Department of Biomedical Engineering, School of Intelligent Medicine and Biotechnology, Guilin Medical University, No. 1 Zhiyuan Road, Lingui District, Guilin, 541199, Guangxi, People's Republic of China.
Education Department of Guangxi Zhuang Autonomous Region, Key Laboratory of Biochemistry and Molecular Biology (Guilin Medical University), No. 1 Zhiyuan Road, Lingui District, Guilin, 541199, Guangxi, People's Republic of China.
Biomed Eng Online. 2024 May 5;23(1):44. doi: 10.1186/s12938-024-01237-9.
Osteocytes are critical mechanosensory cells in bone, and mechanically stimulated osteocytes produce exosomes that can induce osteogenesis. MicroRNAs (miRNAs) are important constituents of exosomes, and some miRNAs in osteocytes regulate osteogenic differentiation; previous studies have indicated that some differentially expressed miRNAs in mechanically strained osteocytes likely influence osteoblastic differentiation. Therefore, screening and selection of miRNAs that regulate osteogenic differentiation in exosomes of mechanically stimulated osteocytes are important.
A mechanical tensile strain of 2500 με at 0.5 Hz 1 h per day for 3 days, elevated prostaglandin E2 (PGE2) and insulin-like growth factor-1 (IGF-1) levels and nitric oxide synthase (NOS) activity of MLO-Y4 osteocytes, and promoted osteogenic differentiation of MC3T3-E1 osteoblasts. Fourteen miRNAs differentially expressed only in MLO-Y4 osteocytes which were stimulated with mechanical tensile strain, were screened, and the miRNAs related to osteogenesis were identified. Four differentially expressed miRNAs (miR-1930-3p, miR-3110-5p, miR-3090-3p, and miR-3058-3p) were found only in mechanically strained osteocytes, and the four miRNAs, eight targeted mRNAs which were differentially expressed only in mechanically strained osteoblasts, were also identified. In addition, the mechanically strained osteocyte-derived exosomes promoted the osteoblastic differentiation of MC3T3-E1 cells in vitro, the exosomes were internalized by osteoblasts, and the up-regulated miR-3110-5p and miR-3058-3p in mechanically strained osteocytes, were both increased in the exosomes, which was verified via reverse transcription quantitative polymerase chain reaction (RT-qPCR).
In osteocytes, a mechanical tensile strain of 2500 με at 0.5 Hz induced the fourteen differentially expressed miRNAs which probably were in exosomes of osteocytes and involved in osteogenesis. The mechanically strained osteocyte-derived exosomes which contained increased miR-3110-5p and miR-3058-3p (two of the 14 miRNAs), promoted osteoblastic differentiation.
成骨细胞是骨骼中关键的机械感受细胞,受机械刺激的成骨细胞会产生能够诱导成骨的外泌体。微小 RNA(miRNA)是外泌体的重要组成部分,成骨细胞中的一些 miRNA 调节成骨细胞分化;先前的研究表明,机械应变的成骨细胞中一些差异表达的 miRNA 可能影响成骨细胞分化。因此,筛选和选择调节机械刺激成骨细胞外泌体中成骨分化的 miRNA 非常重要。
每天施加 2500 με 的机械张应变,频率为 0.5 Hz,持续 1 小时,持续 3 天,可提高 MLO-Y4 成骨细胞中前列腺素 E2(PGE2)和胰岛素样生长因子 1(IGF-1)水平和一氧化氮合酶(NOS)活性,并促进 MC3T3-E1 成骨细胞的成骨分化。筛选出仅在受机械张应变刺激的 MLO-Y4 成骨细胞中差异表达的 14 个 miRNA,并鉴定与成骨相关的 miRNA。发现 4 个差异表达的 miRNA(miR-1930-3p、miR-3110-5p、miR-3090-3p 和 miR-3058-3p)仅在机械应变的成骨细胞中表达,还鉴定了 8 个仅在机械应变的成骨细胞中差异表达的靶向 mRNAs。此外,机械应变的成骨细胞衍生的外泌体在体外促进 MC3T3-E1 细胞的成骨细胞分化,外泌体被成骨细胞内化,并且在机械应变的成骨细胞中上调的 miR-3110-5p 和 miR-3058-3p 在外泌体中均增加,这通过逆转录定量聚合酶链反应(RT-qPCR)得到验证。
在成骨细胞中,2500 με 的机械张应变以 0.5 Hz 诱导 14 个差异表达的 miRNA,这些 miRNA 可能存在于成骨细胞的外泌体中并参与成骨。包含增加的 miR-3110-5p 和 miR-3058-3p(14 个 miRNA 中的两个)的机械应变的成骨细胞衍生的外泌体促进成骨细胞分化。