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Magnesium malate-modified calcium phosphate bone cement promotes the repair of vertebral bone defects in minipigs via regulating CGRP.

Authors :
Xu, Hailiang
Tian, Fang
Liu, Youjun
Liu, Renfeng
Li, Hui
Gao, Xinlin
Ju, Cheng
Lu, Botao
Wu, Weidong
Wang, Zhiyuan
Zhu, Lei
Hao, Dingjun
Jia, Shuaijun
Source :
Journal of Nanobiotechnology; 6/25/2024, Vol. 22 Issue 1, p1-23, 23p
Publication Year :
2024

Abstract

Active artificial bone substitutes are crucial in bone repair and reconstruction. Calcium phosphate bone cement (CPC) is known for its biocompatibility, degradability, and ability to fill various shaped bone defects. However, its low osteoinductive capacity limits bone regeneration applications. Effectively integrating osteoinductive magnesium ions with CPC remains a challenge. Herein, we developed magnesium malate-modified CPC (MCPC). Incorporating 5% magnesium malate significantly enhances the compressive strength of CPC to (6.18 ± 0.49) MPa, reduces setting time and improves disintegration resistance. In vitro, MCPC steadily releases magnesium ions, promoting the proliferation of MC3T3-E1 cells without causing significant apoptosis, proving its biocompatibility. Molecularly, magnesium malate prompts macrophages to release prostaglandin E2 (PGE2) and synergistically stimulates dorsal root ganglion (DRG) neurons to synthesize and release calcitonin gene-related peptide (CGRP). The CGRP released by DRG neurons enhances the expression of the key osteogenic transcription factor Runt-related transcription factor-2 (RUNX2) in MC3T3-E1 cells, promoting osteogenesis. In vivo experiments using minipig vertebral bone defect model showed MCPC significantly increases the bone volume fraction, bone density, new bone formation, and proportion of mature bone in the defect area compared to CPC. Additionally, MCPC group exhibited significantly higher levels of osteogenesis and angiogenesis markers compared to CPC group, with no inflammation or necrosis observed in the hearts, livers, or kidneys, indicating its good biocompatibility. In conclusion, MCPC participates in the repair of bone defects in the complex post-fracture microenvironment through interactions among macrophages, DRG neurons, and osteoblasts. This demonstrates its significant potential for clinical application in bone defect repair. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
14773155
Volume :
22
Issue :
1
Database :
Complementary Index
Journal :
Journal of Nanobiotechnology
Publication Type :
Academic Journal
Accession number :
178085644
Full Text :
https://doi.org/10.1186/s12951-024-02595-1