Absence of bone sialoprotein (BSP) impairs cortical defect repair in mouse long bone

Bone ◽  
2009 ◽  
Vol 45 (5) ◽  
pp. 853-861 ◽  
Author(s):  
Luc Malaval ◽  
Laurent Monfoulet ◽  
Thierry Fabre ◽  
Laurent Pothuaud ◽  
Reine Bareille ◽  
...  
2019 ◽  
Author(s):  
Lin Zhao ◽  
Jia-Jia Yu ◽  
Cangyu Zhang ◽  
Xiuhui Wang

Abstract Background As an alternative of bone grafts for defect repair, tissue engineering is much promising for clinical application. In previous studies, we have succeeded in repair of long bone defect with homemade tissue-engineered periosteum (TEP), of which is fabraicated by incorporating osteogenically induced mesenchymal stem cells (MSCs) of rabbits with a scaffold of small intestinal submucosa (SIS).Methods In this study, we are aimed to discuss the feasibility of allogenic irregular bone defect repair with the TEP. Thirty-six rabbits whose scapulas were subtotally resected to establish large irregular bone defects model in allogenic rabbits. The defects were treat respectively with TEP (Group 1, n=12), allogenic deproteinized bone (DPB) (Group 2, n=12) and hybrid of TEP and DPB (Group 3, n=12). At 4, 8, and 12 weeks after surgery, the rabbits were sacrificed, and the implants were harvested. X-ray radiographic and histological examinations were performed.ResultsThe findings suggested that the radiographic score in TEP-DPB hybrided implantation (Group 3) was higher than TEP or DPB grafting only (p<0.05).But that was inconsistent with histological findings, which Group1 appeared to possess significantly higher bone formation than Group 2 (p<0.05) and Group3 has higher new bone volume than that of Group 2 (p<0.05).Conclusion We conclude that TEP is a promising alternative in repair of large irregular bone defect.DPB served as a 3D scaffold in combining TEP could provide mechanical support and shaping guide, but hinder new bone formation via TEP approach due to retard degradation.


2017 ◽  
Author(s):  
Chao Liu ◽  
Robert Carrera ◽  
Vittoria Flamini ◽  
Lena Kenny ◽  
Pamela Cabahug-Zuckerman ◽  
...  

AbstractMechanical loading is an important aspect of post-surgical care. The timing of load application relative to the injury event is thought to differentially regulate repair depending on the stage of healing. Here, we show using a novel mechanobiological model of cortical defect repair that daily loading (5 N peak load, 2 Hz, 60 cycles, 4 consecutive days) during hematoma consolidation and inflammation disrupts the injury site and activates cartilage formation on the periosteal surface adjacent to the defect. We also show that daily loading during the matrix deposition phase enhances both bone and cartilage formation at the defect site, while loading during the remodeling phase results in an enlarged woven bone regenerate. All loading regimens resulted in abundant cellular proliferation within the regenerate and at the periosteal surface and fibrous tissue formation directly above the defect. Stress was concentrated at the edges of the defect during exogenous loading, and finite element (FE)-modeled longitudinal strain (εzz) values along the anterior and posterior borders of the defect (~2200 με) were an order of magnitude larger than strain values on the proximal and distal borders (~50-100 με). These findings demonstrate that all phases of cortical defect healing are sensitive to physical stimulation. In addition, the proposed novel mechanobiological model offers several advantages including its technical simplicity and its well-characterized and spatially confined repair program, making effects of physical and biological interventions more easily assessed.


2020 ◽  
Vol 17 (5) ◽  
pp. 717-727
Author(s):  
Lin Zhao ◽  
Junli Zhao ◽  
Jia-Jia Yu ◽  
Cangyu Zhang

Abstract Background: In previous studies, we succeeded in repairing a long bone defect with tissue-engineered periosteum (TEP), fabricated by incorporating rabbit mesenchymal stem cells with small intestinal submucosa. In this study, we investigated the feasibility of allogeneic irregular bone defect repair using TEP. Methods: We performed a subtotal resection of the scapula in 36 rabbits to establish a large irregular bone defect model. The rabbits were then randomly divided into three groups (n = 12 per group) and the defects were treated with TEP (Group 1), allogeneic deproteinized bone (DPB) (Group 2) or a hybrid of TEP and DPB (Group 3). At 4, 8, and 12 weeks after surgery, the rabbits were sacrificed, and the implants were harvested. X-ray radiographic and histological examinations were performed to detect bone healing. Ink-formaldehyde perfusion was introduced to qualitatively analyze vascularization in TEP engineered new bone. Results: The repair of scapular defects was diverse in all groups, shown by radiographic and histological tests. The radiographic scores in Group 1 and Group 3 were significantly higher than Group 2 at 8 and 12 weeks (p < 0.05). Histological scores further proved that Group 1 had significantly greater new bone formation compared to Group 3 (p < 0.05), while Group 2 had the lowest osteogenesis at all time-points (p < 0.001). Ink-formaldehyde perfusion revealed aboundant microvessels in TEP engineered new bone. Conclusion: We conclude that TEP is promising for the repair of large irregular bone defects. As a 3D scaffold, DPB could provide mechanical support and a shaping guide when combined with TEP. TEP engineered new bone has aboundant microvessels.


Bone ◽  
2010 ◽  
Vol 46 (2) ◽  
pp. 447-452 ◽  
Author(s):  
Laurent Monfoulet ◽  
Luc Malaval ◽  
Jane E. Aubin ◽  
Susan R. Rittling ◽  
Alain P. Gadeau ◽  
...  

2011 ◽  
Vol 17 (5-6) ◽  
pp. 691-701 ◽  
Author(s):  
Liang Feng ◽  
Derek J. Milner ◽  
Chunguang Xia ◽  
Holly L.D. Nye ◽  
Patrick Redwood ◽  
...  

2018 ◽  
Vol 172 ◽  
pp. 690-698 ◽  
Author(s):  
Govindaraj Perumal ◽  
Boopalan Ramasamy ◽  
Maya Nandkumar A ◽  
Mukesh Doble

Bone Research ◽  
2022 ◽  
Vol 10 (1) ◽  
Author(s):  
Kai Dai ◽  
Shunshu Deng ◽  
Yuanman Yu ◽  
Fuwei Zhu ◽  
Jing Wang ◽  
...  

AbstractThe periosteum, a highly vascularized thin tissue, has excellent osteogenic and bone regenerative abilities. The generation of periosteum-mimicking tissue has become a novel strategy for bone defect repair and regeneration, especially in critical-sized bone defects caused by trauma and bone tumor resection. Here, we utilized a bone morphogenetic protein-2 (BMP-2)-loaded scaffold to create periosteum-like tissue (PT) in vivo, mimicking the mesenchymal condensation during native long bone development. We found that BMP-2-induced endochondral ossification plays an indispensable role in the construction of PTs. Moreover, we confirmed that BMP-2-induced PTs exhibit a similar architecture to the periosteum and harbor abundant functional periosteum-like tissue-derived cells (PTDCs), blood vessels, and osteochondral progenitor cells. Interestingly, we found that the addition of chondroitin sulfate (CS), an essential component of the extracellular matrix (ECM), could further increase the abundance and enhance the function of recruited PTDCs from the PTs and finally increase the regenerative capacity of the PTs in autologous transplantation assays, even in old mice. This novel biomimetic strategy for generating PT through in vivo endochondral ossification deserves further clinical translation.


PLoS ONE ◽  
2014 ◽  
Vol 9 (5) ◽  
pp. e95144 ◽  
Author(s):  
Wafa Bouleftour ◽  
Maya Boudiffa ◽  
Ndeye Marième Wade-Gueye ◽  
Guénaëlle Bouët ◽  
Marco Cardelli ◽  
...  

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