脚手架
骨愈合
间充质干细胞
血管生成
细胞生物学
材料科学
生物医学工程
体内
再生(生物学)
碱性磷酸酶
化学
癌症研究
解剖
医学
生物
生物化学
生物技术
酶
作者
Joanna M. Sadowska,Monika Ziminska,Cole Ferreira,Austyn Matheson,Auden Balouch,Jasmine Bogle,Samantha J. Wojda,John Redmond,Ahmed Elkashif,Nicholas Dunne,Helen O. McCarthy,Seth W. Donahue,Fergal J. O’Brien
出处
期刊:Biomaterials
[Elsevier]
日期:2023-11-13
卷期号:303: 122398-122398
被引量:10
标识
DOI:10.1016/j.biomaterials.2023.122398
摘要
Very large bone defects significantly diminish the vascular, blood, and nutrient supply to the injured site, reducing the bone's ability to self-regenerate and complicating treatment. Delivering nanomedicines from biomaterial scaffolds that induce host cells to produce bone-healing proteins is emerging as an appealing solution for treating these challenging defects. In this context, microRNA-26a mimics (miR-26a) are particularly interesting as they target the two most relevant processes in bone regeneration-angiogenesis and osteogenesis. However, the main limitation of microRNAs is their poor stability and issues with cytosolic delivery. Thus, utilising a collagen-nanohydroxyapatite (coll-nHA) scaffold in combination with cell-penetrating peptide (RALA) nanoparticles, we aimed to develop an effective system to deliver miR-26a nanoparticles to regenerate bone defects in vivo. The microRNA-26a complexed RALA nanoparticles, which showed the highest transfection efficiency, were incorporated into collagen-nanohydroxyapatite scaffolds and in vitro assessment demonstrated the miR-26a-activated scaffolds effectively transfected human mesenchymal stem cells (hMSCs) resulting in enhanced production of vascular endothelial growth factor, increased alkaline phosphatase activity, and greater mineralisation. After implantation in critical-sized rat calvarial defects, micro CT and histomorphological analysis revealed that the miR-26a-activated scaffolds improved bone repair in vivo, producing new bone of superior quality, which was highly mineralised and vascularised compared to a miR-free scaffold. This innovative combination of osteogenic collagen-nanohydroxyapatite scaffolds with multifunctional microRNA-26a complexed nanoparticles provides an effective carrier delivering nanoparticles locally with high efficacy and minimal off-target effects and demonstrates the potential of targeting osteogenic-angiogenic coupling using scaffold-based nanomedicine delivery as a new "off-the-shelf" product capable of healing complex bone injuries.
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