Application of Tendon-Derived Stem Cell Sheet for the Promotion of Graft Healing in Anterior Cruciate Ligament Reconstruction

医学 前交叉韧带重建术 CTGF公司 结缔组织 抗坏血酸 前交叉韧带 肌腱 骨愈合 病理 干细胞 解剖 外科 生长因子 化学 内科学 生物 细胞生物学 受体 食品科学
作者
Pauline Po Yee Lui,On Tik Wong,Yuk Wa Lee
出处
期刊:American Journal of Sports Medicine [SAGE Publishing]
卷期号:42 (3): 681-689 被引量:116
标识
DOI:10.1177/0363546513517539
摘要

Background: Both osteointegration and remodeling of graft midsubstance (collectively called graft healing) are slow processes after anterior cruciate ligament (ACL) reconstruction. Tendon-derived stem cells (TDSCs) form a cell sheet after treatment with connective tissue growth factor (CTGF) and ascorbic acid, which exhibits higher tenogenic and maintains high chondro-osteogenic gene expression of TDSCs. No external scaffold is required for cell delivery. Hypothesis: Wrapping the TDSC sheet around the ACL graft would promote early graft healing in a rat model. Study Design: Controlled laboratory study. Methods: Green fluorescent protein (GFP) rat TDSCs were treated with connective tissue growth factor and ascorbic acid to promote cell sheet formation. Rats undergoing unilateral ACL reconstruction were divided into a control group and a TDSC group. The tendon graft was wrapped with the GFP-TDSC sheet before graft insertion in the TDSC group. At weeks 2, 6, and 12 after reconstruction, the samples were harvested for computed tomography imaging and histologic or biomechanical testing. The fate of the transplanted cell sheet was examined by immunohistochemical staining of GFP. Results: There were significantly higher tunnel bone mineral density (BMD) (42.3% increase, P = .047) and bone volume/total volume (BV/TV) (625% increase, P = .009) at the metaphyseal region of the tibial tunnel at week 2 and at the femoral tunnel at week 6 (BMD: 30.8% increase, P = .014; BV/TV: 100% increase, P = .014) in the TDSC group compared with the control group. Only the TDSC group showed a time-dependent increase in tunnel BMD (overall P = .038) and BV/TV (overall P = .015) at the epiphyseal region of the tibial tunnel. Semiquantitative image analysis showed better graft osteointegration and higher intra-articular graft integrity with lower cellularity and vascularity, better cell alignment, and higher collagen birefringence in the TDSC group. The ultimate load at week 2 (52.5% increase, P = .027) and stiffness at week 6 (62% increase, P = .008) were significantly higher in the TDSC group. Cells positive for GFP were observed in all samples in the TDSC group at week 2 but became reduced with time after reconstruction. Conclusion: The TDSC sheet improved early graft healing after ACL reconstruction in the rat model. Clinical Relevance: The TDSC sheet could potentially be used for the promotion of graft healing in ACL reconstruction.
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