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Research
Longhao Jin
Yanbian University Hospital
Corresponding Author
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Background
Autologous bone marrow buffy coat transplantation possesses obvious advantages in the therapy of large cartilage defects and osteoarthritis. However, there is no definite research on the specific effective components of bone marrow buffy coat and its mechanism of cartilage regeneration. Moreover, as the crucial cartilage regenerative cell in bone marrow buffy coat, mesenchymal stem cells(MSCs) are difficult to fix onto the damaged cartilage area without damaging the subchondral bone. We assessed the effect of using hyaluronic acid(HA) as a liquid scaffold mixed with autologous bone marrow buffy coat to fix cartilage defect.
Methods and Materials
We extracted the bone marrow from the anterior superior iliac crest of the white New Zealand rabbit, centrifuged to obtain a buffy coat, and analyzed the components of buffy coat by ELISA. Buffy coat+HA group, MSC+HA group, MSC+TGF-β+HA group were cultured in vitro and observed by staining. In addition, we made damage to the femoral condyle of rabbits, and divided them into groups: HA group, buffy coat group, buffy coat with HA group. Each group was assessed for cartilage regeneration by visual observation, histological and immunohistochemical analysis at 4 weeks and 8 weeks, and biochemical analysis at 8 weeks postoperatively. One-way ANOVA and LSD were used for statistic analysis.
Results
Buffy coat have a variety of growth factors, inflammatory factors and anti-inflammatory factors that stimulate the MSCs’ regeneration. Buffy coat can differentiate into cartilage without TGF-β stimulation in vitro. The cartilage regeneration ability of buffy coat and buffy coat+HA is strong, and the combination of buffy coat and liquid scaffold HA can make cartilage formation ability more stable in vivo.
Conclusion
MSC, multiple growth factors and cytokines in buffy coat synergistically promote cartilage regeneration. Liquid scaffold HA enhances the effect of buffy coat on cartilage attachment and regeneration of cartilage defects.
Keywords
Cartilage Repair, Buffy Coat, Mesenchymal Stem Cells, Osteoarthritis
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A new preprint design is coming!
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This is a preprint, a preliminary version of a manuscript that has not completed peer review at a journal. Research Square does not conduct peer review prior to posting preprints. The posting of a preprint on this server should not be interpreted as an endorsement of its validity or suitability for dissemination as established information or for guiding clinical practice.
Research
Longhao Jin
Yanbian University Hospital
Corresponding Author
Badges
Prescreen
This manuscript passed our Prescreen assessment
Complete author information
Appropriate declaration statements
Potential risks to human health
Prescreen
History
CURRENT STATUS: Posted
The most recent version of this article is available here.
No community comments so far
Metrics
Comments: 0
PDF Downloads: ...
HTML Views: ...
Subject Areas
Stem Cell & Developmental Cell Biology
License:
This work is licensed under a CC BY 4.0 License. Read Full License
The most recent version of this article is available here.
Background
Autologous bone marrow buffy coat transplantation possesses obvious advantages in the therapy of large cartilage defects and osteoarthritis. However, there is no definite research on the specific effective components of bone marrow buffy coat and its mechanism of cartilage regeneration. Moreover, as the crucial cartilage regenerative cell in bone marrow buffy coat, mesenchymal stem cells(MSCs) are difficult to fix onto the damaged cartilage area without damaging the subchondral bone. We assessed the effect of using hyaluronic acid(HA) as a liquid scaffold mixed with autologous bone marrow buffy coat to fix cartilage defect.
Methods and Materials
We extracted the bone marrow from the anterior superior iliac crest of the white New Zealand rabbit, centrifuged to obtain a buffy coat, and analyzed the components of buffy coat by ELISA. Buffy coat+HA group, MSC+HA group, MSC+TGF-β+HA group were cultured in vitro and observed by staining. In addition, we made damage to the femoral condyle of rabbits, and divided them into groups: HA group, buffy coat group, buffy coat with HA group. Each group was assessed for cartilage regeneration by visual observation, histological and immunohistochemical analysis at 4 weeks and 8 weeks, and biochemical analysis at 8 weeks postoperatively. One-way ANOVA and LSD were used for statistic analysis.
Results
Buffy coat have a variety of growth factors, inflammatory factors and anti-inflammatory factors that stimulate the MSCs’ regeneration. Buffy coat can differentiate into cartilage without TGF-β stimulation in vitro. The cartilage regeneration ability of buffy coat and buffy coat+HA is strong, and the combination of buffy coat and liquid scaffold HA can make cartilage formation ability more stable in vivo.
Conclusion
MSC, multiple growth factors and cytokines in buffy coat synergistically promote cartilage regeneration. Liquid scaffold HA enhances the effect of buffy coat on cartilage attachment and regeneration of cartilage defects.
Figure 1
Figure 2
Figure 3
Figure 4
Figure 5
Figure 6
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