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Regulatory effects of stress release from decellularized periosteum on proliferation, migration, and osteogenic differentiation of periosteum-derived cells.
Dong, Gangli; Wang, Jinsong; Chen, Zhongmin; Wang, Fuping; Xia, Bin; Chen, Guobao.
Affiliation
  • Dong G; School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, P. R. China. gbchen@cqut.edu.cn.
  • Wang J; School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, P. R. China. gbchen@cqut.edu.cn.
  • Chen Z; School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, P. R. China. gbchen@cqut.edu.cn.
  • Wang F; School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, P. R. China. gbchen@cqut.edu.cn.
  • Xia B; Engineering Research Center for Waste Oil Recovery Technology and Equipment, Ministry of Education, Chongqing Technology and Business University, Chongqing 400067, P. R. China. xiabin2018@ctbu.edu.cn.
  • Chen G; School of Pharmacy and Bioengineering, Chongqing University of Technology, Chongqing 400054, P. R. China. gbchen@cqut.edu.cn.
Biomater Sci ; 12(13): 3360-3373, 2024 Jun 25.
Article in En | MEDLINE | ID: mdl-38771565
ABSTRACT
Bone injury is often associated with tears in the periosteum and changes in the internal stress microenvironment of the periosteum. In this study, we investigated the biological effects of periosteal prestress release on periosteum-derived cells (PDCs) and the potential mechanisms of endogenous stem cell recruitment. Decellularized periosteum with natural extracellular matrix (ECM) components was obtained by a combination of physical, chemical, and enzymatic decellularization. The decellularized periosteum removed immunogenicity while retaining the natural network structure and composition of the ECM. The Young's modulus has no significant difference between the periosteum before and after decellularization. The extracted PDCs were further composited with the decellularized periosteum and subjected to 20% stress release. It was found that the proliferative capacity of PDCs seeded on decellularized periosteum was significantly enhanced 6 h after stress release of the periosteum. The cell culture supernatant obtained after periosteal prestress release was able to significantly promote the migration ability of PDCs within 24 h. Enzyme-linked immunosorbnent assay (ELISA) experiments showed that the expression of stroma-derived factor-1α (SDF-1α) and vascular endothelial growth factor (VEGF) in the supernatant increased significantly after 3 h and 12 h of stress release, respectively. Furthermore, periosteal stress release promoted the high expression of osteogenic markers osteocalcin (OCN), osteopontin (OPN), and collagen type I of PDCs. The change in stress environment caused by the release of periosteal prestress was sensed by integrin ß1, a mechanoreceptor on the membrane of PDCs, which further stimulated the expression of YAP in the nucleus. These investigations provided a novel method to evaluate the importance of mechanical stimulation in periosteum, which is also of great significance for the design and fabrication of artificial periosteum with mechanical regulation function.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteogenesis / Periosteum / Stress, Mechanical / Cell Differentiation / Cell Movement / Cell Proliferation Limits: Animals / Humans Language: En Journal: Biomater Sci Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Osteogenesis / Periosteum / Stress, Mechanical / Cell Differentiation / Cell Movement / Cell Proliferation Limits: Animals / Humans Language: En Journal: Biomater Sci Year: 2024 Document type: Article
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