scholarly journals Bone Mesenchymal Stem Cells Contribute to Ligament Regeneration and Graft–Bone Healing after Anterior Cruciate Ligament Reconstruction with Silk–Collagen Scaffold

2021 ◽  
Vol 2021 ◽  
pp. 1-11
Author(s):  
Fanggang Bi ◽  
Yangdi Chen ◽  
Junqi Liu ◽  
Wenhao Hu ◽  
Ke Tian

Anterior cruciate ligament (ACL) reconstruction was realized using a combination of bone mesenchymal stem cells (BMSCs) and silk–collagen scaffold, and an in vivo evaluation of this combination was performed. By combining type I collagen and degummed silk fibroin mesh, silk–collagen scaffolds were prepared to simulate ligament components. BMSCs isolated from bone marrow of rabbits were cultured for a homogenous population and seeded on the silk–collagen scaffold. In the scaffold and BMSC (S/C) group, scaffolds were seeded with BMSCs for 72 h and then rolled and used to replace the ACL in 20 rabbits. In the scaffold (S) group, scaffolds immersed only in culture medium for 72 h were used for ACL reconstruction. Specimens were collected at 4 and 16 weeks postoperatively to assess ligament regeneration and bone integration. HE and immunohistochemical staining (IHC) were performed to assess ligament regeneration in the knee cavity. To assess bone integration at the graft–bone interface, HE, Russell–Movat staining, micro-CT, and biomechanical tests were performed. After 4 weeks, vigorous cell proliferation was observed in the core part of the scaffold in the S/C group, and a quantity of fibroblast-like cells and extracellular matrix (ECM) was observed in the center part of the graft at 16 weeks after surgery. At 4 and 16 weeks postoperatively, the tenascin-C expression in the S/C group was considerably higher than that in the S group (4 w, p < 0.01 ; 16 w, p < 0.01 ). Furthermore, bone integration was better in the S/C group than in the S group, with histological observation of trabecular bone growth into the graft and more mineralized tissue formation detected by micro-CT (4 w, bone volume fraction (BV/TV), p = 0.0169 , bone mineral density (BMD), p = 0.0001 ; 16 w, BV/TV, p = 0.1233 , BMD, p = 0.0494 ). These results indicate that BMSCs promote ligament regeneration in the knee cavity and bone integration at the graft–bone interface. Silk–collagen scaffolds and BMSCs will likely be combined for clinical practice in the future.

Biomaterials ◽  
2008 ◽  
Vol 29 (23) ◽  
pp. 3324-3337 ◽  
Author(s):  
Hongbin Fan ◽  
Haifeng Liu ◽  
Eugene J.W. Wong ◽  
Siew L. Toh ◽  
James C.H. Goh

2012 ◽  
Vol 18 (23-24) ◽  
pp. 2549-2558 ◽  
Author(s):  
Jose A. Canseco ◽  
Koji Kojima ◽  
Ashley R. Penvose ◽  
Jason D. Ross ◽  
Haruko Obokata ◽  
...  

2015 ◽  
Vol 40 (7) ◽  
pp. 1523-1530 ◽  
Author(s):  
Weili Fu ◽  
Qi Li ◽  
Xin Tang ◽  
Gang Chen ◽  
Chenghao Zhang ◽  
...  

2020 ◽  
Vol 56 (1) ◽  
pp. 41
Author(s):  
Dwikora Novembri Utomo ◽  
Ferdiansyah Mahyudin ◽  
Arif Zulkarnain ◽  
Purwati Purwati ◽  
Rossy Setyawati

Graft tunnel healing is important for the successful reconstruction of the anterior cruciate ligament by using the hamstring tendon autograft. There are studies that intra graft tunnel Bone Marrow Mesenchymal stem cells (BMSCs) or intra graft tunnel Vascular endothelial growth factor (VEGF) accelerated graft tunnel healing. This study aimed to investigate the effect of using BMSCs+VEGF injected intra-articular on graft tunnel healing. We reconstructed the anterior cruciate ligament (ACL) of 12 rabbits using an autograft hamstring tendon with and without intra-articular BMSCs+VEGF. Histological evaluation was done at 3 and 6 weeks after ACL reconstruction. On the surface between the graft and the bone tunnel obtained collagen fiber thickness or Sharpey fiber is significantly more than the control group (p< 0.05) in the evaluation of 3 weeks and 6 weeks either side of the tibia and the femur. To evaluate the progression of the treatment, treatment group and control group gained progression had significantly when compared to 3 weeks and 6 weeks. It can be concluded that intra-articular injection of VEGF+BMSCs can accelerate the integration of the graft tunnel from histology evaluation on 3 and 6 weeks.


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