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Efficacy of Bone Regeneration Cell Therapy Using Mesenchymal Stem Cells Originating from Embryonic Stem Cells in Animal Models; Bone Defects and Osteomyelitis

Authors
Park, Jin-HoBae, Han-SolKim, IngeunJung, JiwoonRoh, YoonhoLee, DongbinHwang, Tae SungLee, Hee-ChunByun, June-Ho
Issue Date
Jan-2025
Publisher
한국조직공학과 재생의학회
Keywords
Bone regeneration; Cell therapy; Mesenchymal stem cell; Fibrinization; Osteomyelitis model
Citation
Tissue Engineering and Regenerative Medicine, v.22, no.1, pp 145 - 157
Pages
13
Indexed
SCIE
SCOPUS
KCI
Journal Title
Tissue Engineering and Regenerative Medicine
Volume
22
Number
1
Start Page
145
End Page
157
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/75008
DOI
10.1007/s13770-024-00683-9
ISSN
1738-2696
2212-5469
Abstract
BACKGROUND:Bone defects are commonly encountered due to accidents, diseases, or aging, and the demand for effective bone regeneration, particularly for dental implants, is increasing in our aging society. Mesenchymal stem cells (MSCs) are promising candidates for regenerative therapies; however, obtaining sufficient quantities of these cells for clinical applications remains challenging. DW-MSCs, derived from embryonic stem cells and developed by Daewoong Pharmaceutical, exhibit a robust proliferative capacity even after extensive culture.METHODS:This study explores the therapeutic potential of DW-MSCs in various animal models of bone defects. DW-MSCs were expanded for over 13 passages for in vivo use in rat and canine models of bone defects and osteomyelitis. The research focused on the in vivo osteogenic differentiation of DW-MSCs, the establishment of a fibrin-based system for bone regeneration, the assessment of bone repair following treatment in animal models, and comparisons with commercially available bone grafts.RESULTS:Results showed that DW-MSCs exhibited superior osteogenic differentiation compared to other materials, and the fibrinization process not only preserved but enhanced their proliferation and differentiation capabilities through a 3D culture effect. In both bone defect models, DW-MSCs facilitated significant bone regeneration, reduced inflammatory responses in osteomyelitis, and achieved effective bone healing. The therapeutic outcomes of DW-MSCs were comparable to those of commercial bone grafts but demonstrated qualitatively superior bone tissue restructuring.CONCLUSION:Our findings suggest that DW-MSCs offer a promising approach for bone regeneration therapies due to their high efficacy and anti-inflammatory properties.
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