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首页> 外文期刊>American Journal of Sports Medicine >Bone marrow-derived mesenchymal stem cells transduced with scleraxis improve rotator cuff healing in a rat model.
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Bone marrow-derived mesenchymal stem cells transduced with scleraxis improve rotator cuff healing in a rat model.

机译:硬化诱导的骨髓源间充质干细胞可改善大鼠模型中肩袖的愈合。

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BACKGROUND: Rotator cuffs heal through a scar tissue interface after repair that makes them prone to failure. Scleraxis (Scx) is a basic helix-loop-helix transcription factor that is thought to direct tendon development during embryogenesis. The purpose of this study was to determine if the application of mesenchymal stem cells (MSCs) transduced with adenoviral-mediated scleraxis (Ad-Scx) could improve regeneration of the tendon-bone insertion site in a rat rotator cuff repair model. HYPOTHESIS: Bone marrow-derived cells transduced with Scx would improve the structure of the healing tendon-bone interface and result in increased tendon attachment strength. STUDY DESIGN: Controlled laboratory study. METHODS: Sixty Lewis rats underwent unilateral detachment and repair of the supraspinatus tendon. Thirty animals received MSCs in a fibrin glue carrier, and 30 received Ad-Scx-transduced MSCs. Animals were sacrificed at 2 weeks and 4 weeks and evaluated for the presence of fibrocartilage and collagen fiber organization at the insertion. Biomechanical testing was performed to determine the structural and material properties of the repaired tissue. Statistical analysis was performed with a Wilcoxon rank sum test with significance set at P = .05. RESULTS: There were no differences between the Scx and MSC groups in terms of histologic appearance at 2 weeks. However, the Scx group had higher ultimate stress-to-failure (2.6 +/- 0.9 vs 1.7 +/- 0.3 MPa; P = .03) and stiffness (8.4 +/- 2.9 vs 5.0 +/- 1.9 N/mm; P = .01) compared with the MSC group. At 4 weeks, the Scx group had more fibrocartilage (728.7 +/- 50.4 vs 342.6 +/- 217.0 mm(2); P = .04), higher ultimate load to failure (26.7 +/- 4.6 vs 20.8 +/- 4.4 N; P = .01), higher ultimate stress to failure (4.7 +/- 1.3 vs 3.5 +/- 1.0 MPa; P < .04), and higher stiffness values (15.3 +/- 3.4 vs 9.3 +/- 2.2 N/mm; P < .001) as compared with the MSC group. CONCLUSION: Mesenchymal stem cells genetically modified with Scx can augment rotator cuff healing at early time points. CLINICAL RELEVANCE: Biologic augmentation of acutely injured rotator cuffs with Scx-transduced MSCs may improve rotator cuff tendon healing and reduce the incidence of re-tears. However, further studies are needed to determine if this remains safe and effective in larger models.
机译:背景:修复后的肩袖可通过疤痕组织界面愈合,这使其易于失效。巩膜硬化(Scx)是一种基本的螺旋-环-螺旋转录因子,被认为可指导胚胎发生过程中肌腱的发育。这项研究的目的是确定应用腺病毒介导的巩膜硬化(Ad-Scx)转导的间充质干细胞(MSC)是否可以改善大鼠肩袖修复模型中腱-骨插入位点的再生。假设:用Scx转导的骨髓来源的细胞将改善愈合的腱-骨界面的结构,并导致增强的腱附着强度。研究设计:受控实验室研究。方法:60只Lewis大鼠单侧脱离并修复了棘上肌腱。 30只动物在纤维蛋白胶载体中接受了MSC,而30只动物接受了Ad-Scx转导的MSC。在第2周和第4周处死动物,并在插入时评估其纤维软骨和胶原纤维组织的存在。进行生物力学测试以确定修复组织的结构和材料特性。用Wilcoxon秩和检验进行统计学分析,显着性设置为P = .05。结果:2周时,Scx组和MSC组在组织学外观上没有差异。然而,Scx组的最终破坏应力更高(2.6 +/- 0.9 vs 1.7 +/- 0.3 MPa; P = .03)和刚度(8.4 +/- 2.9 vs 5.0 +/- 1.9 N / mm; P = 0.01)与MSC组相比。在第4周时,Scx组的纤维软骨更多(728.7 +/- 50.4 vs 342.6 +/- 217.0 mm(2); P = .04),更高的最终衰竭负荷(26.7 +/- 4.6 vs 20.8 +/- 4.4 N; P = .01),更高的破坏极限应力(4.7 +/- 1.3 vs 3.5 +/- 1.0 MPa; P <.04),更高的刚度值(15.3 +/- 3.4 vs 9.3 +/- 2.2 N / mm; P <.001)与MSC组相比。结论:经Scx基因修饰的间充质干细胞可在早期时间促进肩袖愈合。临床相关性:用Scx转导的MSCs对急性受伤的肩袖进行生物增强可能会改善肩袖腱的愈合,并减少再次撕裂的发生。但是,需要进行进一步的研究以确定在较大的模型中这是否仍然安全有效。

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