Bone Regeneration Potential of Stem Cells Derived from Periodontal Ligament or Gingival Tissue Sources Encapsulated in RGD-Modified Alginate Scaffold

• Published in: Tissue engineering. Part A Vol. 20; no. 3-4; pp. 611 - 621
• Main Authors: Moshaverinia, Alireza, Chen, Chider, Xu, Xingtian, Akiyama, Kentaro, Ansari, Sahar, Zadeh, Homayoun H., Shi, Songtao
• Format: Journal Article
• Language: English
• Published: United States Mary Ann Liebert, Inc 01.02.2014
• Subjects: Adolescent; Adult; Alginates - pharmacology; Animals; Bone Regeneration - drug effects; Bones; Cell Differentiation - drug effects; Cell Lineage - drug effects; Cell Survival - drug effects; Cells, Immobilized - cytology; Cells, Immobilized - drug effects; Cells, Immobilized - metabolism; Colony-Forming Units Assay; Gingiva - cytology; Glucuronic Acid - pharmacology; Hexuronic Acids - pharmacology; Humans; Male; Mesenchymal Stem Cell Transplantation; Mesenchymal Stromal Cells - cytology; Mesenchymal Stromal Cells - drug effects; Mesenchymal Stromal Cells - metabolism; Mice; Mice, Nude; Microfluidics; Models, Animal; Oligopeptides - pharmacology; Original; Original Articles; Osteogenesis - drug effects; Periodontal Ligament - cytology; Skull - pathology; Stem cells; Tissue engineering; Tissue Scaffolds - chemistry; Transcription Factors - metabolism; Young Adult
• ISSN: 1937-3341; 1937-335X
• DOI: 10.1089/ten.tea.2013.0229

Mesenchymal stem cells (MSCs) provide an advantageous alternative therapeutic option for bone regeneration in comparison to current treatment modalities. However, delivering MSCs to the defect site while maintaining a high MSC survival rate is still a critical challenge in MSC-mediated bone regeneration. Here, we tested the bone regeneration capacity of periodontal ligament stem cells (PDLSCs) and gingival mesenchymal stem cells (GMSCs) encapsulated in a novel RGD- (arginine-glycine-aspartic acid tripeptide) coupled alginate microencapsulation system in vitro and in vivo . Five-millimeter-diameter critical-size calvarial defects were created in immunocompromised mice and PDLSCs and GMSCs encapsulated in RGD-modified alginate microspheres were transplanted into the defect sites. New bone formation was assessed using microcomputed tomography and histological analyses 8 weeks after transplantation. Results confirmed that our microencapsulation system significantly enhanced MSC viability and osteogenic differentiation in vitro compared with non-RGD-containing alginate hydrogel microspheres with larger diameters. Results confirmed that PDLSCs were able to repair the calvarial defects by promoting the formation of mineralized tissue, while GMSCs showed significantly lower osteogenic differentiation capability. Further, results revealed that RGD-coupled alginate scaffold facilitated the differentiation of oral MSCs toward an osteoblast lineage in vitro and in vivo , as assessed by expression of osteogenic markers Runx2, ALP, and osteocalcin. In conclusion, these results for the first time demonstrated that MSCs derived from orofacial tissue encapsulated in RGD-modified alginate scaffold show promise for craniofacial bone regeneration. This treatment modality has many potential dental and orthopedic applications.