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Stem cell-based gene delivery mediated by cationic niosomes for bone regeneration
Noha Attia1, Mohamed Mashal2, Santiago Grijalvo3
1NanoBioCel Group, Laboratory of Pharmaceutics, School of Pharmacy, University of the Basque Country (UPV/EHU), Paseo de la Universidad 7, Vitoria-Gasteiz, Spain; Histology and Cell Biology Department, Faculty of Medicine, University of Alexandria, Alexandria, Egypt.
Gene therapy using niosomes effectively delivered bone morphogenetic protein-7 (BMP-7) to mesenchymal stem cells (MSCs). This approach enhanced bone formation, offering a promising strategy for bone regeneration.
Area of Science:
- Biomaterials Science
- Regenerative Medicine
- Gene Therapy
Background:
- Bone morphogenetic protein-7 (BMP-7) is crucial for bone formation but has a short half-life, limiting its therapeutic use.
- Gene therapy presents a potential solution for sustained BMP-7 delivery to mesenchymal stem cells (MSCs).
Purpose of the Study:
- To develop and characterize niosomes for delivering the BMP-7 gene to D1-MSCs.
- To evaluate the osteogenic differentiation potential of MSCs transfected with the BMP-7 gene via niosomes.
Main Methods:
- Niosomes were formulated using a cationic lipid and polysorbate 80.
- Niosomes were complexed with reporter and BMP-7 plasmids.
- MSCs were transfected, and osteogenic differentiation was assessed via alkaline phosphatase activity and extracellular matrix deposition.
- Endocytic pathway blockers were used to study intracellular uptake.
Main Results:
- Niosomes successfully delivered the BMP-7 gene to MSCs.
- Transfected MSCs exhibited increased proliferation and alkaline phosphatase activity.
- Enhanced extracellular matrix deposition indicated osteoblast-like cell formation.
Conclusions:
- Niosome-mediated BMP-7 gene delivery is effective for inducing osteogenic differentiation in MSCs.
- BMP-7-transfected MSCs serve as a dual tool for gene delivery and bone formation, beneficial for bone regeneration therapies.
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