Development of miR-26a-activated scaffold to promote healing of critical-sized bone defects through angiogenic and osteogenic mechanisms
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.
Funding
National Science Foundation (Award #1854387)
Science Foundation Ireland under the US-Ireland Research and Development Partnership (17/ US/3437; Ireland)
European Research Council under the European Community's Horizon 2020 research and innovation programme under the ERC Advanced Grant agreement n° 788753 (ReCaP)
Marie Skłodowska-Curie Individual Fellowships from the European Commission through the H2020 project GAMBBa (Project ID: 892389)
ON Foundation, Switzerland
US-Ireland Grant 130
History
Comments
The original article is available at https://www.sciencedirect.com/Published Citation
Sadowska JM, et al. Development of miR-26a-activated scaffold to promote healing of critical-sized bone defects through angiogenic and osteogenic mechanisms. Biomaterials. 2023;303:122398.Publication Date
13 November 2023PubMed ID
37979514Department/Unit
- Tissue Engineering Research Group (TERG)
- Anatomy and Regenerative Medicine
- Amber (Advanced Material & Bioengineering Research) Centre
Publisher
Elsevier B.V.,Version
- Published Version (Version of Record)