首页> 外文OA文献 >Effects of in vivo applications of peripheral blood-derived mesenchymal stromal cells (PB-MSCs) and platlet-rich plasma (PRP) on experimentally injured deep digital flexor tendons of sheep.
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Effects of in vivo applications of peripheral blood-derived mesenchymal stromal cells (PB-MSCs) and platlet-rich plasma (PRP) on experimentally injured deep digital flexor tendons of sheep.

机译:体内应用外周血间充质基质细胞(PB-MSCs)和富血小板血浆(PRP)对实验性损伤的绵羊深指屈肌腱的影响。

摘要

Tendon injuries, degenerative tendinopathy and overuse tendinitis are common in races horses. Novel therapies aim to restore tendon functionality by means of cell-based therapy, growth factor delivery and tissue engineering approaches. This study examined the use of autologous mesenchymal stromal cells derived from peripheral blood (PB-MSCs), platelet rich plasma (PRP) and a combination of both for ameliorating experimental lesions on deep digital flexor tendons (DDFT) of Bergamasca sheep. In particular, testing the combination of blood-derived MSCs and PRP in an experimental animal model represents one of the few studies exploring a putative synergistic action of these treatments. Effectiveness of treatments was evaluated at 30 and 120 days comparing clinical, ultrasonographic and histological features together with immunohistochemical expression of collagen types 1 and 3, and cartilage oligomeric matrix protein (COMP). Significant differences were found between treated groups and their corresponding control (placebo) regarding tendon morphology and extracellular matrix (ECM) composition. However, our results indicate that the combined use of PRP and MSCs did not produce an additive or synergistic regenerative response and highlighted the predominant effect of MSCs on tendon healing, enhanced tissue remodeling and improved structural organization.
机译:肌腱损伤,退化性肌腱病和过度使用肌腱炎在赛马中很常见。新型疗法旨在通过基于细胞的疗法,生长因子递送和组织工程学方法来恢复肌腱功能。这项研究检查了使用源自外周血的自体间充质基质细胞(PB-MSC),富含血小板的血浆(PRP)以及两者的组合来改善贝尔加马斯羊深指屈肌腱(DDFT)的实验性病变。特别是,在实验动物模型中测试血液来源的MSC和PRP的组合代表了探索这些治疗的假定协同作用的少数研究之一。在30天和120天时比较了临床,超声检查和组织学特征以及1型和3型胶原蛋白以及软骨寡聚基质蛋白(COMP)的免疫组织化学表达,评估了治疗的有效性。发现治疗组与其对应的对照(安慰剂)之间在肌腱形态和细胞外基质(ECM)组成方面存在显着差异。但是,我们的结果表明,PRP和MSC的联合使用不会产生累加或协同的再生反应,并强调了MSC在肌腱愈合,增强组织重塑和改善结构组织方面的主要作用。

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