Development of miR-26a-activated scaffold to promote healing of critical-sized bone defects through angiogenic and osteogenic mechanisms

被引:10
|
作者
Sadowska, Joanna M. [1 ]
Ziminska, Monika [2 ]
Ferreira, Cole [3 ]
Matheson, Austyn [1 ]
Balouch, Auden [3 ]
Bogle, Jasmine [3 ]
Wojda, Samantha [3 ]
Redmond, John [4 ,5 ]
Elkashif, Ahmed [2 ]
Dunne, Nicholas [2 ,4 ,5 ,6 ,7 ,8 ]
Mccarthy, Helen O. [2 ]
Donahue, Seth [3 ]
O'Brien, Fergal J. [1 ,3 ,6 ]
机构
[1] Univ Med & Hlth Sci, Dept Anat & Regenerat Med, Tissue Engn Res Grp, Royal Coll Surg Ireland RCSI, Dublin, Ireland
[2] Queens Univ Belfast, Sch Pharm, Belfast, North Ireland
[3] Univ Massachusetts, Dept Biomed Engn, Amherst, MA USA
[4] RCSI, Adv Mat & Bioengn Res Ctr AMBER, Dublin, Ireland
[5] TCD, Dublin, Ireland
[6] Dublin City Univ, Adv Mfg Res Ctr I Form, Sch Mech & Mfg Engn, Dublin, Ireland
[7] Trinity Coll Dublin TCD, Trinity Ctr Biomed Engn, Dublin, Ireland
[8] Dublin City Univ, Sch Mech & Mfg Engn, Dublin, Ireland
基金
爱尔兰科学基金会; 欧洲研究理事会; 美国国家科学基金会;
关键词
MESENCHYMAL STEM-CELLS; GROWTH-FACTOR DELIVERY; DIFFERENT HYDROXYAPATITE; CONTROLLED-RELEASE; DIFFERENTIATION; REGENERATION; GENE; NANOPARTICLE; MODULATE; MIR-26A;
D O I
10.1016/j.biomaterials.2023.122398
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
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 effec-tively 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.
引用
收藏
页数:14
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