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Therapeutic potential of epiphyseal growth plate cells for bone regeneration in an osteoporosis model.
Baek, Inho; Bello, Alvin Bacero; Jeon, Jieun; Arai, Yoshie; Cha, Byung-Hyun; Kim, Byoung Ju; Lee, Soo-Hong.
Afiliación
  • Baek I; Department of Medical Biotechnology, Dongguk University, Goyang, Gyeonggi, Republic of Korea.
  • Bello AB; Department of Medical Biotechnology, Dongguk University, Goyang, Gyeonggi, Republic of Korea.
  • Jeon J; Department of Medical Biotechnology, Dongguk University, Goyang, Gyeonggi, Republic of Korea.
  • Arai Y; Department of Medical Biotechnology, Dongguk University, Goyang, Gyeonggi, Republic of Korea.
  • Cha BH; Division of Biomedical Convergence, College of Biomedical Science, Kangwon National University, Chuncheon, Republic of Korea.
  • Kim BJ; ATEMs, Seoul, Republic of Korea.
  • Lee SH; Department of Medical Biotechnology, Dongguk University, Goyang, Gyeonggi, Republic of Korea.
J Tissue Eng ; 13: 20417314221116754, 2022.
Article en En | MEDLINE | ID: mdl-35983547
ABSTRACT
Bone growth occurs in the epiphyseal growth plate (EGP) and epiphyseal growth plate cells (EGPCs) exist in EGP. EGPCs, including skeletal stem cells (SSCs), are cells that induce bone growth and development through endochondral ossification. Recently, the superiority of bone regeneration through endochondral ossification has been reported. Our study compared EGPCs with bone marrow-derived mesenchymal stem cells (BM-MSCs) and suggested the therapeutic potential of new bone regeneration. In this study, we analyzed the characteristics between EGPCs and BM-MSCs based on morphological characteristics and molecular profiles. EGPCs expressed chondrogenic and osteogenic markers higher than BM-MSCs. Additionally, in co-culture with BM-MSCs, EGPCs induced an increase in chondrogenic, osteogenic, and hypertrophic markers of BM-MSCs. Finally, EGPCs induced higher bone regeneration than BM-MSCs in the osteoporosis model. Overall, we suggest the possibility of EGPCs as cell therapy for effective bone regeneration.
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Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Tissue Eng Año: 2022 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: J Tissue Eng Año: 2022 Tipo del documento: Article