Department of Molecular Biology and Genetics, Aarhus University, Aarhus 8000, Denmark.
Department of Molecular Biology and Genetics, Aarhus University, Aarhus 8000, Denmark; Interdisciplinary Nanoscience Center, Aarhus University, Aarhus 8000, Denmark.
Mol Ther. 2018 Feb 7;26(2):593-605. doi: 10.1016/j.ymthe.2017.11.018. Epub 2017 Dec 5.
Bone remodeling and regeneration are highly regulated multistep processes involving posttranscriptional regulation by microRNAs (miRNAs). Here, we performed a global profiling of differentially expressed miRNAs in bone-marrow-derived skeletal cells (BMSCs; also known as stromal or mesenchymal stem cells) during in vitro osteoblast differentiation. We functionally validated the regulatory effects of several miRNAs on osteoblast differentiation and identified 15 miRNAs, most significantly miR-222 and miR-423, as regulators of osteoblastogenesis. In addition, we tested the possible targeting of miRNAs for enhancing bone tissue regeneration. Scaffolds functionalized with miRNA nano-carriers enhanced osteoblastogenesis in 3D culture and retained this ability at least 2 weeks after storage. Additionally, anti-miR-222 enhanced in vivo ectopic bone formation through targeting the cell-cycle inhibitor CDKN1B (cyclin-dependent kinase inhibitor 1B). A number of additional miRNAs exerted additive osteoinductive effects on BMSC differentiation, suggesting that pools of miRNAs delivered locally from an implanted scaffold can provide a promising approach for enhanced bone regeneration.
骨重塑和再生是高度受调控的多步骤过程,涉及 microRNAs(miRNAs)的转录后调控。在这里,我们对骨髓来源的骨骼细胞(BMSCs;也称为基质或间充质干细胞)在体外成骨分化过程中差异表达的 miRNAs 进行了全面分析。我们对几种 miRNA 对成骨分化的调控作用进行了功能验证,并鉴定出 15 个 miRNAs,其中 miR-222 和 miR-423 是成骨细胞发生的重要调节因子。此外,我们还测试了 miRNA 靶向治疗以增强骨组织再生的可能性。功能化 miRNA 纳米载体的支架增强了 3D 培养中成骨细胞的生成,并且在储存至少 2 周后仍保持这种能力。此外,抗 miR-222 通过靶向细胞周期抑制剂 CDKN1B(周期蛋白依赖性激酶抑制剂 1B)增强体内异位骨形成。许多其他 miRNAs 对 BMSC 分化表现出相加的成骨诱导作用,这表明从植入支架局部递送的 miRNA 库可以为增强骨再生提供一种有前途的方法。