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miR-128-3p 抑制骨髓间充质基质细胞向成骨细胞分化的机制。

Mechanisms of miR‑128‑3p in inhibiting osteoblast differentiation from bone marrow‑derived mesenchymal stromal cells.

机构信息

Department of Orthopedic Surgery, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai Jiao Tong University, Shanghai 200233, P.R. China.

Engineering Research Center of Cell and Therapeutic Antibody, Ministry of Education, School of Pharmacy, Shanghai Jiao Tong University, Shanghai 200240, P.R. China.

出版信息

Mol Med Rep. 2020 Dec;22(6):5041-5052. doi: 10.3892/mmr.2020.11600. Epub 2020 Oct 14.

Abstract

The authors' previous study demonstrated that miR‑128 may exert an inhibitory effect on the osteogenic differentiation of bone marrow‑derived mesenchymal stem cells (BM‑MSCs), but its downstream mechanisms remain to be elucidated. The aim of the present study was to investigate the microRNA (miRNA/miR) and mRNA profiles of differentiated and undifferentiated BM‑MSCs and explore new downstream targets for miR‑128. The sequencing datasets of GSE107279 (miRNA) and GSE112318 (mRNA) were downloaded from the Gene Expression Omnibus database. The differentially expressed miRNAs (DEMs) and genes (DEGs) were identified using the DESeq2 method. The target genes of DEMs were predicted by the miRwalk 2.0 database. The hub target genes of miR‑128 were screened by constructing the protein‑protein interaction (PPI) network and module analysis. The expression levels of miR‑128 and crucial target genes were validated by reverse transcription‑quantitative (RT‑q) PCR before or after transfection of miR‑128 mimics to BM‑MSCs. The miRNA expression profile analysis identified miR‑128 as one of the significantly downregulated DEMs (total 338) in differentiated BM‑MSCs compared with the undifferentiated control. A total of 103 predicted target genes of miR‑128‑3p were overlapped with upregulated DEGs. By calculating the topological properties of each protein in the PPI network, 6 upregulated genes (KIT, NTRK2, YWHAB, GAB1, AXIN1 and RUNX1; fold change was the highest for NTRK2) were considered to be hub genes. Of these, 4 were enriched in module 4 (RUNX1, KIT, GAB1 and AXIN1; RUNX1 was particularly crucial as it can interact with the others), while one was enriched in module 7 (YWHAB). The expression levels of miR‑128 and these 6 target genes during the osteogenic differentiation were experimentally confirmed by RT‑qPCR. In addition, the expression levels of these 6 genes were significantly reversed after transfection of miR‑128‑3p mimics into rat BM‑MSCs compared with the miR‑control group. These findings indicated that miR‑128‑3p may inhibit the osteoblast differentiation of BM‑MSCs by downregulation of these 6 genes, particularly RUNX1, YWHAB and NTRK2.

摘要

作者之前的研究表明,miR-128 可能对骨髓间充质干细胞(BM-MSCs)的成骨分化产生抑制作用,但具体的下游机制仍有待阐明。本研究旨在探讨分化和未分化 BM-MSCs 的 miRNA(miRNA/miR)和 mRNA 谱,并探索 miR-128 的新下游靶点。从基因表达综合数据库(GEO)中下载 GSE107279(miRNA)和 GSE112318(mRNA)数据集。使用 DESeq2 方法鉴定差异表达的 miRNAs(DEMs)和基因(DEGs)。通过 miRwalk 2.0 数据库预测 DEMs 的靶基因。通过构建蛋白质-蛋白质相互作用(PPI)网络和模块分析筛选 miR-128 的枢纽靶基因。在转染 miR-128 模拟物之前或之后,通过逆转录-定量(RT-q)PCR 验证 BM-MSCs 中 miR-128 和关键靶基因的表达水平。miRNA 表达谱分析表明,与未分化对照相比,分化的 BM-MSCs 中 miR-128 是显著下调的 DEMs(共 338 个)之一。miR-128-3p 的 103 个预测靶基因与上调的 DEGs 重叠。通过计算 PPI 网络中每个蛋白质的拓扑特性,发现 6 个上调基因(KIT、NTRK2、YWHAB、GAB1、AXIN1 和 RUNX1;NTRK2 的倍数变化最高)被认为是枢纽基因。其中,4 个基因富集在模块 4(RUNX1、KIT、GAB1 和 AXIN1;RUNX1 尤为关键,因为它可以与其他基因相互作用),而 1 个基因富集在模块 7(YWHAB)。通过 RT-qPCR 实验证实,miR-128 和这 6 个靶基因在成骨分化过程中的表达水平。此外,与 miR-对照相比,转染 miR-128-3p 模拟物后,大鼠 BM-MSCs 中这 6 个基因的表达水平明显逆转。这些发现表明,miR-128-3p 可能通过下调这 6 个基因(特别是 RUNX1、YWHAB 和 NTRK2)抑制 BM-MSCs 的成骨分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6827/7646956/184eb55a7d1d/MMR-22-06-5041-g00.jpg

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