-derived small RNAs (tsRNAs), a novel type of non-coding RNA derivative, are able to regulate a wide range of biological processes. What role these tsRNAs play in the regulation of human bone marrow mesenchymal stem cell (hMSCs) adipogenic differentiation remains uncertain. We induced the adipogenic differentiation of human bone marrow mesenchymal cells (hMSCs) and then performed small RNA transcriptomic sequencing, leading us to identify tsRNA-06018 as a target of interest based upon resultant the tsRNA expression profiles. When tsRNA-06018 was knocked down, this led to the inhibition of adipogenesis and a decrease in adipogenic marker expression. When STC2 was overexpressed, this impaired the adipogenic differentiation of these cells. We further used luciferase reporter assays to confirm that tsRNA-06018 directly binds the 3'-untranslated region (3'-UTR) of STC2. In addition, we determined that both knocking down tsRNA-06018 and overexpressing STC2 increased extracellular signal-regulated kinase 1/2 (ERK1/2) phosphorylation within cells. We also assessed that the adipogenic differentiation of hMSCs in which tsRNA-06018 was knocked down was further enhanced upon the addition of the ERK1/2 inhibitor U0126 as compared tsRNA-06018 knockdown alone. Taken together, using small RNA sequencing we profiled tsRNAs in hMSCs during the process of adipogenesis, leading us to identify tsRNA-06018 as a novel regulator of this differentiation process. This tsRNA was able to regulate adipogenic differentiation by targeting STC2 via the ERK1/2 signalling pathway.

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来源期刊
CiteScore
10.00
自引率
1.90%
发文量
496
审稿时长
28 weeks
期刊介绍: Bridging physiology and cellular medicine, and molecular biology and molecular therapeutics, Journal of Cellular and Molecular Medicine publishes basic research that furthers our understanding of the cellular and molecular mechanisms of disease and translational studies that convert this knowledge into therapeutic approaches.
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