Department of Orthopedics, Minhang Hospital, Fudan University, Shanghai 201199, P.R. China.
Int J Mol Med. 2020 Sep;46(3):965-976. doi: 10.3892/ijmm.2020.4651. Epub 2020 Jun 19.
MicroRNAs (miRNAs) are known to have regulatory roles in the osteogenic differentiation of various mesenchymal stem cells (MSCs), although their regulatory role on human adipose‑derived mesenchymal stem cells (hADSCs) remains unclear. The aim of the present study was to investigate the biological function and underlying molecular mechanism of miRNAs in regulating the osteogenic differentiation of hADSCs using microarray assay. hADSCs differentiated into osteoblasts under culture with osteogenic medium, with an increase observed in calcium deposits and alkaline phosphatase activity. The mRNA levels of bone sialoprotein, osteopontin and osteocalcin increased, whereas Runt‑related transcription factor‑2 expression decreased during osteogenic differentiation. In addition, miR‑143 was markedly downregulated during osteogenic differentiation, while miR‑143 overexpression inhibited and miR‑143 knockdown enhanced this process. miR‑143 overexpression also blocked extracellular signal‑regulated kinase 1/2 (ERK1/2) pathway activation, while miR‑143 inhibition enhanced it. The promoting effects of miR‑143 knockdown on the osteogenic differentiation of hADSCs were partly diminished by the mitogen‑activated protein kinase (MEK) inhibitors U0126 and PD98059. Bioinformatics analysis further revealed that miR‑143 targets k‑Ras and directly binds to the 3'‑untranslated region of its mRNA. Inhibition of miR‑143 enhanced the activation of the k‑Ras/MEK/ERK pathway during osteogenic differentiation, whereas miR‑143 overexpression had the opposite effect. Collectively, these results demonstrated that miR‑143 negatively regulates the osteogenic differentiation of hADSCs through the k‑Ras/MEK/ERK pathway, providing further insight into the underlying molecular mechanisms.
微小 RNA(miRNA)已知在各种间充质干细胞(MSC)的成骨分化中具有调节作用,尽管其对人脂肪间充质干细胞(hADSC)的调节作用尚不清楚。本研究旨在通过微阵列分析研究 miRNA 在调节 hADSC 成骨分化中的生物学功能和潜在分子机制。hADSC 在成骨培养基中分化为成骨细胞,观察到钙沉积和碱性磷酸酶活性增加。骨涎蛋白、骨桥蛋白和骨钙素的 mRNA 水平增加,而 Runt 相关转录因子 2 的表达在成骨分化过程中降低。此外,miR-143 在成骨分化过程中明显下调,而 miR-143 过表达抑制,miR-143 敲低增强这一过程。miR-143 过表达还阻断细胞外信号调节激酶 1/2(ERK1/2)通路的激活,而 miR-143 抑制则增强该通路的激活。miR-143 敲低对 hADSC 成骨分化的促进作用部分被丝裂原活化蛋白激酶(MEK)抑制剂 U0126 和 PD98059 减弱。生物信息学分析进一步表明,miR-143 靶向 k-Ras 并直接与其 mRNA 的 3'非翻译区结合。成骨分化过程中,miR-143 抑制增强 k-Ras/MEK/ERK 通路的激活,而 miR-143 过表达则产生相反的效果。综上所述,这些结果表明,miR-143 通过 k-Ras/MEK/ERK 通路负调控 hADSC 的成骨分化,为深入了解潜在的分子机制提供了进一步的依据。