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转染肌腱形成蛋白基因的骨髓间充质干细胞改善大鼠肩袖愈合。

Bone marrow-derived mesenchymal stem cells transduced with scleraxis improve rotator cuff healing in a rat model.

机构信息

Hospital for Special Surgery, New York, NY 10021, USA.

出版信息

Am J Sports Med. 2011 Jun;39(6):1282-9. doi: 10.1177/0363546510395485. Epub 2011 Feb 18.

Abstract

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.

摘要

背景

肩袖修复后通过疤痕组织界面愈合,这使其容易发生失败。 Scleraxis(Scx)是一种基本的螺旋环 - 螺旋转录因子,被认为在胚胎发生期间指导肌腱发育。本研究的目的是确定骨髓间充质干细胞(MSCs)转导腺病毒介导的 Scleraxis(Ad-Scx)是否可以改善大鼠肩袖修复模型中腱骨插入部位的再生。

假设

转导 Scx 的骨髓细胞可改善愈合腱骨界面的结构,并导致腱附着强度增加。

研究设计

对照实验室研究。

方法

60 只 Lewis 大鼠接受单侧肩袖上棘肌腱分离和修复。 30 只动物接受纤维蛋白胶载体中的 MSC,30 只接受 Ad-Scx 转导的 MSC。动物在 2 周和 4 周时处死,并评估插入处纤维软骨和胶原纤维组织的存在。生物力学测试用于确定修复组织的结构和材料特性。采用 Wilcoxon 秩和检验进行统计分析,显著性水平为 P =.05。

结果

在 2 周时,Scx 组和 MSC 组在组织学表现方面没有差异。 然而,Scx 组的最终失效应力(2.6 ± 0.9 与 1.7 ± 0.3 MPa;P =.03)和刚度(8.4 ± 2.9 与 5.0 ± 1.9 N/mm;P =.01)均高于 MSC 组。 4 周时,Scx 组的纤维软骨更多(728.7 ± 50.4 与 342.6 ± 217.0 mm(2);P =.04),最终失效载荷更高(26.7 ± 4.6 与 20.8 ± 4.4 N;P =.01),最终失效应力更高(4.7 ± 1.3 与 3.5 ± 1.0 MPa;P <.04),刚度值更高(15.3 ± 3.4 与 9.3 ± 2.2 N/mm;P <.001)与 MSC 组相比。

结论

用 Scx 基因修饰的间充质干细胞可以在早期时间点增强肩袖的愈合。

临床相关性

用 Scx 转导的 MSC 对急性损伤的肩袖进行生物学增强可能会改善肩袖肌腱愈合并降低再撕裂的发生率。 然而,需要进一步的研究来确定在更大的模型中这种方法是否仍然安全有效。

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