BG Trauma Clinic Tübingen, University Hospital Tübingen, Schnarrenbergstr. 95, 72076 Tübingen, Germany. E-mail address for T.M. Kraus:
Departments of Sports Orthopaedics (G.W., L.L., S.B., A.B.I., and S.V.) and Traumatology (F.B.I.), and the Institute of Experimental Oncology and Therapy Research (A.W., D.H., and M.A.), Klinikum rechts der Isar der Technischen Universität München, Ismani.
J Bone Joint Surg Am. 2014 May 7;96(9):761-9. doi: 10.2106/JBJS.L.01794.
The aim of this controlled study was to investigate the influence of mesenchymal stem cells (MSCs) and lentiviral (LV) expression of basic fibroblast growth factor (bFGF) on tendon remodeling in an in vivo rat model of an Achilles tendon defect.
In eighty-four male Lewis rats, complete 2.4-mm tendon defects were created and were either left untreated (the phosphate-buffered saline solution [PBS] group) or were treated with mesenchymal stem cells expressing enhanced green fluorescent protein (the MSC-LV-eGFP group) or with mesenchymal stem cells expressing basic fibroblast growth factor lentivirally (the MSC-LV-bFGF group). After fourteen and twenty-eight days, the tendons were harvested and analyzed biomechanically and immunohistologically.
After fourteen days, both mesenchymal stem cell groups were slightly superior in biomechanical testing. However, only the PBS control group showed a significant increase in biomechanical results over time (fourteen versus twenty-eight days; p = 0.012). Biomechanical results were better after twenty-eight days for the control group than for both MSC groups. However, the difference was significant only with regard to the stiffness results in the comparison of the PBS control and the eGFP stem cell group (p = 0.024). Histologically, the MSC groups had no better results than the control group after fourteen and twenty-eight days. In immunohistology, only labeling for type-I procollagen was strongly increased in both MSC groups in comparison with the PBS control group (p = 0.0009 for the MSC-LV-bFGF group and p = 0.0041 for the MSC-LV-eGFP group at fourteen days, and p = 0.004 and p = 0.132, respectively, at twenty-eight days). There were no significant differences in the immunohistological results between the stem cell groups.
The biomechanical and immunohistological results showed that mesenchymal stem cells in both groups had only partially positive effects on tendon remodeling in the initial stages; however, in later stages, stem cells had potentially negative effects on biomechanical results. The additional expression of bFGF in stem cells had negligible effects on tendon remodeling.
Preliminary studies using stem cells are partially promising; however, there are no relevant clinical data showing that stem cells are of significant benefit. The present study should lead to a more critical evaluation and thoughtful use of stem cells in humans until more clinical data are available.
本对照研究旨在探讨间充质干细胞(MSCs)和慢病毒(LV)表达碱性成纤维细胞生长因子(bFGF)对体内跟腱缺损大鼠模型中腱重塑的影响。
在 84 只雄性 Lewis 大鼠中,制造了完整的 2.4mm 腱缺损,分别未治疗(磷酸盐缓冲盐水溶液 [PBS] 组)或用表达增强型绿色荧光蛋白的间充质干细胞(MSC-LV-eGFP 组)或用表达碱性成纤维细胞生长因子的间充质干细胞治疗。LV 组)。在 14 天和 28 天后,收获肌腱并进行生物力学和免疫组织化学分析。
在 14 天时,两组间充质干细胞在生物力学测试中均略有优势。然而,只有 PBS 对照组随时间推移(14 天与 28 天)显示出生物力学结果显著增加(p = 0.012)。28 天后,对照组的生物力学结果优于两组 MSC 组。然而,在 PBS 对照组与 eGFP 干细胞组的比较中,仅刚度结果的差异具有统计学意义(p = 0.024)。组织学上,14 天和 28 天后,MSC 组与对照组相比,无明显改善。免疫组织化学仅显示,与 PBS 对照组相比,两组 MSC 组的 I 型前胶原标记均明显增加(MSC-LV-bFGF 组为 p = 0.0009,MSC-LV-eGFP 组为 p = 0.0041,在 14 天,分别为 p = 0.004 和 p = 0.132,在 28 天)。两组间干细胞的免疫组织化学结果无显著差异。
生物力学和免疫组织化学结果表明,两组间充质干细胞对腱重塑的初始阶段仅有部分积极影响,但在后期阶段,干细胞对生物力学结果可能产生负面影响。干细胞中碱性成纤维细胞生长因子的额外表达对腱重塑几乎没有影响。
使用干细胞的初步研究有一定的前景,但没有相关的临床数据表明干细胞有显著的益处。本研究应导致更严格地评估和更慎重地在人类中使用干细胞,直到获得更多的临床数据。