Mechanically strained osteocyte-derived exosomes contained miR-3110-5p and miR-3058-3p and promoted osteoblastic differentiation

IF 2.9 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Yingwen Zhu, Yanan Li, Zhen Cao, Jindong Xue, Xiaoyan Wang, Tingting Hu, Biao Han, Yong Guo
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引用次数: 0

Abstract

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.
机械拉伸骨细胞衍生的外泌体含有 miR-3110-5p 和 miR-3058-3p,可促进成骨细胞分化
骨细胞是骨骼中重要的机械感觉细胞,受到机械刺激的骨细胞产生的外泌体可诱导成骨。微RNA(miRNA)是外泌体的重要组成成分,而成骨细胞中的一些miRNA可调控成骨分化;先前的研究表明,机械刺激成骨细胞中一些差异表达的miRNA可能会影响成骨细胞的分化。因此,筛选和选择机械刺激成骨细胞外泌体中调控成骨分化的 miRNA 非常重要。连续3天、每天1小时、每小时0.5赫兹、2500με的机械拉伸应变可提高MLO-Y4成骨细胞的前列腺素E2(PGE2)和胰岛素样生长因子-1(IGF-1)水平及一氧化氮合酶(NOS)活性,并促进MC3T3-E1成骨细胞的成骨分化。研究人员筛选了仅在机械拉伸应变刺激下的MLO-Y4成骨细胞中差异表达的14个miRNA,并确定了与成骨相关的miRNA。发现了仅在机械拉伸成骨细胞中差异表达的 4 个 miRNA(miR-1930-3p、miR-3110-5p、miR-3090-3p 和 miR-3058-3p),同时还鉴定了仅在机械拉伸成骨细胞中差异表达的 4 个 miRNA 和 8 个靶 mRNA。此外,机械拉伸成骨细胞衍生的外泌体在体外促进了 MC3T3-E1 细胞的成骨分化,外泌体被成骨细胞内化,机械拉伸成骨细胞中上调的 miR-3110-5p 和 miR-3058-3p 在外泌体中均有增加,这一点通过逆转录定量聚合酶链反应(RT-qPCR)得到了验证。在成骨细胞中,2500 με、0.5 Hz的机械拉伸应变诱导了14种不同表达的miRNA,这些miRNA可能存在于成骨细胞的外泌体中,并参与成骨过程。机械拉伸成骨细胞衍生的外泌体含有更多的miR-3110-5p和miR-3058-3p(14个miRNA中的两个),促进了成骨细胞的分化。
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来源期刊
BioMedical Engineering OnLine
BioMedical Engineering OnLine 工程技术-工程:生物医学
CiteScore
6.70
自引率
2.60%
发文量
79
审稿时长
1 months
期刊介绍: BioMedical Engineering OnLine is an open access, peer-reviewed journal that is dedicated to publishing research in all areas of biomedical engineering. BioMedical Engineering OnLine is aimed at readers and authors throughout the world, with an interest in using tools of the physical and data sciences and techniques in engineering to understand and solve problems in the biological and medical sciences. Topical areas include, but are not limited to: Bioinformatics- Bioinstrumentation- Biomechanics- Biomedical Devices & Instrumentation- Biomedical Signal Processing- Healthcare Information Systems- Human Dynamics- Neural Engineering- Rehabilitation Engineering- Biomaterials- Biomedical Imaging & Image Processing- BioMEMS and On-Chip Devices- Bio-Micro/Nano Technologies- Biomolecular Engineering- Biosensors- Cardiovascular Systems Engineering- Cellular Engineering- Clinical Engineering- Computational Biology- Drug Delivery Technologies- Modeling Methodologies- Nanomaterials and Nanotechnology in Biomedicine- Respiratory Systems Engineering- Robotics in Medicine- Systems and Synthetic Biology- Systems Biology- Telemedicine/Smartphone Applications in Medicine- Therapeutic Systems, Devices and Technologies- Tissue Engineering
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